diff --git "a/annotation.jsonl" "b/annotation.jsonl" new file mode 100644--- /dev/null +++ "b/annotation.jsonl" @@ -0,0 +1,10980 @@ +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long palpebral fissure\n- Renal cortical cysts\n- Prominent fingertip pads\n- Tricuspid valve prolapse\n- Gastroesophageal reflux\n- Short stature\n- Decreased body weight\n- Tricuspid regurgitation\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypoplastic left heart syndrome"}],"image":"exported_images\/00000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- obsolete Sparse and thin eyebrow\n- Sparse eyelashes\n- Cutaneous photosensitivity\n- Poikiloderma\n- Sparse scalp hair\n- Lower-limb joint contracture\n- Lower limb muscle weakness\n- Sparse hair\n- Palmoplantar erythema\n- Abnormality on pulmonary function testing\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/00001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- High forehead\n- Low-set ears\n- Bulbous nose\n- Downslanted palpebral fissures\n- Ptosis\n- Motor delay\n- Generalized hypotonia\n- Failure to thrive\n- Mitral regurgitation\n- Patent foramen ovale\n- Abnormal cardiac ventricle morphology\n- Low posterior hairline\n- Generalized hirsutism\n- Recurrent bronchitis\n- Thoracolumbar scoliosis\n- Myopathy\n- Decreased cervical spine mobility\n- Distal arthrogryposis\n- Axial hypotonia\n- Ulnar deviation of the hand\n- Proximal placement of thumb\n- Darwin tubercle of helix\n- Nasogastric tube feeding in infancy\n- Perimembranous ventricular septal defect\n- Feeding difficulties\n- Hypoxemia\n- Clinodactyly\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Klippel-Feil syndrome"}],"image":"exported_images\/00002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Full cheeks\n- Low-set ears\n- Bulbous nose\n- Downslanted palpebral fissures\n- Ptosis\n- Delayed speech and language development\n- Osteopenia\n- Muscle weakness\n- Intrauterine growth retardation\n- Hypoglycemia\n- Delayed gross motor development\n- Short stature\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Klippel-Feil syndrome"}],"image":"exported_images\/00003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hydrocephalus\n- Micrognathia\n- Blue sclerae\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Hip dysplasia\n- Breech presentation\n- Episodic vomiting\n- Scoliosis\n- Medulloblastoma\n- Short palm\n- Cervical C2\/C3 vertebral fusion\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Klippel-Feil syndrome"}],"image":"exported_images\/00004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Microcephaly\n- Bulbous nose\n- Underdeveloped nasal alae\n- Webbed neck\n- Ptosis\n- Motor delay\n- Generalized hypotonia\n- Weak cry\n- Premature birth\n- Breech presentation\n- Low posterior hairline\n- Delayed gross motor development\n- Unsteady gait\n- Frequent falls\n- Highly arched eyebrow\n- Fused cervical vertebrae\n- Subsarcolemmal accumulations of abnormally shaped mitochondria\n- Short stature\n- Decreased body weight\n- Absent phalangeal crease\n- Bowing of the long bones\n- Type 2 muscle fiber predominance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Klippel-Feil syndrome"}],"image":"exported_images\/00005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Bulbous nose\n- Webbed neck\n- Short neck\n- Hirsutism\n- Muscle weakness\n- Bilateral ptosis\n- Intrauterine growth retardation\n- Weak voice\n- Low posterior hairline\n- Poor motor coordination\n- Hypocalcemia\n- Fused cervical vertebrae\n- Short stature\n- Decreased body weight\n- Abnormality of dental morphology\n- Feeding difficulties in infancy\n- Underdeveloped nasolabial fold\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Klippel-Feil syndrome"}],"image":"exported_images\/00006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Deeply set eye\n- Nystagmus\n- Carious teeth\n- Jaundice\n- Cutaneous photosensitivity\n- Ataxia\n- Splenomegaly\n- Vomiting\n- Diarrhea\n- Intention tremor\n- Hepatomegaly\n- Progressive neurologic deterioration\n- Abnormal cerebral white matter morphology\n- Inability to walk\n- Elevated hepatic transaminase\n- Short stature\n- Decreased body weight\n- Absent patellar reflexes\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME A; CSA"}],"image":"exported_images\/00007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Deeply set eye\n- Cataract\n- Pigmentary retinopathy\n- Carious teeth\n- Ataxia\n- Mental deterioration\n- Progressive neurologic deterioration\n- Elevated hepatic transaminase\n- Peripheral axonal neuropathy\n- Difficulty standing\n- Short stature\n- Decreased body weight\n- Severe postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME A; CSA"}],"image":"exported_images\/00008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Sparse eyelashes\n- Delayed puberty\n- Hypohidrosis\n- Poikiloderma\n- Muscle weakness\n- Growth delay\n- Dysphagia\n- Restrictive ventilatory defect\n- Sparse scalp hair\n- Loss of ambulation\n- Areflexia of lower limbs\n- Scoliosis\n- Respiratory insufficiency due to muscle weakness\n- Myopathy\n- Skeletal muscle atrophy\n- Muscular dystrophy\n- Involuntary movements\n- Lower-limb joint contracture\n- Sparse hair\n- Mildly elevated creatine kinase\n- Fatty replacement of skeletal muscle\n- Reduced muscle fiber calpain-3\n- Skeletal muscle fibrosis\n- Sparse eyebrow\n- Upper-limb joint contracture\n- Sclerosis of finger phalanx\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/00009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Macrotia\n- Delayed speech and language development\n- Short stature\n- Decreased body weight\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Intellectual disability, severe\n- Delayed social development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72; MRT72"}],"image":"exported_images\/00010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Low-set, posteriorly rotated ears\n- Prominent nose\n- Broad nasal tip\n- Autistic behavior\n- Self-mutilation\n- Spasticity\n- Global developmental delay\n- Absent speech\n- Tachycardia\n- Nonimmune hydrops fetalis\n- Truncal ataxia\n- Gait imbalance\n- Decreased body weight\n- Intellectual disability, severe\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72; MRT72"}],"image":"exported_images\/00011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Low-set, posteriorly rotated ears\n- Prominent nose\n- Broad nasal tip\n- Autistic behavior\n- Self-mutilation\n- Delayed speech and language development\n- Spasticity\n- Global developmental delay\n- Atrial septal defect\n- Pulmonic stenosis\n- Truncal ataxia\n- Short stature\n- Decreased body weight\n- Intellectual disability, severe\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72; MRT72"}],"image":"exported_images\/00012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Inguinal hernia\n- Cryptorchidism\n- Hypospadias\n- Hydrocephalus\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Posteriorly rotated ears\n- Abnormal retinal morphology\n- Dental crowding\n- Delayed speech and language development\n- Single transverse palmar crease\n- Single umbilical artery\n- Abnormal fingertip morphology\n- Hypotonia\n- Dysarthria\n- Motor delay\n- Abnormal corpus callosum morphology\n- Abnormal cerebellum morphology\n- Flexion contracture\n- Bilateral ptosis\n- Umbilical hernia\n- Diastasis recti\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Overlapping toe\n- Constipation\n- Respiratory distress\n- Low posterior hairline\n- Choroid plexus cyst\n- Hepatomegaly\n- Drooling\n- Abnormal venous morphology\n- Inverted nipples\n- Renal malrotation\n- Agenesis of permanent teeth\n- Wide intermamillary distance\n- Lower limb hypertonia\n- Attention deficit hyperactivity disorder\n- Bilateral sensorineural hearing impairment\n- Feeding difficulties in infancy\n- Stridor\n- Overlapping fingers\n- Abnormal number of hair whorls\n- Right bundle branch block\n- Flat face\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD"}],"image":"exported_images\/00013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Proteinuria\n- Thick lower lip vermilion\n- High palate\n- Everted lower lip vermilion\n- Microcephaly\n- Narrow face\n- Long face\n- Coarse facial features\n- Short philtrum\n- Conductive hearing impairment\n- Sensorineural hearing impairment\n- Optic atrophy\n- Compulsive behaviors\n- Delayed speech and language development\n- Abnormal sternum morphology\n- Edema\n- Intellectual disability\n- Seizure\n- Motor delay\n- Flexion contracture\n- Joint hypermobility\n- Delayed closure of the anterior fontanelle\n- Atrial septal defect\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Aortic regurgitation\n- Overlapping toe\n- Tethered cord\n- Pulmonary embolism\n- Motor deterioration\n- Poor speech\n- Scoliosis\n- Osteoarthritis\n- Meningioma\n- Abnormality of tibia morphology\n- Hyperlipidemia\n- Arterial calcification\n- Syringomyelia\n- Short stature\n- Cranial nerve paralysis\n- Lower limb muscle weakness\n- Pes valgus\n- Superiorly displaced ears\n- Feeding difficulties in infancy\n- Leg muscle stiffness\n- Overlapping fingers\n- Protruding tongue\n- Avascular necrosis\n- Joint subluxation\n- Narrow palpebral fissure\n- Hypersomnia\n- Recurrent ear infections\n- Cerebral infarct\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD"}],"image":"exported_images\/00014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Parietal bossing\n- Trigonocephaly\n- Epicanthus\n- Low anterior hairline\n- Pointed chin\n- High forehead\n- Cystic hygroma\n- Deeply set eye\n- Ptosis\n- Carious teeth\n- Atypical behavior\n- Autism\n- Jaundice\n- Syndactyly\n- Prominent fingertip pads\n- Small thenar eminence\n- Seizure\n- Absent speech\n- Intrauterine growth retardation\n- Pes planus\n- Sandal gap\n- Clinodactyly of the 5th toe\n- Frontal bossing\n- Constipation\n- Developmental regression\n- Abnormal venous morphology\n- Cubitus valgus\n- Inverted nipples\n- Metacarpophalangeal joint hyperextensibility\n- Wide intermamillary distance\n- Attention deficit hyperactivity disorder\n- Excessive wrinkling of palmar skin\n- Pes valgus\n- Proximal placement of thumb\n- Broad hallux\n- Small hypothenar eminence\n- Abnormality of the palmar creases\n- Abnormal number of hair whorls\n- Clinodactyly of the 4th toe\n- Feeding difficulties\n- Abnormal lateral ventricle morphology\n- Clinodactyly\n- Motor regression\n- Hypersomnia\n- Infra-orbital crease\n- Abnormal jugular vein morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD"}],"image":"exported_images\/00015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Trigonocephaly\n- Epicanthus\n- Low-set ears\n- Broad nasal tip\n- Ptosis\n- Pseudopapilledema\n- Pectus carinatum\n- Missing ribs\n- Sacral dimple\n- Global developmental delay\n- Cerebellar atrophy\n- Umbilical hernia\n- Right ventricular hypertrophy\n- Double outlet right ventricle\n- Deep plantar creases\n- Abnormal bleeding\n- Cerebral atrophy\n- Tethered cord\n- Curly hair\n- Neonatal respiratory distress\n- Inverted nipples\n- Hypoplastic left heart\n- Pulmonary artery atresia\n- Depressed nasal bridge\n- Redundant neck skin\n- Deep palmar crease\n- Sparse hair\n- Long toe\n- Prominent forehead\n- Broad eyebrow\n- Feeding difficulties\n- Systolic heart murmur\n- Sparse eyebrow\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD"}],"image":"exported_images\/00016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Narrow forehead\n- Small forehead\n- Anteverted nares\n- Neonatal insulin-dependent diabetes mellitus\n- Osteopenia\n- Jaundice\n- Seizure\n- Agenesis of corpus callosum\n- Generalized hypotonia\n- Cerebellar vermis hypoplasia\n- Pneumonia\n- Intellectual disability, profound\n- Recurrent respiratory infections\n- Lower limb hyperreflexia\n- Scoliosis\n- High, narrow palate\n- Pathologic fracture\n- Hyperglycemia\n- Slender long bone\n- Short stature\n- Decreased body weight\n- Axial hypotonia\n- Simplified gyral pattern\n- Tented upper lip vermilion\n- EEG with burst suppression\n- EEG with generalized sharp slow waves\n- Feeding difficulties\n- Infantile spasms\n- Profound global developmental delay\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, epilepsy, and diabetes syndrome"}],"image":"exported_images\/00017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Open mouth\n- Gingival overgrowth\n- Microcephaly\n- Full cheeks\n- Narrow forehead\n- Small forehead\n- Anteverted nares\n- Optic atrophy\n- Neonatal insulin-dependent diabetes mellitus\n- Osteopenia\n- Edema\n- Lethargy\n- Agenesis of corpus callosum\n- Myoclonus\n- Brisk reflexes\n- Cerebral atrophy\n- Scoliosis\n- High, narrow palate\n- Ketonuria\n- Hyperglycemia\n- Slender long bone\n- Clinodactyly of the 5th finger\n- Respiratory infections in early life\n- Axial hypotonia\n- Simplified gyral pattern\n- Tented upper lip vermilion\n- EEG with burst suppression\n- Infantile spasms\n- Albuminuria\n- Profound global developmental delay\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, epilepsy, and diabetes syndrome"}],"image":"exported_images\/00018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Microcephaly\n- Full cheeks\n- Narrow forehead\n- Small forehead\n- Anteverted nares\n- Neonatal insulin-dependent diabetes mellitus\n- Osteopenia\n- Jaundice\n- Agenesis of corpus callosum\n- Myoclonus\n- Scoliosis\n- High, narrow palate\n- Hyperglycemia\n- Slender long bone\n- Simplified gyral pattern\n- Tented upper lip vermilion\n- EEG with burst suppression\n- Infantile spasms\n- Profound global developmental delay\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, epilepsy, and diabetes syndrome"}],"image":"exported_images\/00019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Horseshoe kidney\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Bulbous nose\n- Visual impairment\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Decreased response to growth hormone stimulation test\n- Seizure\n- Hypotonia\n- Cerebellar atrophy\n- Abnormal corpus callosum morphology\n- Absent speech\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Abnormal caudate nucleus morphology\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Sparse lateral eyebrow\n- Bilateral single transverse palmar creases\n- Mild neurosensory hearing impairment\n- Anterior pituitary hypoplasia\n- Intellectual disability, severe\n- Severe global developmental delay\n- Infantile spasms\n- Unilateral cryptorchidism\n- Exodeviation\n- Mild myopia\n- Sleep onset insomnia\n- Maintenance insomnia\n- Mild hypermetropia\n- Unilateral cleft lip\n- Unilateral cleft palate\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB"}],"image":"exported_images\/00020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- High palate\n- Microcephaly\n- Epicanthus\n- Round face\n- Anteverted nares\n- Atypical behavior\n- Dandy-Walker malformation\n- Umbilical hernia\n- Ventricular septal defect\n- Pulmonic stenosis\n- Dysphagia\n- Bilateral tonic-clonic seizure\n- Polymicrogyria\n- Dilated fourth ventricle\n- Sleep disturbance\n- Downturned corners of mouth\n- Aspiration\n- Clinodactyly of the 5th finger\n- Short stature\n- Dysplastic pulmonary valve\n- Depressed nasal bridge\n- Mild conductive hearing impairment\n- Epiblepharon\n- Severe global developmental delay\n- Feeding difficulties\n- Head-banging\n- Flat face\n- Frequent temper tantrums\n- Sleep onset insomnia\n- Maintenance insomnia\n- Myoclonic seizure\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB"}],"image":"exported_images\/00021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Strabismus\n- Hypermetropia\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Craniosynostosis\n- Atrial septal defect\n- Patent foramen ovale\n- Poor suck\n- Sleep disturbance\n- Supernumerary nipple\n- Decreased body weight\n- 2-3 toe syndactyly\n- Asymmetry of the ears\n- Feeding difficulties\n- Unilateral cryptorchidism\n- obsolete Psychomotor retardation\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES; IDDILF"}],"image":"exported_images\/00022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Facial asymmetry\n- Abnormal repetitive mannerisms\n- Short attention span\n- Anxiety\n- Delayed speech and language development\n- Eczema\n- Cutaneous photosensitivity\n- Striae distensae\n- Tapered finger\n- Intellectual disability\n- Global developmental delay\n- Gait disturbance\n- Large for gestational age\n- Pes planus\n- Truncal obesity\n- Neonatal hypoglycemia\n- Constipation\n- Abdominal pain\n- Incoordination\n- Expressive language delay\n- Highly arched eyebrow\n- Elevated hepatic transaminase\n- Hyposmia\n- Accelerated skeletal maturation\n- Anisocoria\n- Tip-toe gait\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES; IDDILF"}],"image":"exported_images\/00023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Delayed cranial suture closure\n- Epicanthus\n- Short philtrum\n- Narrow forehead\n- High forehead\n- Overfolded helix\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Telecanthus\n- Hypermetropia\n- Amblyopia\n- Delayed speech and language development\n- Tapered finger\n- Single umbilical artery\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Hip dysplasia\n- Joint laxity\n- Obesity\n- Patent foramen ovale\n- Pes planus\n- Overlapping toe\n- Frontal bossing\n- Constipation\n- Delayed CNS myelination\n- Difficulty walking\n- Scoliosis\n- Short nose\n- Pes valgus\n- Feeding difficulties in infancy\n- Feeding difficulties\n- Heart murmur\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES; IDDILF"}],"image":"exported_images\/00024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Full cheeks\n- Low anterior hairline\n- Smooth philtrum\n- Short philtrum\n- Narrow forehead\n- Low-set ears\n- Protruding ear\n- Broad nasal tip\n- Anteverted nares\n- Telecanthus\n- Long eyelashes\n- Periorbital fullness\n- Horizontal nystagmus\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Cerebral atrophy\n- Low posterior hairline\n- Hypsarrhythmia\n- Vertical nystagmus\n- Multifocal epileptiform discharges\n- Hypoplasia of the pons\n- Visual fixation instability\n- Tonic seizure\n- Myoclonic seizure\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23; DEE23"}],"image":"exported_images\/00025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Full cheeks\n- Low anterior hairline\n- Smooth philtrum\n- Short philtrum\n- Low-set ears\n- Protruding ear\n- Broad nasal tip\n- Anteverted nares\n- Telecanthus\n- Long eyelashes\n- Periorbital fullness\n- Horizontal nystagmus\n- Delayed speech and language development\n- Cerebellar atrophy\n- Atrial septal defect\n- Cerebral atrophy\n- Low posterior hairline\n- Hypsarrhythmia\n- Vertical nystagmus\n- Atonic seizure\n- Multifocal epileptiform discharges\n- Hypoplasia of the pons\n- Visual fixation instability\n- Tonic seizure\n- Myoclonic seizure\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23; DEE23"}],"image":"exported_images\/00026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Choreoathetosis\n- Hyperreflexia\n- Lower limb spasticity\n- Axial hypotonia\n- Intellectual disability, severe\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 58; MRT58"}],"image":"exported_images\/00027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Low anterior hairline\n- Broad nasal tip\n- Anteverted nares\n- Telecanthus\n- Periorbital fullness\n- Autistic behavior\n- Reduced eye contact\n- Absent speech\n- Bicuspid aortic valve\n- Motor deterioration\n- Hypsarrhythmia\n- Supravalvular aortic stenosis\n- Hypoplasia of the pons\n- Infantile spasms\n- Cerebral white matter atrophy\n- Heart murmur\n- Tonic seizure\n- Short corpus callosum\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23; DEE23"}],"image":"exported_images\/00028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Low anterior hairline\n- Broad nasal tip\n- Anteverted nares\n- Telecanthus\n- Periorbital fullness\n- Motor delay\n- Myoclonus\n- Hypoplasia of the corpus callosum\n- Focal impaired awareness seizure\n- Atonic seizure\n- Interictal epileptiform activity\n- EEG with focal epileptiform discharges\n- Tonic seizure\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23; DEE23"}],"image":"exported_images\/00029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Xerostomia\n- High palate\n- Narrow forehead\n- Protruding ear\n- Strabismus\n- Ptosis\n- Diplopia\n- Oligodontia\n- Delayed speech and language development\n- Hypergonadotropic hypogonadism\n- Intellectual disability, mild\n- Dysarthria\n- Neonatal hypotonia\n- Muscle weakness\n- Hypernasal speech\n- Gastroesophageal reflux\n- Poor suck\n- Myopathic facies\n- Neonatal respiratory distress\n- Proximal muscle weakness\n- Neck flexor weakness\n- Feeding difficulties in infancy\n- Overweight\n- Weakness of facial musculature\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22"}],"image":"exported_images\/00030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Ectropion\n- Conical tooth\n- Abnormal hair morphology\n- Nail dysplasia\n- Distichiasis\n- Tooth agenesis\n- Euryblepharon\n- Lagophthalmos\n- Neural tube defect\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Facial asymmetry\n- Posteriorly rotated ears\n- Overfolded helix\n- Choanal atresia\n- Microphthalmia\n- Upslanted palpebral fissure\n- Blindness\n- Global developmental delay\n- Agenesis of corpus callosum\n- Abnormal heart morphology\n- Tetralogy of Fallot\n- Bilateral cleft lip and palate\n- Meningoencephalocele\n- Opacification of the corneal stroma\n- Teratoma\n- Fused lumbar vertebrae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Hearing impairment\n- Sensorineural hearing impairment\n- Upslanted palpebral fissure\n- Blue sclerae\n- Joint laxity\n- Umbilical hernia\n- Attention deficit hyperactivity disorder\n- Mild global developmental delay\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Thin vermilion border\n- Microcephaly\n- Retrognathia\n- Narrow forehead\n- Nystagmus\n- Failure to thrive\n- Atrial septal defect\n- Patent ductus arteriosus\n- Ventriculomegaly\n- EEG abnormality\n- Cavum septum pellucidum\n- Short stature\n- Prominent nasal tip\n- Aplasia\/Hypoplasia of the cerebellar vermis\n- Sparse hair\n- Prominent forehead\n- Severe global developmental delay\n- Overhanging nasal tip\n- Narrow palpebral fissure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MAPKAPK5"}],"image":"exported_images\/00034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin vermilion border\n- Microcephaly\n- Retrognathia\n- Sensorineural hearing impairment\n- Cataract\n- Nystagmus\n- Sclerocornea\n- Syndactyly\n- Hand polydactyly\n- Abnormal heart morphology\n- Hypoplasia of the corpus callosum\n- Uplifted earlobe\n- Severe global developmental delay\n- Double inlet left ventricle\n- Congenital malformation of the great arteries\n- Short palpebral fissure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MAPKAPK5"}],"image":"exported_images\/00035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Bifid uvula\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Abnormality of the ear\n- Intellectual disability\n- Global developmental delay\n- Stroke\n- Ventriculomegaly\n- Accelerated skeletal maturation\n- Moyamoya phenomenon\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/00036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Low-set ears\n- Cupped ear\n- Intellectual disability\n- Global developmental delay\n- Ventriculomegaly\n- Fused cervical vertebrae\n- Chiari type I malformation\n- Microtia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/00037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Open mouth\n- High palate\n- Long face\n- Oval face\n- Protruding ear\n- Strabismus\n- Ptosis\n- Proptosis\n- Myopia\n- Pectus excavatum\n- Multiple lentigines\n- Joint laxity\n- Atrial septal defect\n- Overlapping toe\n- Moderate global developmental delay\n- Thick vermilion border\n- Camptodactyly of finger\n- Type I diabetes mellitus\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51"}],"image":"exported_images\/00038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Square face\n- Prominent nasal bridge\n- Strabismus\n- Downslanted palpebral fissures\n- Myopia\n- Specific learning disability\n- Atrial septal defect\n- Moderate global developmental delay\n- Feeding difficulties\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 65; MRT65"}],"image":"exported_images\/00039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Visual impairment\n- Ptosis\n- Myopia\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Attention deficit hyperactivity disorder\n- Moderate sensorineural hearing impairment\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA"}],"image":"exported_images\/00040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Autistic behavior\n- Hypotonia\n- Motor delay\n- Ventricular septal defect\n- Pyloric stenosis\n- Intellectual disability, moderate\n- Sleep disturbance\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Metopic synostosis\n- Double orifice mitral valve\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA"}],"image":"exported_images\/00041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypotonia\n- Motor delay\n- Intellectual disability, moderate\n- Conspicuously happy disposition\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA"}],"image":"exported_images\/00042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ptosis\n- Myopia\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Episodic vomiting\n- Attention deficit hyperactivity disorder\n- Glue ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA"}],"image":"exported_images\/00043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Bifid scrotum\n- Hypoplastic male external genitalia\n- Brachycephaly\n- Bulbous nose\n- Wide nose\n- Proptosis\n- Thick eyebrow\n- Intellectual disability\n- Midface retrusion\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/00044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypertelorism\n- Facial asymmetry\n- Bulbous nose\n- Wide nose\n- Proptosis\n- Thick eyebrow\n- Upper eyelid coloboma\n- Intellectual disability\n- Midface retrusion\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/00045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypertelorism\n- Facial asymmetry\n- Bulbous nose\n- Wide nose\n- Proptosis\n- Thick eyebrow\n- Upper eyelid coloboma\n- Intellectual disability\n- Midface retrusion\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/00046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Microcephaly\n- Choanal atresia\n- Iris coloboma\n- Global developmental delay\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Small nail\n- Ventriculomegaly\n- Clinodactyly of the 5th finger\n- Short stature\n- Anomalous pulmonary venous return\n- Simple ear\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART; NEDBEH"}],"image":"exported_images\/00047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Furrowed tongue\n- Epicanthus\n- Deeply set eye\n- Atypical behavior\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Cerebellar vermis hypoplasia\n- Hip dysplasia\n- Hypoglycemia\n- Intellectual disability, moderate\n- Temperature instability\n- Bilateral single transverse palmar creases\n- Broad thumb\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART; NEDBEH"}],"image":"exported_images\/00048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Broad philtrum\n- Triangular face\n- Proptosis\n- Synophrys\n- Autistic behavior\n- Seizure\n- Generalized hypotonia\n- Specific learning disability\n- Frontal bossing\n- Inverted nipples\n- Microtia\n- Large earlobe\n- Prominent forehead\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51"}],"image":"exported_images\/00049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Broad philtrum\n- Triangular face\n- Proptosis\n- Synophrys\n- Autistic behavior\n- Seizure\n- Generalized hypotonia\n- Specific learning disability\n- Frontal bossing\n- Inverted nipples\n- Microtia\n- Large earlobe\n- Prominent forehead\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51"}],"image":"exported_images\/00050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Failure to thrive\n- Ventriculomegaly\n- Intellectual disability, profound\n- Sleep disturbance\n- Secondary microcephaly\n- Lamellar cataract\n- Feeding difficulties\n- Delayed myelination\n- Infantile spasms\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM"}],"image":"exported_images\/00051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cataract\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Irritability\n- Dysphagia\n- Intellectual disability, profound\n- Secondary microcephaly\n- Focal-onset seizure\n- Brain atrophy\n- Profound global developmental delay\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM"}],"image":"exported_images\/00052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Developmental cataract\n- Irritability\n- Hypotonia\n- Failure to thrive\n- Intellectual disability, profound\n- Sleep disturbance\n- Secondary microcephaly\n- Anterior subcapsular cataract\n- Feeding difficulties\n- Delayed myelination\n- Infantile spasms\n- Profound global developmental delay\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM"}],"image":"exported_images\/00053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Irritability\n- Failure to thrive\n- Dysphagia\n- Intellectual disability, profound\n- Infantile spasms\n- Profound global developmental delay\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM"}],"image":"exported_images\/00054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Autistic behavior\n- Irritability\n- Gastroesophageal reflux\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Abnormal cerebral white matter morphology\n- Obstructive sleep apnea\n- Intellectual disability, severe\n- Severe global developmental delay\n- Feeding difficulties\n- Hyperintensity of cerebral white matter on MRI\n- Nocturnal seizures\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM"}],"image":"exported_images\/00055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Hypotonia\n- Cerebellar atrophy\n- Reduced tendon reflexes\n- Laryngomalacia\n- Anal atresia\n- Limb hypertonia\n- Thoracic scoliosis\n- Corpus callosum atrophy\n- Axial hypotonia\n- Severe global developmental delay\n- Abnormal sixth cranial nerve morphology\n- Multifocal seizures\n- Cerebral visual impairment\n- Hippocampal sclerosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR"}],"image":"exported_images\/00056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Retrognathia\n- Short philtrum\n- Deeply set eye\n- Abnormal electroretinogram\n- Abnormality of visual evoked potentials\n- Delayed speech and language development\n- Prominent fingertip pads\n- Global developmental delay\n- Cerebellar atrophy\n- Reduced tendon reflexes\n- Cerebral atrophy\n- Limb hypertonia\n- Scoliosis\n- Secondary microcephaly\n- Corpus callosum atrophy\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR"}],"image":"exported_images\/00057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Retrognathia\n- Short philtrum\n- Deeply set eye\n- Abnormal electroretinogram\n- Abnormality of visual evoked potentials\n- Delayed speech and language development\n- Prominent fingertip pads\n- Global developmental delay\n- Cerebellar atrophy\n- Reduced tendon reflexes\n- Cerebral atrophy\n- Limb hypertonia\n- Scoliosis\n- Secondary microcephaly\n- Corpus callosum atrophy\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR"}],"image":"exported_images\/00058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Deeply set eye\n- Delayed speech and language development\n- Mild global developmental delay\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR"}],"image":"exported_images\/00059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Abnormal cerebellum morphology\n- Plagiocephaly\n- Joint laxity\n- Mitral regurgitation\n- Aortic regurgitation\n- Short foot\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Intellectual disability, moderate\n- Abnormal cerebral white matter morphology\n- Scoliosis\n- Short palm\n- Tricuspid regurgitation\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Pulmonary insufficiency\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48"}],"image":"exported_images\/00060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hyperactivity\n- Eczema\n- Intellectual disability, mild\n- Abnormal cerebellum morphology\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Intellectual disability, moderate\n- Recurrent pneumonia\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48"}],"image":"exported_images\/00061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypospadias\n- Visual impairment\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Ventricular septal defect\n- Hypoplasia of the corpus callosum\n- Polymicrogyria\n- Sleep disturbance\n- Congenital sensorineural hearing impairment\n- Abnormality of the palmar creases\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48"}],"image":"exported_images\/00062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Intellectual disability, moderate\n- Abnormal cerebral white matter morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48"}],"image":"exported_images\/00063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Recurrent otitis media\n- Autism\n- Abnormal repetitive mannerisms\n- Eczema\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Absent speech\n- Abnormal cerebral white matter morphology\n- Increased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48"}],"image":"exported_images\/00064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long face\n- Retrognathia\n- Coarse facial features\n- Mandibular prognathia\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Telecanthus\n- Proptosis\n- Thick eyebrow\n- Cutis laxa\n- Prominent superficial veins\n- Limited elbow extension\n- Small for gestational age\n- Short toe\n- Sandal gap\n- Highly arched eyebrow\n- Sclerosis of skull base\n- Hip dislocation\n- Severe short stature\n- Decreased body weight\n- Deep palmar crease\n- Excessive wrinkled skin\n- Lipodystrophy\n- Short finger\n- Severe global developmental delay\n- Broad chin\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long face\n- Retrognathia\n- Coarse facial features\n- Mandibular prognathia\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Telecanthus\n- Proptosis\n- Thick eyebrow\n- Cutis laxa\n- Prominent superficial veins\n- Limited elbow extension\n- Small for gestational age\n- Short toe\n- Sandal gap\n- Highly arched eyebrow\n- Sclerosis of skull base\n- Hip dislocation\n- Severe short stature\n- Decreased body weight\n- Deep palmar crease\n- Excessive wrinkled skin\n- Lipodystrophy\n- Short finger\n- Severe global developmental delay\n- Broad chin\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long face\n- Retrognathia\n- Coarse facial features\n- Mandibular prognathia\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Telecanthus\n- Proptosis\n- Thick eyebrow\n- Cutis laxa\n- Prominent superficial veins\n- Limited elbow extension\n- Small for gestational age\n- Short toe\n- Sandal gap\n- Highly arched eyebrow\n- Sclerosis of skull base\n- Hip dislocation\n- Severe short stature\n- Decreased body weight\n- Deep palmar crease\n- Excessive wrinkled skin\n- Lipodystrophy\n- Short finger\n- Severe global developmental delay\n- Broad chin\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Large fontanelles\n- Microcephaly\n- Retrognathia\n- Long philtrum\n- Telecanthus\n- Brachydactyly\n- Patent foramen ovale\n- Downturned corners of mouth\n- Symphalangism of the 4th finger\n- Symphalangism of the 5th finger\n- Progeroid facial appearance\n- Excessive wrinkled skin\n- Short finger\n- Mild global developmental delay\n- Clinodactyly\n- Fetal nuchal edema\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Large fontanelles\n- Microcephaly\n- Retrognathia\n- Long philtrum\n- Telecanthus\n- Brachydactyly\n- Patent foramen ovale\n- Downturned corners of mouth\n- Symphalangism of the 4th finger\n- Symphalangism of the 5th finger\n- Progeroid facial appearance\n- Excessive wrinkled skin\n- Short finger\n- Mild global developmental delay\n- Clinodactyly\n- Fetal nuchal edema\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long face\n- Retrognathia\n- Coarse facial features\n- Mandibular prognathia\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Telecanthus\n- Proptosis\n- Thick eyebrow\n- Cutis laxa\n- Prominent superficial veins\n- Limited elbow extension\n- Small for gestational age\n- Short toe\n- Sandal gap\n- Highly arched eyebrow\n- Sclerosis of skull base\n- Hip dislocation\n- Severe short stature\n- Decreased body weight\n- Deep palmar crease\n- Excessive wrinkled skin\n- Lipodystrophy\n- Short finger\n- Severe global developmental delay\n- Broad chin\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micropenis\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Seizure\n- Limited elbow movement\n- Short long bone\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Short humerus\n- Rhizomelia\n- Limb undergrowth\n- Hypoplastic nasal bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Omodysplasia"}],"image":"exported_images\/00071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocephalus\n- Seizure\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Failure to thrive\n- Enlarged cisterna magna\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KCTD3"}],"image":"exported_images\/00072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Thin upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Abnormality of the ear\n- Delayed speech and language development\n- Delayed gross motor development\n- Language impairment\n- Increased body weight\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Abnormality of the palpebral fissures\n- High anterior hairline\n- Thick nasal alae\n- Delayed fine motor development\n- Intellectual disability, severe\n- Narrow jaw\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF"}],"image":"exported_images\/00073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Abnormality of the ear\n- Autistic behavior\n- Delayed gross motor development\n- Language impairment\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Abnormality of the palpebral fissures\n- Thick nasal alae\n- Delayed fine motor development\n- Intellectual disability, severe\n- Narrow jaw\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF"}],"image":"exported_images\/00074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Thin upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Abnormality of the ear\n- Delayed speech and language development\n- Tapered finger\n- Pes planus\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Increased body weight\n- Abnormality of the palpebral fissures\n- High anterior hairline\n- Thick nasal alae\n- Delayed fine motor development\n- Narrow jaw\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF"}],"image":"exported_images\/00075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Cerebellar vermis atrophy\n- Periventricular cysts\n- Posterior fossa cyst\n- Encephalomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KCTD3"}],"image":"exported_images\/00076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Abnormality of vision\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Cerebellar hypoplasia\n- Patent foramen ovale\n- Myopathic facies\n- Ventriculomegaly\n- Hypsarrhythmia\n- Hip dislocation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KCTD3"}],"image":"exported_images\/00077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocephalus\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Myopathic facies\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Cavum septum pellucidum\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KCTD3"}],"image":"exported_images\/00078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Low-set ears\n- Wide nasal bridge\n- Short neck\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Increased body weight\n- Intellectual disability, borderline\n- Localized skin lesion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Low-set ears\n- Wide nasal bridge\n- Short neck\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Increased body weight\n- Intellectual disability, borderline\n- Localized skin lesion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Low-set ears\n- Wide nasal bridge\n- Short neck\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Increased body weight\n- Intellectual disability, borderline\n- Localized skin lesion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Low-set ears\n- Wide nasal bridge\n- Short neck\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Increased body weight\n- Intellectual disability, borderline\n- Localized skin lesion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Gingival overgrowth\n- Underdeveloped nasal alae\n- Proptosis\n- Spastic tetraparesis\n- Polyhydramnios\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Absence of subcutaneous fat\n- Lipodystrophy\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEPPEN-LUBINSKY SYNDROME; KPLBS"}],"image":"exported_images\/00083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Global developmental delay\n- Respiratory distress\n- Ventriculomegaly\n- Opisthotonus\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Upper airway obstruction\n- Reduced subcutaneous adipose tissue\n- Short stature\n- Decreased body weight\n- Narrow naris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEPPEN-LUBINSKY SYNDROME; KPLBS"}],"image":"exported_images\/00084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Ambiguous genitalia\n- Micrognathia\n- Myopia\n- Hypotelorism\n- Autism\n- Penoscrotal hypospadias\n- Seizure\n- Global developmental delay\n- Joint laxity\n- Intrauterine growth retardation\n- Small for gestational age\n- Gastroesophageal reflux\n- Language impairment\n- Obstructive sleep apnea\n- Scaphocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY; SRMMD"}],"image":"exported_images\/00085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Small scrotum\n- Micropenis\n- Microcephaly\n- Micrognathia\n- Cataract\n- Hypotelorism\n- Short diaphyses\n- Large hands\n- Intellectual disability, mild\n- Intrauterine growth retardation\n- Small for gestational age\n- Broad foot\n- Coxa valga\n- Bowing of the legs\n- Skeletal muscle hypertrophy\n- Advanced ossification of the hand bones\n- Short stature\n- Short lower limbs\n- Rhizomelia\n- Primary microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY; SRMMD"}],"image":"exported_images\/00086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Micrognathia\n- Hypotelorism\n- Global developmental delay\n- Cerebellar atrophy\n- Joint laxity\n- Intrauterine growth retardation\n- Delayed CNS myelination\n- Skeletal muscle hypertrophy\n- Short stature\n- Decreased body weight\n- Postnatal growth retardation\n- Rhizomelia\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY; SRMMD"}],"image":"exported_images\/00087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Polyuria\n- Aggressive behavior\n- Seizure\n- Ataxia\n- Hypotonia\n- Delayed gross motor development\n- Sleep disturbance\n- Expressive language delay\n- Short stature\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 46; MRT46"}],"image":"exported_images\/00088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Aggressive behavior\n- Seizure\n- Large for gestational age\n- Delayed gross motor development\n- Expressive language delay\n- Short stature\n- Intellectual disability, severe\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 46; MRT46"}],"image":"exported_images\/00089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Strabismus\n- Irritability\n- Seizure\n- Slurred speech\n- Large for gestational age\n- Pes planus\n- Delayed gross motor development\n- Expressive language delay\n- Short stature\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 46; MRT46"}],"image":"exported_images\/00090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Macrotia\n- Protruding ear\n- Hypotonia\n- Pes planus\n- Ventriculomegaly\n- Delayed gross motor development\n- Expressive language delay\n- Delayed fine motor development\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 46; MRT46"}],"image":"exported_images\/00091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Tall stature\n- Abnormality of the genitourinary system\n- Macrocephaly\n- Overfolded helix\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hematuria\n- Reduced eye contact\n- Jaundice\n- Cutis marmorata\n- Hypotonia\n- Failure to thrive\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Delayed gross motor development\n- Delayed fine motor development\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD"}],"image":"exported_images\/00092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Tall stature\n- Abnormality of the genitourinary system\n- Macrocephaly\n- Overfolded helix\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hematuria\n- Reduced eye contact\n- Jaundice\n- Cutis marmorata\n- Hypotonia\n- Failure to thrive\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Delayed gross motor development\n- Delayed fine motor development\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD"}],"image":"exported_images\/00093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Tall stature\n- Abnormality of the genitourinary system\n- Macrocephaly\n- Overfolded helix\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hematuria\n- Reduced eye contact\n- Jaundice\n- Cutis marmorata\n- Hypotonia\n- Failure to thrive\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Delayed gross motor development\n- Delayed fine motor development\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD"}],"image":"exported_images\/00094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Tall stature\n- Abnormality of the genitourinary system\n- Macrocephaly\n- Overfolded helix\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hematuria\n- Reduced eye contact\n- Jaundice\n- Cutis marmorata\n- Hypotonia\n- Failure to thrive\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Delayed gross motor development\n- Delayed fine motor development\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD"}],"image":"exported_images\/00095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Tall stature\n- Abnormality of the genitourinary system\n- Macrocephaly\n- Overfolded helix\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hematuria\n- Reduced eye contact\n- Jaundice\n- Cutis marmorata\n- Hypotonia\n- Failure to thrive\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Delayed gross motor development\n- Delayed fine motor development\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD"}],"image":"exported_images\/00096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Jaundice\n- Hypotonia\n- Splenomegaly\n- Diarrhea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Jaundice\n- Hypotonia\n- Splenomegaly\n- Diarrhea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Otitis media\n- Pneumonia\n- Asthma\n- Crusting erythematous dermatitis\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Asthma\n- Crusting erythematous dermatitis\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Intellectual disability, profound\n- Abnormal muscle tone\n- Intellectual disability, severe\n- Feeding difficulties\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES; NEDBAF"}],"image":"exported_images\/00102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Global developmental delay\n- Intellectual disability, profound\n- Abnormal muscle tone\n- Intellectual disability, severe\n- Feeding difficulties\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES; NEDBAF"}],"image":"exported_images\/00103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Global developmental delay\n- Intellectual disability, profound\n- Abnormal muscle tone\n- Intellectual disability, severe\n- Feeding difficulties\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES; NEDBAF"}],"image":"exported_images\/00104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Optic atrophy\n- Horizontal nystagmus\n- Tapered finger\n- Seizure\n- Spasticity\n- Dystonia\n- Absent speech\n- Hip dysplasia\n- Broad-based gait\n- Intellectual disability, profound\n- Bruxism\n- Intellectual disability, severe\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW"}],"image":"exported_images\/00105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Narrow chest\n- Thin ribs\n- Osteopenia\n- Motor delay\n- Neonatal hypotonia\n- Small for gestational age\n- Overlapping toe\n- Short columella\n- Hypoplasia of the corpus callosum\n- Highly arched eyebrow\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Microtia\n- Feeding difficulties\n- Flat face\n- Camptodactyly\n- Thick vermilion border\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Van Maldergem syndrome"}],"image":"exported_images\/00106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Narrow chest\n- Thin ribs\n- Osteopenia\n- Motor delay\n- Neonatal hypotonia\n- Small for gestational age\n- Overlapping toe\n- Short columella\n- Hypoplasia of the corpus callosum\n- Highly arched eyebrow\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Microtia\n- Feeding difficulties\n- Flat face\n- Camptodactyly\n- Thick vermilion border\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Van Maldergem syndrome"}],"image":"exported_images\/00107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Narrow chest\n- Thin ribs\n- Osteopenia\n- Motor delay\n- Neonatal hypotonia\n- Small for gestational age\n- Overlapping toe\n- Short columella\n- Hypoplasia of the corpus callosum\n- Highly arched eyebrow\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Microtia\n- Feeding difficulties\n- Flat face\n- Camptodactyly\n- Thick vermilion border\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Van Maldergem syndrome"}],"image":"exported_images\/00108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA"}],"image":"exported_images\/00109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Delayed cranial suture closure\n- High forehead\n- Esotropia\n- Optic atrophy\n- Areflexia\n- Generalized hypotonia\n- Hepatosplenomegaly\n- Failure to thrive\n- Laryngomalacia\n- Weak cry\n- Hypertrophic cardiomyopathy\n- Dysphagia\n- Constipation\n- Dyspnea\n- Recurrent respiratory infections\n- Abdominal distention\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Feeding difficulties\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA"}],"image":"exported_images\/00110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Narrow forehead\n- Long philtrum\n- High forehead\n- Low-set ears\n- Prominent nasal bridge\n- Telecanthus\n- Esotropia\n- Blue sclerae\n- Carious teeth\n- Pectus carinatum\n- Hypotonia\n- Dysarthria\n- Atrial septal defect\n- Gait ataxia\n- Clumsiness\n- Cavum septum pellucidum\n- Scoliosis\n- Delayed skeletal maturation\n- Attention deficit hyperactivity disorder\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA"}],"image":"exported_images\/00111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Narrow forehead\n- Long philtrum\n- High forehead\n- Low-set ears\n- Prominent nasal bridge\n- Telecanthus\n- Esotropia\n- Blue sclerae\n- Carious teeth\n- Pectus carinatum\n- Hypotonia\n- Dysarthria\n- Gait ataxia\n- Clumsiness\n- Cavum septum pellucidum\n- Scoliosis\n- Delayed skeletal maturation\n- Attention deficit hyperactivity disorder\n- Severe global developmental delay\n- Feeding difficulties\n- Myoclonic seizure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA"}],"image":"exported_images\/00112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Long face\n- Deeply set eye\n- Delayed speech and language development\n- Motor delay\n- Frontal bossing\n- Gait ataxia\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Attention deficit hyperactivity disorder\n- Receptive language delay\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/00113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Long face\n- Deeply set eye\n- Delayed speech and language development\n- Motor delay\n- Frontal bossing\n- Gait ataxia\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Attention deficit hyperactivity disorder\n- Receptive language delay\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/00114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Long face\n- Deeply set eye\n- Cafe-au-lait spot\n- Global developmental delay\n- Motor delay\n- Polyhydramnios\n- Hypoglycemia\n- Frontal bossing\n- Gastroesophageal reflux\n- Gait ataxia\n- Generalized non-motor (absence) seizure\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Moderate receptive language delay\n- Esodeviation\n- Periventricular white matter hyperintensities\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/00115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Long face\n- Deeply set eye\n- Cafe-au-lait spot\n- Global developmental delay\n- Motor delay\n- Polyhydramnios\n- Hypoglycemia\n- Frontal bossing\n- Gastroesophageal reflux\n- Gait ataxia\n- Generalized non-motor (absence) seizure\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Moderate receptive language delay\n- Esodeviation\n- Periventricular white matter hyperintensities\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/00116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Ataxia\n- Global developmental delay\n- Neonatal hypotonia\n- Tremor\n- Intellectual disability, moderate\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Abnormal cerebral white matter morphology\n- Neonatal respiratory distress\n- Prolonged neonatal jaundice\n- Attention deficit hyperactivity disorder\n- Thick corpus callosum\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/00117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Facial hypotonia\n- Strabismus\n- Autism\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Gait ataxia\n- Intellectual disability, profound\n- Choroid plexus cyst\n- Unsteady gait\n- Decreased body weight\n- Thick corpus callosum\n- Focal-onset seizure\n- EEG with temporal sharp waves\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/00118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pursed lips\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Adducted thumb\n- Ulnar deviation of the hand or of fingers of the hand\n- Seizure\n- Motor delay\n- Talipes equinovarus\n- Short columella\n- Respiratory insufficiency\n- Scoliosis\n- Abnormal pattern of respiration\n- Elbow flexion contracture\n- Hip contracture\n- Prominent nasolabial fold\n- Knee flexion contracture\n- Enlarged naris\n- Chin with H-shaped crease\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; CLIFAHDD"}],"image":"exported_images\/00119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Pursed lips\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Esotropia\n- Delayed speech and language development\n- Nephrolithiasis\n- Adducted thumb\n- Ulnar deviation of the hand or of fingers of the hand\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Talipes equinovarus\n- Calcaneovalgus deformity\n- Short columella\n- Constipation\n- Gastroesophageal reflux\n- Cerebral atrophy\n- Respiratory insufficiency\n- Scoliosis\n- Abnormal pattern of respiration\n- Central apnea\n- Elbow flexion contracture\n- Hip contracture\n- Prominent nasolabial fold\n- Enlarged naris\n- Chin with H-shaped crease\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; CLIFAHDD"}],"image":"exported_images\/00120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Pursed lips\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Abnormal scapula morphology\n- 11 pairs of ribs\n- Adducted thumb\n- Ulnar deviation of the hand or of fingers of the hand\n- Hypotonia\n- Motor delay\n- Talipes equinovarus\n- Short columella\n- Respiratory insufficiency\n- Abnormal pattern of respiration\n- Elbow flexion contracture\n- Hip contracture\n- Prominent nasolabial fold\n- Knee flexion contracture\n- Enlarged naris\n- Chin with H-shaped crease\n- Camptodactyly\n- Abnormal pelvis bone morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; CLIFAHDD"}],"image":"exported_images\/00121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Mandibular prognathia\n- Hypertelorism\n- Narrow nasal bridge\n- Narrow nose\n- Shallow orbits\n- Long palpebral fissure\n- Osteopenia\n- Thin skin\n- Broad finger\n- Fine hair\n- Posterior fossa cyst\n- Sparse hair\n- Broad distal phalanx of finger\n- Sparse eyebrow\n- Lipoatrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PREMATURE AGING SYNDROME, PENTTINEN TYPE; PENTT"}],"image":"exported_images\/00122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Short stature\n- Maxillozygomatic hypoplasia\n- Anotia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN"}],"image":"exported_images\/00123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Malar flattening\n- Micrognathia\n- Abnormal pinna morphology\n- Downslanted palpebral fissures\n- Brachydactyly\n- Broad finger\n- Microtia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN"}],"image":"exported_images\/00124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Everted lower lip vermilion\n- Abnormality of the orbital region\n- Micrognathia\n- Hearing impairment\n- Cupped ear\n- Sparse eyelashes\n- Delayed eruption of primary teeth\n- Alopecia\n- Short nose\n- Abnormal zygomatic arch morphology\n- Persistence of primary teeth\n- Microtia\n- Abnormality of the temporomandibular joint\n- Ablepharon\n- White hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA"}],"image":"exported_images\/00125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glossoptosis\n- Cleft palate\n- Trismus\n- Everted lower lip vermilion\n- Abnormality of the orbital region\n- Micrognathia\n- Hearing impairment\n- Stenosis of the external auditory canal\n- Sparse eyelashes\n- Dental crowding\n- Alopecia\n- Bicuspid aortic valve\n- Upper airway obstruction\n- Short nose\n- Postauricular pit\n- Abnormal zygomatic arch morphology\n- Microtia\n- Abnormality of the temporomandibular joint\n- Aplasia\/Hypoplasia of the eyelid\n- Temporomandibular joint ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA"}],"image":"exported_images\/00126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the orbital region\n- Hearing impairment\n- Preauricular skin tag\n- Lower eyelid coloboma\n- Alopecia\n- Short nose\n- Preauricular pit\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA"}],"image":"exported_images\/00127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anteverted nares\n- Strabismus\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Narrow chest\n- Joint laxity\n- Intellectual disability, moderate\n- Polyphagia\n- 2-3 toe syndactyly\n- Infantile muscular hypotonia\n- Posterior plagiocephaly\n- Wide nasal base\n- Frequent temper tantrums\n- Displaced tracheal bronchus\n- Schizophrenia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anteverted nares\n- Strabismus\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Narrow chest\n- Joint laxity\n- Intellectual disability, moderate\n- Polyphagia\n- 2-3 toe syndactyly\n- Infantile muscular hypotonia\n- Posterior plagiocephaly\n- Wide nasal base\n- Frequent temper tantrums\n- Displaced tracheal bronchus\n- Schizophrenia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anteverted nares\n- Strabismus\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Narrow chest\n- Joint laxity\n- Intellectual disability, moderate\n- Polyphagia\n- 2-3 toe syndactyly\n- Infantile muscular hypotonia\n- Posterior plagiocephaly\n- Wide nasal base\n- Frequent temper tantrums\n- Displaced tracheal bronchus\n- Schizophrenia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anteverted nares\n- Strabismus\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Narrow chest\n- Joint laxity\n- Intellectual disability, moderate\n- Polyphagia\n- 2-3 toe syndactyly\n- Infantile muscular hypotonia\n- Posterior plagiocephaly\n- Wide nasal base\n- Frequent temper tantrums\n- Displaced tracheal bronchus\n- Schizophrenia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Broad forehead\n- Narrow forehead\n- Strabismus\n- Blue irides\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Intellectual disability, moderate\n- Short 5th finger\n- Prominent forehead\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Narrow mouth\n- Hypertelorism\n- Prominent supraorbital ridges\n- Downslanted palpebral fissures\n- Proptosis\n- Tooth malposition\n- Brachydactyly\n- Short nail\n- Nail dysplasia\n- Absent frontal sinuses\n- Femoral bowing\n- Elbow flexion contracture\n- Dislocated radial head\n- Short nose\n- Irregular iliac crest\n- Short stature\n- Decreased body weight\n- Hyperostosis frontalis interna\n- Bilateral conductive hearing impairment\n- Median cleft palate\n- Broad distal phalanx of the thumb\n- Short distal phalanx of the thumb\n- Broad hallux\n- Broad distal phalanx of the hallux\n- Short distal phalanx of hallux\n- Short hallux\n- Prominent forehead\n- Broad thumb\n- Abnormal nasal base norphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE II; OPD2"}],"image":"exported_images\/00133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DONNAI-BARROW SYNDROME"}],"image":"exported_images\/00134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Hearing impairment\n- Downslanted palpebral fissures\n- Cataract\n- Myopia\n- Chorioretinal coloboma\n- Iris coloboma\n- Global developmental delay\n- Agenesis of corpus callosum\n- Omphalocele\n- Intestinal malrotation\n- Chiari type I malformation\n- Frontal encephalocele\n- Slow decrease in visual acuity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DONNAI-BARROW SYNDROME"}],"image":"exported_images\/00135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAJDU-CHENEY SYNDROME; HJCYS"}],"image":"exported_images\/00136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAJDU-CHENEY SYNDROME; HJCYS"}],"image":"exported_images\/00137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Urofacial syndrome"}],"image":"exported_images\/00138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Urofacial syndrome"}],"image":"exported_images\/00139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAJDU-CHENEY SYNDROME; HJCYS"}],"image":"exported_images\/00140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ectodermal dysplasia (select examples)"}],"image":"exported_images\/00141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"APERT SYNDROME"}],"image":"exported_images\/00142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DONNAI-BARROW SYNDROME"}],"image":"exported_images\/00143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/00145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ectodermal dysplasia (select examples)"}],"image":"exported_images\/00146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME B; CSB"}],"image":"exported_images\/00147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Focal facial dermal dysplasia"}],"image":"exported_images\/00149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA"}],"image":"exported_images\/00150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA"}],"image":"exported_images\/00151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA"}],"image":"exported_images\/00152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR; DEDSSH"}],"image":"exported_images\/00153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR; DEDSSH"}],"image":"exported_images\/00154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR; DEDSSH"}],"image":"exported_images\/00155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR; DEDSSH"}],"image":"exported_images\/00156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY; SINO"}],"image":"exported_images\/00157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF"}],"image":"exported_images\/00166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF"}],"image":"exported_images\/00167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF"}],"image":"exported_images\/00168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL"}],"image":"exported_images\/00169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL"}],"image":"exported_images\/00170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL"}],"image":"exported_images\/00171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL"}],"image":"exported_images\/00172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL"}],"image":"exported_images\/00173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL\/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME; FHEIG"}],"image":"exported_images\/00174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL\/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME; FHEIG"}],"image":"exported_images\/00175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL\/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME; FHEIG"}],"image":"exported_images\/00176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL\/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME; FHEIG"}],"image":"exported_images\/00177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34; MRXS34"}],"image":"exported_images\/00178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34; MRXS34"}],"image":"exported_images\/00179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION; NEDCPMD"}],"image":"exported_images\/00180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION; NEDCPMD"}],"image":"exported_images\/00181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"APERT SYNDROME"}],"image":"exported_images\/00182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kenny-Caffey syndrome"}],"image":"exported_images\/00183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"APERT SYNDROME"}],"image":"exported_images\/00184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Acrodysostosis"}],"image":"exported_images\/00185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Narrow chest\n- Intellectual disability\n- Dysarthria\n- Distal muscle weakness\n- Equinovarus deformity\n- Ulnar deviation of finger\n- Radial deviation of finger\n- Proximal placement of thumb\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis multiplex congenita"}],"image":"exported_images\/00186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ABLEPHARON-MACROSTOMIA SYNDROME; AMS"}],"image":"exported_images\/00187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEIPERT SYNDROME; KPTS"}],"image":"exported_images\/00188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEIPERT SYNDROME; KPTS"}],"image":"exported_images\/00189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEIPERT SYNDROME; KPTS"}],"image":"exported_images\/00190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEIPERT SYNDROME; KPTS"}],"image":"exported_images\/00191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEIPERT SYNDROME; KPTS"}],"image":"exported_images\/00192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CSNK1G1"}],"image":"exported_images\/00193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CSNK1G1"}],"image":"exported_images\/00194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CSNK1G1"}],"image":"exported_images\/00195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Blepharophimosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, X-LINKED; OHDOX"}],"image":"exported_images\/00196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, X-LINKED; OHDOX"}],"image":"exported_images\/00197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, X-LINKED; OHDOX"}],"image":"exported_images\/00198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUENKE SYNDROME; MNKES"}],"image":"exported_images\/00199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dilatation of the renal pelvis\n- Bladder trabeculation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Urofacial syndrome"}],"image":"exported_images\/00200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Polycystic kidney dysplasia\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Posteriorly rotated ears\n- Abnormal pinna morphology\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Hypotelorism\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Foot acroosteolysis\n- Wormian bones\n- Downturned corners of mouth\n- Abnormal vertebral morphology\n- Abnormal cervical curvature\n- Basilar invagination\n- Serpentine fibula\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAJDU-CHENEY SYNDROME; HJCYS"}],"image":"exported_images\/00201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Epicanthus\n- Bulbous nose\n- Subcapsular cataract\n- Myopia\n- Esotropia\n- Joint hypermobility\n- Posterior vitreous detachment\n- Pes planus\n- Highly arched eyebrow\n- Genu recurvatum\n- Abnormal vitreous humor morphology\n- Macular atrophy\n- Abnormality of circulating beta-2-microglobulin level\n- Knee pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DONNAI-BARROW SYNDROME"}],"image":"exported_images\/00202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Velopharyngeal insufficiency\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Narrow nose\n- Blepharophimosis\n- Hypoparathyroidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VELOCARDIOFACIAL SYNDROME; VCFS"}],"image":"exported_images\/00203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Cleft palate\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Mixed hearing impairment\n- Downslanted palpebral fissures\n- Ptosis\n- Hypotonia\n- Global developmental delay\n- Joint hypermobility\n- High pitched voice\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Coarse hair\n- Scoliosis\n- Vertebral fusion\n- Short stature\n- Ascending tubular aorta aneurysm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Cleft palate\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Mixed hearing impairment\n- Downslanted palpebral fissures\n- Ptosis\n- Hypotonia\n- Global developmental delay\n- Joint hypermobility\n- High pitched voice\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Coarse hair\n- Scoliosis\n- Vertebral fusion\n- Short stature\n- Ascending tubular aorta aneurysm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Epicanthus\n- Facial hypotonia\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Dental crowding\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Joint hypermobility\n- Bell-shaped thorax\n- High pitched voice\n- Tethered cord\n- Woolly hair\n- Meningocele\n- Low back pain\n- Short stature\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Epicanthus\n- Facial hypotonia\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Dental crowding\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Joint hypermobility\n- Bell-shaped thorax\n- High pitched voice\n- Tethered cord\n- Woolly hair\n- Meningocele\n- Low back pain\n- Short stature\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Epicanthus\n- Facial hypotonia\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Dental crowding\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Joint hypermobility\n- Bell-shaped thorax\n- High pitched voice\n- Tethered cord\n- Woolly hair\n- Meningocele\n- Low back pain\n- Short stature\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Nystagmus\n- Carious teeth\n- Conical tooth\n- Cutis laxa\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Thoracic kyphosis\n- Progressive flexion contractures\n- Enamel hypoplasia\n- Corneal opacity\n- Bilateral conductive hearing impairment\n- Progressive loss of facial adipose tissue\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME B; CSB"}],"image":"exported_images\/00209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Round face\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Laryngomalacia\n- Sparse scalp hair\n- CNS hypomyelination\n- Prominent metopic ridge\n- Prolonged neonatal jaundice\n- High anterior hairline\n- Intellectual disability, severe\n- Gastrostomy tube feeding in infancy\n- Maintenance insomnia\n- Terminal insomnia\n- Limb tremor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES; NEDHYMS"}],"image":"exported_images\/00210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Thick lower lip vermilion\n- Gingival overgrowth\n- Anteverted nares\n- Deeply set eye\n- Developmental cataract\n- Thick eyebrow\n- Reduced eye contact\n- Dry skin\n- Hypohidrosis\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Reduced tendon reflexes\n- Absent speech\n- Failure to thrive\n- Gray matter heterotopia\n- Poor head control\n- Short nasal bridge\n- Foot dorsiflexor weakness\n- Protruding tongue\n- Gastrostomy tube feeding in infancy\n- Infantile spasms\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION; NEDHRIT"}],"image":"exported_images\/00211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low anterior hairline\n- Thick eyebrow\n- Hypotonia\n- Spasticity\n- Reduced tendon reflexes\n- Recurrent fever\n- Hepatomegaly\n- Global brain atrophy\n- Poor head control\n- Neonatal respiratory distress\n- Feeding difficulties\n- Nasogastric tube feeding\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION; NEDHRIT"}],"image":"exported_images\/00212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Gingival overgrowth\n- Retrognathia\n- Low-set ears\n- Hypotonia\n- Spasticity\n- Hyperreflexia\n- Premature birth\n- Mitral regurgitation\n- Gastroesophageal reflux\n- Apnea\n- Poor head control\n- Neonatal respiratory distress\n- Tracheomalacia\n- Tricuspid regurgitation\n- Depressed nasal bridge\n- Stridor\n- Horizontal eyebrow\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Infantile spasms\n- Thick vermilion border\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION; NEDHRIT"}],"image":"exported_images\/00213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABAIS SA-DE VRIES SYNDROME, TYPE 1; NSDVS1"}],"image":"exported_images\/00214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS2"}],"image":"exported_images\/00215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS2"}],"image":"exported_images\/00216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS2"}],"image":"exported_images\/00217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH"}],"image":"exported_images\/00218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76; DEE76"}],"image":"exported_images\/00219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76; DEE76"}],"image":"exported_images\/00220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76; DEE76"}],"image":"exported_images\/00221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76; DEE76"}],"image":"exported_images\/00222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCAF4"}],"image":"exported_images\/00223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCAF4"}],"image":"exported_images\/00224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCAF4"}],"image":"exported_images\/00225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCAF4"}],"image":"exported_images\/00226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS"}],"image":"exported_images\/00227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS"}],"image":"exported_images\/00228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS"}],"image":"exported_images\/00229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS"}],"image":"exported_images\/00230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LI-CAMPEAU SYNDROME; LICAS"}],"image":"exported_images\/00231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LI-CAMPEAU SYNDROME; LICAS"}],"image":"exported_images\/00232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LI-CAMPEAU SYNDROME; LICAS"}],"image":"exported_images\/00233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LI-CAMPEAU SYNDROME; LICAS"}],"image":"exported_images\/00234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG"}],"image":"exported_images\/00235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG"}],"image":"exported_images\/00236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/00237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHANARIN-DORFMAN SYNDROME; CDS"}],"image":"exported_images\/00238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHANARIN-DORFMAN SYNDROME; CDS"}],"image":"exported_images\/00239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHANARIN-DORFMAN SYNDROME; CDS"}],"image":"exported_images\/00240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Horseshoe kidney\n- Ectopic kidney\n- Narrow mouth\n- High palate\n- Brachycephaly\n- Wide anterior fontanel\n- Abnormality of the face\n- Abnormal mandible morphology\n- Microretrognathia\n- Hypertelorism\n- Smooth philtrum\n- Short philtrum\n- Narrow forehead\n- Abnormality of the outer ear\n- Bulbous nose\n- Abnormality of the eye\n- Strabismus\n- Myopia\n- Delayed speech and language development\n- Short sternum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Growth delay\n- Frontal bossing\n- Abnormality of the lower limb\n- Birth length less than 3rd percentile\n- Abnormal nipple morphology\n- 2-3 toe cutaneous syndactyly\n- Low hanging columella\n- Triangular shaped phalanges of the hand\n- Absent cupid's bow\n- Prominent forehead\n- Primary microcephaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Horseshoe kidney\n- Ectopic kidney\n- Narrow mouth\n- High palate\n- Brachycephaly\n- Wide anterior fontanel\n- Abnormality of the face\n- Abnormal mandible morphology\n- Microretrognathia\n- Hypertelorism\n- Smooth philtrum\n- Short philtrum\n- Narrow forehead\n- Abnormality of the outer ear\n- Bulbous nose\n- Abnormality of the eye\n- Strabismus\n- Myopia\n- Delayed speech and language development\n- Short sternum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Growth delay\n- Frontal bossing\n- Abnormality of the lower limb\n- Birth length less than 3rd percentile\n- Abnormal nipple morphology\n- 2-3 toe cutaneous syndactyly\n- Low hanging columella\n- Triangular shaped phalanges of the hand\n- Absent cupid's bow\n- Prominent forehead\n- Primary microcephaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Horseshoe kidney\n- Ectopic kidney\n- Narrow mouth\n- High palate\n- Brachycephaly\n- Wide anterior fontanel\n- Abnormality of the face\n- Abnormal mandible morphology\n- Microretrognathia\n- Hypertelorism\n- Smooth philtrum\n- Short philtrum\n- Narrow forehead\n- Abnormality of the outer ear\n- Bulbous nose\n- Abnormality of the eye\n- Strabismus\n- Myopia\n- Delayed speech and language development\n- Short sternum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Growth delay\n- Frontal bossing\n- Abnormality of the lower limb\n- Birth length less than 3rd percentile\n- Abnormal nipple morphology\n- 2-3 toe cutaneous syndactyly\n- Low hanging columella\n- Triangular shaped phalanges of the hand\n- Absent cupid's bow\n- Prominent forehead\n- Primary microcephaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Horseshoe kidney\n- Ectopic kidney\n- Narrow mouth\n- High palate\n- Brachycephaly\n- Wide anterior fontanel\n- Abnormality of the face\n- Abnormal mandible morphology\n- Microretrognathia\n- Hypertelorism\n- Smooth philtrum\n- Short philtrum\n- Narrow forehead\n- Abnormality of the outer ear\n- Bulbous nose\n- Abnormality of the eye\n- Strabismus\n- Myopia\n- Delayed speech and language development\n- Short sternum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Growth delay\n- Frontal bossing\n- Abnormality of the lower limb\n- Birth length less than 3rd percentile\n- Abnormal nipple morphology\n- 2-3 toe cutaneous syndactyly\n- Low hanging columella\n- Triangular shaped phalanges of the hand\n- Absent cupid's bow\n- Prominent forehead\n- Primary microcephaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Abnormality of the face\n- Abnormal mandible morphology\n- Retrognathia\n- Short philtrum\n- Abnormality of the eye\n- Myopia\n- Atypical behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sacral dimple\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Tremor\n- Growth delay\n- Constipation\n- Abnormality of the lower limb\n- Birth length less than 3rd percentile\n- Aplasia cutis congenita over the scalp vertex\n- 2-3 toe cutaneous syndactyly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of eye movement\n- Ptosis\n- Hyporeflexia\n- Cardiomyopathy\n- Pes cavus\n- Achilles tendon contracture\n- Inability to walk\n- Respiratory insufficiency due to muscle weakness\n- Myopathy\n- Neck flexor weakness\n- Type 1 fibers relatively smaller than type 2 fibers\n- Respiratory failure requiring assisted ventilation\n- Flexion contracture of finger\n- Weakness of facial musculature\n- Jaw contracture\n- Increased endomysial connective tissue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myopathy, centronuclear"}],"image":"exported_images\/00246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ptosis\n- Hyporeflexia\n- Achilles tendon contracture\n- Poor head control\n- Scoliosis\n- Respiratory insufficiency due to muscle weakness\n- Myopathy\n- Neck flexor weakness\n- Type 1 fibers relatively smaller than type 2 fibers\n- Respiratory failure requiring assisted ventilation\n- Feeding difficulties in infancy\n- Weakness of facial musculature\n- Increased endomysial connective tissue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myopathy, centronuclear"}],"image":"exported_images\/00247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of eye movement\n- Ptosis\n- Hyporeflexia\n- Achilles tendon contracture\n- Poor head control\n- Inability to walk\n- Scoliosis\n- Respiratory insufficiency due to muscle weakness\n- Elbow flexion contracture\n- Muscular dystrophy\n- Neck flexor weakness\n- Respiratory failure requiring assisted ventilation\n- Congenital finger flexion contractures\n- Feeding difficulties in infancy\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myopathy, centronuclear"}],"image":"exported_images\/00248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormality of eye movement\n- Ptosis\n- Hyporeflexia\n- Achilles tendon contracture\n- Poor head control\n- Scoliosis\n- Respiratory insufficiency due to muscle weakness\n- Myopathy\n- Muscular dystrophy\n- Neck flexor weakness\n- Type 1 fibers relatively smaller than type 2 fibers\n- Mildly elevated creatine kinase\n- Feeding difficulties in infancy\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myopathy, centronuclear"}],"image":"exported_images\/00249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Bifid uvula\n- High palate\n- Velopharyngeal insufficiency\n- Malar flattening\n- Low-set ears\n- Webbed neck\n- Delayed speech and language development\n- Hypertrophic cardiomyopathy\n- Cardiomegaly\n- Pes planus\n- Achilles tendon contracture\n- Clinodactyly of the 5th toe\n- Low posterior hairline\n- Thoracolumbar scoliosis\n- Fused cervical vertebrae\n- Elbow flexion contracture\n- Syringomyelia\n- Lunate-triquetral fusion\n- Short stature\n- Absent patellar reflexes\n- Chiari type I malformation\n- Thoracic hemivertebrae\n- Attached earlobe\n- Clinodactyly of the 4th toe\n- Systolic heart murmur\n- Clinodactyly of the 2nd finger\n- Small hand\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiomyopathy, familial hypertrophic"}],"image":"exported_images\/00250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bifid uvula\n- Velopharyngeal insufficiency\n- Retrognathia\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Wide nose\n- Webbed neck\n- Broad neck\n- Upslanted palpebral fissure\n- Global developmental delay\n- Generalized hypotonia\n- Failure to thrive\n- Ascites\n- Atrial septal defect\n- Hypertrophic cardiomyopathy\n- Right-to-left shunt\n- Abnormal left ventricle morphology\n- Left ventricular hypertrophy\n- Short distal phalanx of toe\n- Abnormal cortical gyration\n- Distal arthrogryposis\n- Absent proximal finger flexion creases\n- Wide intermamillary distance\n- Focal white matter lesions\n- Shoulder muscle hypoplasia\n- Short thumb\n- Short distal phalanx of finger\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiomyopathy, familial hypertrophic"}],"image":"exported_images\/00251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Growth abnormality\n- Overgrowth\n- Abnormal facial shape\n- Delayed gross motor development\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53; MRD53"}],"image":"exported_images\/00252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Growth abnormality\n- Abnormal facial shape\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53; MRD53"}],"image":"exported_images\/00253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Intellectual disability, mild\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- EEG abnormality\n- Abnormality of the digestive system\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- EEG abnormality\n- Abnormality of the digestive system\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Growth abnormality\n- Abnormal facial shape\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Growth abnormality\n- Abnormal facial shape\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Growth abnormality\n- Abnormal facial shape\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/00265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary retention\n- Abnormality of male external genitalia\n- Micropenis\n- Abnormality of the ureter\n- Abnormality of the kidney\n- Abnormality of the outer ear\n- Hearing impairment\n- Low-set ears\n- Abnormality of the eye\n- Abnormal optic nerve morphology\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Sacral dimple\n- Intellectual disability\n- Seizure\n- Motor delay\n- Abnormality of the cardiovascular system\n- Patent ductus arteriosus\n- Tracheomalacia\n- Abnormality of the upper limb\n- Birth length less than 3rd percentile\n- Laryngeal cleft\n- Aplasia\/Hypoplasia of the thumb\n- Fetal pyelectasis\n- Feeding difficulties\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/00267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Intellectual disability\n- Spasticity\n- Motor delay\n- Achilles tendon contracture\n- Apnea\n- Bilateral camptodactyly\n- Equinovarus deformity\n- Small toe\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis multiplex congenita"}],"image":"exported_images\/00268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Wide mouth\n- Macroglossia\n- High palate\n- Brachycephaly\n- Microcephaly\n- Coarse facial features\n- Hypertelorism\n- Narrow forehead\n- Otitis media\n- Ptosis\n- Long eyelashes\n- Abnormality of the ear\n- Ectropion\n- Narrow chest\n- Pruritus\n- Hypotonia\n- Reduced tendon reflexes\n- Plagiocephaly\n- Hip dysplasia\n- Joint laxity\n- Decreased fetal movement\n- Abnormal hair morphology\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Bradycardia\n- Abnormal cardiac ventricle morphology\n- Short foot\n- Bilateral talipes equinovarus\n- Overlapping toe\n- Chronic diarrhea\n- Cerebral atrophy\n- Hypoplastic nipples\n- Steatorrhea\n- Downturned corners of mouth\n- Recurrent infections\n- Immunodeficiency\n- Rickets\n- Hip dislocation\n- Obstructive sleep apnea\n- Absent Achilles reflex\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Abnormality of bone mineral density\n- Abnormal nasal morphology\n- Distal arthrogryposis\n- Almond-shaped palpebral fissure\n- Fibular bowing\n- Severe global developmental delay\n- Midface retrusion\n- Thoracic hypertrichosis\n- Abnormal renal morphology\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS"}],"image":"exported_images\/00269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Abnormality of the dentition\n- High palate\n- Brachycephaly\n- Microcephaly\n- Coarse facial features\n- Epicanthus\n- Hypertelorism\n- Narrow forehead\n- Abnormality of the nose\n- Otitis media\n- Ptosis\n- Abnormality of the ear\n- Synophrys\n- Atypical behavior\n- Hypothyroidism\n- Pruritus\n- Seizure\n- Hypotonia\n- Hyperreflexia\n- Plagiocephaly\n- Joint laxity\n- Hepatosplenomegaly\n- Small for gestational age\n- Decreased fetal movement\n- Abnormal hair morphology\n- Short foot\n- Overlapping toe\n- Gastroesophageal reflux\n- Cerebral atrophy\n- Respiratory distress\n- EEG abnormality\n- Hypoplastic nipples\n- Scoliosis\n- Downturned corners of mouth\n- Recurrent infections\n- Immunodeficiency\n- Rickets\n- Genu valgum\n- Obstructive sleep apnea\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Distal arthrogryposis\n- Nail dystrophy\n- Central sleep apnea\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Midface retrusion\n- Thoracic hypertrichosis\n- Increased serum bile acid concentration\n- Thick vermilion border\n- Cerebral visual impairment\n- Abnormal liver morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS"}],"image":"exported_images\/00270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Abnormality of the dentition\n- High palate\n- Brachycephaly\n- Microcephaly\n- Narrow forehead\n- Abnormality of the nose\n- Otitis media\n- Ptosis\n- Hypermetropia\n- Abnormality of the ear\n- Synophrys\n- Atypical behavior\n- Pectus excavatum\n- Pruritus\n- Cholelithiasis\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Cerebellar hypoplasia\n- Hyperreflexia\n- Hip dysplasia\n- Joint laxity\n- Decreased liver function\n- Abnormal hair morphology\n- Bradycardia\n- Short foot\n- Bilateral talipes equinovarus\n- Overlapping toe\n- Gastroesophageal reflux\n- Chronic diarrhea\n- Cerebral atrophy\n- Respiratory distress\n- Abnormal cerebral ventricle morphology\n- Coarse hair\n- EEG abnormality\n- Abnormal cerebral white matter morphology\n- Hypoplastic nipples\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Distal arthrogryposis\n- Bilateral coxa valga\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Thoracic hypertrichosis\n- Increased serum bile acid concentration\n- Thick vermilion border\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS"}],"image":"exported_images\/00271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Abnormality of the dentition\n- High palate\n- Brachycephaly\n- Microcephaly\n- Narrow forehead\n- Abnormality of the nose\n- Otitis media\n- Ptosis\n- Hypermetropia\n- Abnormality of the ear\n- Synophrys\n- Atypical behavior\n- Pectus excavatum\n- Pruritus\n- Cholelithiasis\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Cerebellar hypoplasia\n- Hyperreflexia\n- Hip dysplasia\n- Joint laxity\n- Decreased liver function\n- Abnormal hair morphology\n- Bradycardia\n- Short foot\n- Bilateral talipes equinovarus\n- Overlapping toe\n- Gastroesophageal reflux\n- Chronic diarrhea\n- Cerebral atrophy\n- Respiratory distress\n- Abnormal cerebral ventricle morphology\n- Coarse hair\n- EEG abnormality\n- Abnormal cerebral white matter morphology\n- Hypoplastic nipples\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Distal arthrogryposis\n- Bilateral coxa valga\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Thoracic hypertrichosis\n- Increased serum bile acid concentration\n- Thick vermilion border\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS"}],"image":"exported_images\/00272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIZON-ISIDOR SYNDROME; NIZIDS"}],"image":"exported_images\/00278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIZON-ISIDOR SYNDROME; NIZIDS"}],"image":"exported_images\/00279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES; NEDBAVC"}],"image":"exported_images\/00280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES; NEDBAVC"}],"image":"exported_images\/00281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MCCUNE-ALBRIGHT SYNDROME; MAS"}],"image":"exported_images\/00282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Global developmental delay\n- Intrauterine growth retardation\n- Oligohydramnios\n- Intestinal malrotation\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIN3B"}],"image":"exported_images\/00283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34; MRXS34"}],"image":"exported_images\/00284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34; MRXS34"}],"image":"exported_images\/00285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Dolichocephaly\n- Retrognathia\n- Short philtrum\n- Narrow forehead\n- Micrognathia\n- Tapered finger\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Oligohydramnios\n- Frontal upsweep of hair\n- Medial flaring of the eyebrow\n- Tented upper lip vermilion\n- Bridged palmar crease\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Dolichocephaly\n- Retrognathia\n- Short philtrum\n- Narrow forehead\n- Micrognathia\n- Tapered finger\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Oligohydramnios\n- Frontal upsweep of hair\n- Medial flaring of the eyebrow\n- Tented upper lip vermilion\n- Bridged palmar crease\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Dolichocephaly\n- Retrognathia\n- Short philtrum\n- Narrow forehead\n- Micrognathia\n- Tapered finger\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Oligohydramnios\n- Frontal upsweep of hair\n- Medial flaring of the eyebrow\n- Tented upper lip vermilion\n- Bridged palmar crease\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Cleft soft palate\n- Broad alveolar ridges\n- Open mouth\n- Thin upper lip vermilion\n- Retrognathia\n- Micrognathia\n- Sacral dimple\n- Global developmental delay\n- Generalized hypotonia\n- Muscle weakness\n- Patent foramen ovale\n- Phimosis\n- Pes cavus\n- Short foot\n- Clonus\n- Downturned corners of mouth\n- Easy fatigability\n- Feeding difficulties in infancy\n- Short thumb\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/00292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Amblyopia\n- Autism\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Hirsutism\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- Broad-based gait\n- Cortical dysplasia\n- Peripheral retinal avascularization\n- Subependymal nodules\n- Nummular eczema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/00293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Dental crowding\n- Prominent superficial veins\n- Intention tremor\n- Wormian bones\n- Lipoatrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARBACH-RUSTAD PROGEROID SYNDROME; MARUPS"}],"image":"exported_images\/00294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67"}],"image":"exported_images\/00295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67"}],"image":"exported_images\/00296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67"}],"image":"exported_images\/00297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67"}],"image":"exported_images\/00298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67"}],"image":"exported_images\/00299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 26; SCA26"}],"image":"exported_images\/00300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/00308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS; NFSRA"}],"image":"exported_images\/00309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS; NFSRA"}],"image":"exported_images\/00310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/00318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND\/OR STRUCTURAL BRAIN ABNORMALITIES; NEDASB"}],"image":"exported_images\/00319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND\/OR STRUCTURAL BRAIN ABNORMALITIES; NEDASB"}],"image":"exported_images\/00320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS"}],"image":"exported_images\/00321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE; SDJLABA"}],"image":"exported_images\/00322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY; NEDESBA"}],"image":"exported_images\/00323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY; NEDESBA"}],"image":"exported_images\/00324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY; NEDESBA"}],"image":"exported_images\/00325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY; NEDESBA"}],"image":"exported_images\/00326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY; NEDESBA"}],"image":"exported_images\/00327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY; NEDBASS"}],"image":"exported_images\/00328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY; NEDBASS"}],"image":"exported_images\/00329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY; NEDBASS"}],"image":"exported_images\/00330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES; PAMDDFS"}],"image":"exported_images\/00331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES; PAMDDFS"}],"image":"exported_images\/00332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES; PAMDDFS"}],"image":"exported_images\/00333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES; NEDMABA"}],"image":"exported_images\/00334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES; NEDMABA"}],"image":"exported_images\/00335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES; NEDMABA"}],"image":"exported_images\/00336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES; NEDMABA"}],"image":"exported_images\/00337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES; NEDBAS"}],"image":"exported_images\/00338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES; NEDBAS"}],"image":"exported_images\/00339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED"}],"image":"exported_images\/00340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED"}],"image":"exported_images\/00341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED"}],"image":"exported_images\/00342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED"}],"image":"exported_images\/00343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM"}],"image":"exported_images\/00344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM"}],"image":"exported_images\/00345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM"}],"image":"exported_images\/00346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM"}],"image":"exported_images\/00347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE; SEMDSP"}],"image":"exported_images\/00348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE; SEMDSP"}],"image":"exported_images\/00349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT; NEDSSWI"}],"image":"exported_images\/00350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT; NEDSSWI"}],"image":"exported_images\/00351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Dental crowding\n- Prominent superficial veins\n- Intention tremor\n- Wormian bones\n- Lipoatrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARBACH-RUSTAD PROGEROID SYNDROME; MARUPS"}],"image":"exported_images\/00352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichothiodystrophy"}],"image":"exported_images\/00353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CULLER-JONES SYNDROME; CJS"}],"image":"exported_images\/00354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CULLER-JONES SYNDROME; CJS"}],"image":"exported_images\/00355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES; NDCAGF"}],"image":"exported_images\/00356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY; SOFM"}],"image":"exported_images\/00364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY; SOFM"}],"image":"exported_images\/00365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 5; MRT5"}],"image":"exported_images\/00366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND"}],"image":"exported_images\/00367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND"}],"image":"exported_images\/00368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18; DEE18"}],"image":"exported_images\/00369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS; ABS1"}],"image":"exported_images\/00370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CATEL-MANZKE SYNDROME; CATMANS"}],"image":"exported_images\/00371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CATEL-MANZKE SYNDROME; CATMANS"}],"image":"exported_images\/00372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES; SIMHA"}],"image":"exported_images\/00373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES; SIMHA"}],"image":"exported_images\/00374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES; SIMHA"}],"image":"exported_images\/00375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES; SIMHA"}],"image":"exported_images\/00376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1"}],"image":"exported_images\/00377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STEEL SYNDROME; STLS"}],"image":"exported_images\/00378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STEEL SYNDROME; STLS"}],"image":"exported_images\/00379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS; FDLAB"}],"image":"exported_images\/00380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAM20B"}],"image":"exported_images\/00382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAM20B"}],"image":"exported_images\/00383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Triangular face\n- Low-set ears\n- Broad nasal tip\n- Deeply set eye\n- Myopia\n- Ventriculomegaly\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PAGANINI-MIOZZO SYNDROME; MRXSPM"}],"image":"exported_images\/00384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES; NEDMIBA"}],"image":"exported_images\/00385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES; NEDMIBA"}],"image":"exported_images\/00386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULOSKELETODENTAL SYNDROME; OCSKD"}],"image":"exported_images\/00387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULOSKELETODENTAL SYNDROME; OCSKD"}],"image":"exported_images\/00388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 39; MRT39"}],"image":"exported_images\/00389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY; GDRM"}],"image":"exported_images\/00390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY; GDRM"}],"image":"exported_images\/00391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY; GDRM"}],"image":"exported_images\/00392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SEIZURES, SCOLIOSIS, AND MACROCEPHALY\/MICROCEPHALY SYNDROME; SSMS"}],"image":"exported_images\/00393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/00394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/00395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN-GIBSON SYNDROME; COGIS"}],"image":"exported_images\/00396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN-GIBSON SYNDROME; COGIS"}],"image":"exported_images\/00397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN-GIBSON SYNDROME; COGIS"}],"image":"exported_images\/00398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/00399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/00400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/00401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/00402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS; IDDSFAS"}],"image":"exported_images\/00403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS; IDDSFAS"}],"image":"exported_images\/00404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS; IDDSFAS"}],"image":"exported_images\/00405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS; IDDSFAS"}],"image":"exported_images\/00406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YWHAZ"}],"image":"exported_images\/00407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YWHAZ"}],"image":"exported_images\/00408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YWHAZ"}],"image":"exported_images\/00409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YWHAZ"}],"image":"exported_images\/00410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAUNDES-BANKA SYNDROME; FABAS"}],"image":"exported_images\/00415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAUNDES-BANKA SYNDROME; FABAS"}],"image":"exported_images\/00416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAUNDES-BANKA SYNDROME; FABAS"}],"image":"exported_images\/00417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAUNDES-BANKA SYNDROME; FABAS"}],"image":"exported_images\/00418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19"}],"image":"exported_images\/00419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19"}],"image":"exported_images\/00420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SULEIMAN-EL-HATTAB SYNDROME; SULEHS"}],"image":"exported_images\/00421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SULEIMAN-EL-HATTAB SYNDROME; SULEHS"}],"image":"exported_images\/00422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Desbuquois dysplasia"}],"image":"exported_images\/00423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Thickened helices\n- Nystagmus\n- Brachydactyly\n- Seizure\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Deep philtrum\n- Highly arched eyebrow\n- Clinodactyly of the 5th finger\n- Short 4th metacarpal\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95; DEE95"}],"image":"exported_images\/00424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95; DEE95"}],"image":"exported_images\/00425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95; DEE95"}],"image":"exported_images\/00426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB-SHAFFER SYNDROME; LAMSHF"}],"image":"exported_images\/00427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GABRIELE-DE VRIES SYNDROME; GADEVS"}],"image":"exported_images\/00428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 98; XLID98"}],"image":"exported_images\/00429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIX2"}],"image":"exported_images\/00430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIX2"}],"image":"exported_images\/00431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIX2"}],"image":"exported_images\/00432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR"}],"image":"exported_images\/00433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR"}],"image":"exported_images\/00434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR"}],"image":"exported_images\/00435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Otofaciocervical syndrome"}],"image":"exported_images\/00436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME; AAMR"}],"image":"exported_images\/00437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47"}],"image":"exported_images\/00438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cole-Carpenter syndrome"}],"image":"exported_images\/00439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cole-Carpenter syndrome"}],"image":"exported_images\/00440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/00441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND"}],"image":"exported_images\/00442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND"}],"image":"exported_images\/00443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND"}],"image":"exported_images\/00444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Focal facial dermal dysplasia"}],"image":"exported_images\/00445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facial paresis, hereditary congenital"}],"image":"exported_images\/00446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facial paresis, hereditary congenital"}],"image":"exported_images\/00447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facial paresis, hereditary congenital"}],"image":"exported_images\/00448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facial paresis, hereditary congenital"}],"image":"exported_images\/00449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/00450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/00451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARBER-SAY SYNDROME; BBRSAY"}],"image":"exported_images\/00453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARBER-SAY SYNDROME; BBRSAY"}],"image":"exported_images\/00454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NANCE-HORAN SYNDROME; NHS"}],"image":"exported_images\/00455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NANCE-HORAN SYNDROME; NHS"}],"image":"exported_images\/00456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Central hypoventilation syndrome, congenital"}],"image":"exported_images\/00457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STEEL SYNDROME; STLS"}],"image":"exported_images\/00458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LACRIMOAURICULODENTODIGITAL SYNDROME; LADD"}],"image":"exported_images\/00459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fanconi anemia"}],"image":"exported_images\/00460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cole-Carpenter syndrome"}],"image":"exported_images\/00461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MCCUNE-ALBRIGHT SYNDROME; MAS"}],"image":"exported_images\/00462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DER WOUDE SYNDROME 1; VWS1"}],"image":"exported_images\/00463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DER WOUDE SYNDROME 1; VWS1"}],"image":"exported_images\/00464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/00465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/00466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/00467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/00468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/00469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/00470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/00471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE"}],"image":"exported_images\/00472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE"}],"image":"exported_images\/00473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3"}],"image":"exported_images\/00474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3"}],"image":"exported_images\/00475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACTL6A"}],"image":"exported_images\/00476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACTL6A"}],"image":"exported_images\/00477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54; DEE54"}],"image":"exported_images\/00478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Abnormality of the ear\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED"}],"image":"exported_images\/00479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Infantile liver failure syndrome"}],"image":"exported_images\/00480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Infantile liver failure syndrome"}],"image":"exported_images\/00481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Infantile liver failure syndrome"}],"image":"exported_images\/00482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Infantile liver failure syndrome"}],"image":"exported_images\/00483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Epilepsy, progressive myoclonic"}],"image":"exported_images\/00484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF"}],"image":"exported_images\/00485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF"}],"image":"exported_images\/00486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microphthalmia\n- Facial cleft\n- Bilateral cleft lip and palate\n- Aplasia\/Hypoplasia of the mandible\n- Ankyloblepharon\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARTSOCAS-PAPAS SYNDROME 1; BPS1"}],"image":"exported_images\/00487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mandibuloacral dysplasia with lipodystrophy"}],"image":"exported_images\/00488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MCCUNE-ALBRIGHT SYNDROME; MAS"}],"image":"exported_images\/00489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MCCUNE-ALBRIGHT SYNDROME; MAS"}],"image":"exported_images\/00490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/00499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARBER-SAY SYNDROME; BBRSAY"}],"image":"exported_images\/00500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin vermilion border\n- Low anterior hairline\n- Micrognathia\n- Low-set ears\n- Bulbous nose\n- Wide nose\n- Telecanthus\n- Ectropion\n- Dry skin\n- Hypertrichosis\n- Redundant skin\n- Inverted nipples\n- Microtia\n- Lipodystrophy\n- Epiblepharon\n- Extra concha fold\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARBER-SAY SYNDROME; BBRSAY"}],"image":"exported_images\/00501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Low anterior hairline\n- Hypertelorism\n- Hypoplasia of the maxilla\n- Abnormality of the auditory canal\n- Bulbous nose\n- Wide nose\n- Prominent nose\n- Ectropion\n- Widely spaced teeth\n- Hypertrichosis\n- Redundant skin\n- Hypoplastic nipples\n- Abnormal venous morphology\n- Mild global developmental delay\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARBER-SAY SYNDROME; BBRSAY"}],"image":"exported_images\/00502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad nasal tip\n- Sparse scalp hair\n- Thick nasal alae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ABLEPHARON-MACROSTOMIA SYNDROME; AMS"}],"image":"exported_images\/00503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad nasal tip\n- Sparse scalp hair\n- Thick nasal alae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ABLEPHARON-MACROSTOMIA SYNDROME; AMS"}],"image":"exported_images\/00504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR"}],"image":"exported_images\/00510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES"}],"image":"exported_images\/00511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES"}],"image":"exported_images\/00512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUENKE SYNDROME; MNKES"}],"image":"exported_images\/00513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CURRARINO SYNDROME"}],"image":"exported_images\/00514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CURRARINO SYNDROME"}],"image":"exported_images\/00515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/00517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I; MOPD1"}],"image":"exported_images\/00518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I; MOPD1"}],"image":"exported_images\/00519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/00520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/00521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/00522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/00523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/00524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/00525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"APERT SYNDROME"}],"image":"exported_images\/00526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/00527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/00528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/00529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/00530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial DNA depletion syndrome"}],"image":"exported_images\/00531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial DNA depletion syndrome"}],"image":"exported_images\/00532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF"}],"image":"exported_images\/00533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF"}],"image":"exported_images\/00534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF"}],"image":"exported_images\/00535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE"}],"image":"exported_images\/00536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DER WOUDE SYNDROME 1; VWS1"}],"image":"exported_images\/00537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DER WOUDE SYNDROME 1; VWS1"}],"image":"exported_images\/00538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIX2"}],"image":"exported_images\/00539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIX2"}],"image":"exported_images\/00540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1"}],"image":"exported_images\/00541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Desbuquois dysplasia"}],"image":"exported_images\/00542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Desbuquois dysplasia"}],"image":"exported_images\/00543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cole-Carpenter syndrome"}],"image":"exported_images\/00544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cole-Carpenter syndrome"}],"image":"exported_images\/00545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DDX23"}],"image":"exported_images\/00548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Focal facial dermal dysplasia"}],"image":"exported_images\/00549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Focal facial dermal dysplasia"}],"image":"exported_images\/00550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Focal facial dermal dysplasia"}],"image":"exported_images\/00551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CK SYNDROME; CKS"}],"image":"exported_images\/00552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CK SYNDROME; CKS"}],"image":"exported_images\/00553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/00554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, X-LINKED; OHDOX"}],"image":"exported_images\/00555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LEOPARD syndrome"}],"image":"exported_images\/00556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LEOPARD syndrome"}],"image":"exported_images\/00557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LEOPARD syndrome"}],"image":"exported_images\/00558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial complex V (ATP synthase) deficiency, nuclear type"}],"image":"exported_images\/00559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial complex V (ATP synthase) deficiency, nuclear type"}],"image":"exported_images\/00560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial complex V (ATP synthase) deficiency, nuclear type"}],"image":"exported_images\/00561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial complex V (ATP synthase) deficiency, nuclear type"}],"image":"exported_images\/00562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS"}],"image":"exported_images\/00563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED"}],"image":"exported_images\/00564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED"}],"image":"exported_images\/00565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35; MRXS35"}],"image":"exported_images\/00566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35; MRXS35"}],"image":"exported_images\/00567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35; MRXS35"}],"image":"exported_images\/00568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35; MRXS35"}],"image":"exported_images\/00569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS; MIGSB"}],"image":"exported_images\/00570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TONNE-KALSCHEUER SYNDROME; TOKAS"}],"image":"exported_images\/00571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TONNE-KALSCHEUER SYNDROME; TOKAS"}],"image":"exported_images\/00572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TONNE-KALSCHEUER SYNDROME; TOKAS"}],"image":"exported_images\/00573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TONNE-KALSCHEUER SYNDROME; TOKAS"}],"image":"exported_images\/00574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB-SHAFFER SYNDROME; LAMSHF"}],"image":"exported_images\/00575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichothiodystrophy"}],"image":"exported_images\/00576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichothiodystrophy"}],"image":"exported_images\/00577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PLXND1"}],"image":"exported_images\/00581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PLXND1"}],"image":"exported_images\/00582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PLXND1"}],"image":"exported_images\/00583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"REV3L"}],"image":"exported_images\/00584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"REV3L"}],"image":"exported_images\/00585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"REV3L"}],"image":"exported_images\/00586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"REV3L"}],"image":"exported_images\/00587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WARSAW BREAKAGE SYNDROME; WABS"}],"image":"exported_images\/00588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME; MICCAP"}],"image":"exported_images\/00589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME; MICCAP"}],"image":"exported_images\/00590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAJDU-CHENEY SYNDROME; HJCYS"}],"image":"exported_images\/00591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 7; MRT7"}],"image":"exported_images\/00592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/00593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/00594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL MICROSOMIA; CFM"}],"image":"exported_images\/00595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL MICROSOMIA; CFM"}],"image":"exported_images\/00596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL MICROSOMIA; CFM"}],"image":"exported_images\/00597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JAWAD SYNDROME; JWDS"}],"image":"exported_images\/00598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAGAMI-OGATA SYNDROME"}],"image":"exported_images\/00599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAGAMI-OGATA SYNDROME"}],"image":"exported_images\/00600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAGAMI-OGATA SYNDROME"}],"image":"exported_images\/00601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/00602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB-SHAFFER SYNDROME; LAMSHF"}],"image":"exported_images\/00603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB-SHAFFER SYNDROME; LAMSHF"}],"image":"exported_images\/00604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Facial asymmetry\n- Strabismus\n- Oligodontia\n- Dental malocclusion\n- Microdontia\n- Conical tooth\n- Atrophic, patchy alopecia\n- Persistence of primary teeth\n- Peripapillary chorioretinal atrophy\n- Thick nasal alae\n- High myopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBINOW-SORAUF SYNDROME"}],"image":"exported_images\/00606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBINOW-SORAUF SYNDROME"}],"image":"exported_images\/00607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SWEENEY-COX SYNDROME; SWCOS"}],"image":"exported_images\/00608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SWEENEY-COX SYNDROME; SWCOS"}],"image":"exported_images\/00609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DUANE-RADIAL RAY SYNDROME; DRRS"}],"image":"exported_images\/00610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DUANE-RADIAL RAY SYNDROME; DRRS"}],"image":"exported_images\/00611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DUANE-RADIAL RAY SYNDROME; DRRS"}],"image":"exported_images\/00612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DUANE-RADIAL RAY SYNDROME; DRRS"}],"image":"exported_images\/00613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED"}],"image":"exported_images\/00614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOXA2"}],"image":"exported_images\/00615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 38; MRD38"}],"image":"exported_images\/00616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 38; MRD38"}],"image":"exported_images\/00617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE; MRXSCH"}],"image":"exported_images\/00618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Warburg micro syndrome"}],"image":"exported_images\/00619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/00620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/00621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/00622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/00623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/00624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/00625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME; CFSMR"}],"image":"exported_images\/00626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME; CFSMR"}],"image":"exported_images\/00627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME; CFSMR"}],"image":"exported_images\/00628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS"}],"image":"exported_images\/00629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS"}],"image":"exported_images\/00630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS"}],"image":"exported_images\/00631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS"}],"image":"exported_images\/00632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRIAS SYNDROME"}],"image":"exported_images\/00633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ectodermal dysplasia (select examples)"}],"image":"exported_images\/00634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniometaphyseal dysplasia"}],"image":"exported_images\/00636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/00643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FILIPPI SYNDROME; FLPIS"}],"image":"exported_images\/00644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FILIPPI SYNDROME; FLPIS"}],"image":"exported_images\/00645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR"}],"image":"exported_images\/00646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR"}],"image":"exported_images\/00647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMMUNODEFICIENCY 23; IMD23"}],"image":"exported_images\/00648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMMUNODEFICIENCY 23; IMD23"}],"image":"exported_images\/00649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 2q37 DELETION SYNDROME"}],"image":"exported_images\/00651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 2q37 DELETION SYNDROME"}],"image":"exported_images\/00652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 2q37 DELETION SYNDROME"}],"image":"exported_images\/00653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/00657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/00660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Epicanthus\n- Microretrognathia\n- Long philtrum\n- Widow's peak\n- Low-set, posteriorly rotated ears\n- Preauricular skin tag\n- Thickened nuchal skin fold\n- Strabismus\n- Upslanted palpebral fissure\n- Blue sclerae\n- Diastasis recti\n- Ventricular septal defect\n- Atrial septal defect\n- Low posterior hairline\n- Sparse scalp hair\n- Highly arched eyebrow\n- Low-set nipples\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Mild global developmental delay\n- Moon facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SULEIMAN-EL-HATTAB SYNDROME; SULEHS"}],"image":"exported_images\/00661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dolichocephaly\n- Long face\n- Mixed hearing impairment\n- Narrow nose\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Arachnodactyly\n- Mitral valve prolapse\n- Arthrogryposis multiplex congenita\n- Long nose\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DEN ENDE-GUPTA SYNDROME; VDEGS"}],"image":"exported_images\/00662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Conductive hearing impairment\n- Ptosis\n- Blepharophimosis\n- Arachnodactyly\n- Plagiocephaly\n- Ventricular septal defect\n- Arthrogryposis multiplex congenita\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DEN ENDE-GUPTA SYNDROME; VDEGS"}],"image":"exported_images\/00663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY; NEDHSCA"}],"image":"exported_images\/00664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Cerebellar atrophy\n- Tremor\n- Abnormality of mitochondrial metabolism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY; NEDHSCA"}],"image":"exported_images\/00665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ATP9A"}],"image":"exported_images\/00666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Platyspondyly\n- Brachydactyly\n- Kyphoscoliosis\n- Disproportionate short-trunk short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spondylometaphyseal dysplasia"}],"image":"exported_images\/00667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Generalized non-motor (absence) seizure\n- Intellectual disability, moderate\n- Language impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 13; DEE13"}],"image":"exported_images\/00668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Hypertelorism\n- Low-set ears\n- Strabismus\n- Autism\n- Intellectual disability, moderate\n- EEG abnormality\n- Hypsarrhythmia\n- Epiblepharon of upper lid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70"}],"image":"exported_images\/00669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dolichocephaly\n- Global developmental delay\n- Downturned corners of mouth\n- Generalized joint laxity\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB4"}],"image":"exported_images\/00670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84; DEE84"}],"image":"exported_images\/00671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Broad face\n- Full cheeks\n- Short chin\n- Anteverted nares\n- Megalocornea\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/00672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Broad face\n- Full cheeks\n- Short chin\n- Anteverted nares\n- Megalocornea\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/00673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Brachycephaly\n- Wide anterior fontanel\n- Full cheeks\n- Hypertelorism\n- Micrognathia\n- Macrotia\n- Megalocornea\n- Proptosis\n- Kyphosis\n- Short palm\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/00674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Brachycephaly\n- Wide anterior fontanel\n- Full cheeks\n- Hypertelorism\n- Micrognathia\n- Megalocornea\n- Proptosis\n- Ventricular septal defect\n- Short palm\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/00675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Microcephaly\n- Protruding ear\n- Seizure\n- Scoliosis\n- Moderate postnatal growth retardation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB-SHAFFER SYNDROME; LAMSHF"}],"image":"exported_images\/00676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Long face\n- Mandibular prognathia\n- Triangular nasal tip\n- Developmental cataract\n- Optic nerve hypoplasia\n- Delayed speech and language development\n- Pectus carinatum\n- Delayed puberty\n- Decreased response to growth hormone stimulation test\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Cerebellar atrophy\n- Gait ataxia\n- Truncal ataxia\n- Increased serum lactate\n- Delayed skeletal maturation\n- Mild short stature\n- Limb muscle weakness\n- Mild global developmental delay\n- Increased intramyocellular lipid droplets\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAREL-YOON SYNDROME; HAYOS"}],"image":"exported_images\/00677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Atypical behavior\n- Autism\n- Pes planus\n- Intellectual disability, profound\n- Language impairment\n- Bowel incontinence\n- Thoracolumbar scoliosis\n- Talipes valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETTIGREW SYNDROME; PGS"}],"image":"exported_images\/00678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53; MRD53"}],"image":"exported_images\/00679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Intellectual disability\n- Multifocal epileptiform discharges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY; NEDEGE"}],"image":"exported_images\/00680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sparse eyelashes\n- Eczema\n- Palmoplantar keratoderma\n- Cutaneous photosensitivity\n- Lymphedema\n- Poikiloderma\n- Heat intolerance\n- Sparse scalp hair\n- Steatorrhea\n- Lower-limb joint contracture\n- Ichthyosis\n- Sparse hair\n- Distributed along Blaschko lines\n- Palmoplantar erythema\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/00681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Epicanthus\n- Narrow forehead\n- Long philtrum\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Hypothyroidism\n- Global developmental delay\n- Failure to thrive\n- Frontal bossing\n- Chiari malformation\n- Recurrent infections\n- Elevated hepatic transaminase\n- Inverted nipples\n- Short stature\n- Prominent nasal tip\n- Facial paralysis\n- High anterior hairline\n- Feeding difficulties\n- Enlarged cerebellum\n- Oral motor hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CYSTIC FIBROSIS; CF"}],"image":"exported_images\/00682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/00683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/00684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/00685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/00686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/00687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/00688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Obesity\n- Severe muscular hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES; IDDBCS"}],"image":"exported_images\/00689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High forehead\n- Anteverted nares\n- Proptosis\n- Talipes\n- Depressed nasal bridge\n- Sparse hair\n- Short distal phalanx of finger\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF"}],"image":"exported_images\/00690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Deeply set eye\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Motor delay\n- Dysphagia\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Global brain atrophy\n- Difficulty walking\n- Scoliosis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Glut1 deficiency syndrome"}],"image":"exported_images\/00691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Deeply set eye\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Motor delay\n- Dysphagia\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Global brain atrophy\n- Difficulty walking\n- Scoliosis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Glut1 deficiency syndrome"}],"image":"exported_images\/00692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Macrocephaly\n- Malar flattening\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Asthma\n- Drooling\n- Short nose\n- Impaired mastication\n- Severe expressive language delay\n- Oromotor apraxia\n- Speech articulation difficulties\n- Prominent forehead\n- Prominent digit pad\n- Severe receptive language delay\n- Clinodactyly of the 4th toe\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"}],"image":"exported_images\/00693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Macrocephaly\n- Malar flattening\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Asthma\n- Drooling\n- Short nose\n- Impaired mastication\n- Severe expressive language delay\n- Oromotor apraxia\n- Speech articulation difficulties\n- Prominent forehead\n- Prominent digit pad\n- Severe receptive language delay\n- Clinodactyly of the 4th toe\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"}],"image":"exported_images\/00694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Strabismus\n- Adducted thumb\n- Global developmental delay\n- Motor delay\n- Agenesis of corpus callosum\n- Lower limb spasticity\n- Ventriculomegaly\n- Delayed skeletal maturation\n- Thoracic scoliosis\n- Decreased body weight\n- Depressed nasal bridge\n- Contracture of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spastic paraplegia"}],"image":"exported_images\/00695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal lower lip morphology\n- Pointed chin\n- Short philtrum\n- Prominent supraorbital ridges\n- Broad forehead\n- Bulbous nose\n- Strabismus\n- Deeply set eye\n- Hypotelorism\n- Hyperactivity\n- Periorbital hyperpigmentation\n- Seizure\n- Gait disturbance\n- Sandal gap\n- Frontal bossing\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Sleep disturbance\n- Kyphosis\n- Depressed nasal bridge\n- 2-4 toe cutaneous syndactyly\n- Short metacarpal\n- Broad hallux\n- Short hallux\n- Abnormal third toe morphology\n- Abnormal fourth toe morphology\n- Short metatarsal\n- Abnormality of canine\n- Speech apraxia\n- Midface retrusion\n- Thick vermilion border\n- Finger clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JARID2"}],"image":"exported_images\/00696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Narrow forehead\n- Bulbous nose\n- Strabismus\n- Deeply set eye\n- Hypermetropia\n- Upslanted palpebral fissure\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Hyperreflexia\n- Poor suck\n- Chronic constipation\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETTIGREW SYNDROME; PGS"}],"image":"exported_images\/00697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Open mouth\n- Epicanthus\n- Smooth philtrum\n- Short philtrum\n- Synophrys\n- Seizure\n- Hypotonia\n- Motor delay\n- Areflexia\n- Absent speech\n- Drooling\n- EEG with polyspike wave complexes\n- Poor head control\n- Intellectual disability, severe\n- Epileptic spasm\n- EEG with generalized polyspikes\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84; DEE84"}],"image":"exported_images\/00698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Myopia\n- Delayed speech and language development\n- Global developmental delay\n- Joint hypermobility\n- Pes cavus\n- Poor gross motor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"}],"image":"exported_images\/00699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Velopharyngeal insufficiency\n- Pointed chin\n- Hypertelorism\n- Broad forehead\n- Micrognathia\n- Posteriorly rotated ears\n- Astigmatism\n- Strabismus\n- Downslanted palpebral fissures\n- Long eyelashes\n- Long palpebral fissure\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Hypernasal speech\n- Gastroesophageal reflux\n- Frontal upsweep of hair\n- Drooling\n- Unsteady gait\n- Hand tremor\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Attention deficit hyperactivity disorder\n- Slowed slurred speech\n- Axial hypotonia\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR DYSFUNCTION WITH VARIABLE COGNITIVE AND BEHAVIORAL ABNORMALITIES; CECBA"}],"image":"exported_images\/00700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Patent foramen ovale\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES; GDSBA"}],"image":"exported_images\/00701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Pointed chin\n- Hypertelorism\n- Wide nasal bridge\n- Esotropia\n- Widely spaced teeth\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Failure to thrive\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Hyperammonemia\n- Ventriculomegaly\n- Hyperhomocystinemia\n- Exaggerated cupid's bow\n- Prominent nasal tip\n- Sparse hair\n- Prominent forehead\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Methylmalonic aciduria and homocystinuria"}],"image":"exported_images\/00702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Intellectual disability\n- Seizure\n- Ataxia\n- Dysarthria\n- Global developmental delay\n- Pancreatitis\n- Cerebral cortical atrophy\n- Colitis\n- Appendicular hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY; NEDEGE"}],"image":"exported_images\/00703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Mandibular prognathia\n- Hypomimic face\n- Protruding ear\n- Deeply set eye\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Cyanosis\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Bradykinesia\n- Intellectual disability, profound\n- Generalized-onset seizure\n- Focal clonic seizure\n- Tetraparesis\n- Hypokinesia\n- Inability to walk\n- Kyphoscoliosis\n- Frontotemporal cerebral atrophy\n- Focal-onset seizure\n- Protruding tongue\n- EEG with focal spike waves\n- Clonic seizure\n- Staring gaze\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7; DEE7"}],"image":"exported_images\/00704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Mandibular prognathia\n- Hypomimic face\n- Protruding ear\n- Deeply set eye\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Cyanosis\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Bradykinesia\n- Intellectual disability, profound\n- Generalized-onset seizure\n- Focal clonic seizure\n- Tetraparesis\n- Hypokinesia\n- Inability to walk\n- Kyphoscoliosis\n- Frontotemporal cerebral atrophy\n- Focal-onset seizure\n- Protruding tongue\n- EEG with focal spike waves\n- Clonic seizure\n- Staring gaze\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7; DEE7"}],"image":"exported_images\/00705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Mandibular prognathia\n- Hypomimic face\n- Protruding ear\n- Deeply set eye\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Cyanosis\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Bradykinesia\n- Intellectual disability, profound\n- Generalized-onset seizure\n- Focal clonic seizure\n- Tetraparesis\n- Hypokinesia\n- Inability to walk\n- Kyphoscoliosis\n- Frontotemporal cerebral atrophy\n- Focal-onset seizure\n- Protruding tongue\n- EEG with focal spike waves\n- Clonic seizure\n- Staring gaze\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7; DEE7"}],"image":"exported_images\/00706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Facial asymmetry\n- Sensorineural hearing impairment\n- Telecanthus\n- Rod-cone dystrophy\n- Cataract\n- Nyctalopia\n- Dental crowding\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Language impairment\n- High, narrow palate\n- Kyphosis\n- Neck flexor weakness\n- Abnormal auditory evoked potentials\n- Reduced visual acuity\n- Congenital sensorineural hearing impairment\n- Underfolded helix\n- Large earlobe\n- Widened subarachnoid space\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Usher syndrome"}],"image":"exported_images\/00707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Wide nasal bridge\n- Choanal atresia\n- Broad nasal tip\n- Ectropion\n- Hypodontia\n- Delayed eruption of permanent teeth\n- Ventricular septal defect\n- Atrial septal defect\n- Mitral stenosis\n- Restrictive ventilatory defect\n- Highly arched eyebrow\n- Scoliosis\n- Sparse lateral eyebrow\n- Distichiasis\n- Midface retrusion\n- Hypoplastic aortic arch\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal duplication\n- Thin upper lip vermilion\n- Hydrocephalus\n- Brachycephaly\n- Microcephaly\n- Epicanthus\n- Pointed chin\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Posteriorly rotated ears\n- Macrotia\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Anteverted nares\n- Hypermetropia\n- Restlessness\n- Short attention span\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Pachygyria\n- Limitation of joint mobility\n- Pes cavus\n- Hypoplastic toenails\n- Ventriculomegaly\n- Short nose\n- Absent Achilles reflex\n- Absent patellar reflexes\n- Focal tonic seizure\n- EEG with abnormally slow frequencies\n- EEG with parietal sharp waves\n- Severe global developmental delay\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Lissencephaly"}],"image":"exported_images\/00709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal duplication\n- Thin upper lip vermilion\n- Hydrocephalus\n- Brachycephaly\n- Microcephaly\n- Epicanthus\n- Pointed chin\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Posteriorly rotated ears\n- Macrotia\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Anteverted nares\n- Hypermetropia\n- Restlessness\n- Short attention span\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Pachygyria\n- Limitation of joint mobility\n- Pes cavus\n- Hypoplastic toenails\n- Ventriculomegaly\n- Short nose\n- Absent Achilles reflex\n- Absent patellar reflexes\n- Focal tonic seizure\n- EEG with abnormally slow frequencies\n- EEG with parietal sharp waves\n- Severe global developmental delay\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Lissencephaly"}],"image":"exported_images\/00710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dolichocephaly\n- Broad forehead\n- High forehead\n- Upslanted palpebral fissure\n- Delayed eruption of permanent teeth\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Obesity\n- Hypoplastic toenails\n- Downturned corners of mouth\n- Cervical kyphosis\n- Mild short stature\n- Short metacarpal\n- Short metatarsal\n- Lung abscess\n- Increased size of the mandible\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/00711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad forehead\n- Long philtrum\n- Short neck\n- Upslanted palpebral fissure\n- Brachydactyly\n- Intellectual disability\n- Obesity\n- Hypoplastic toenails\n- Downturned corners of mouth\n- Short metacarpal\n- Short metatarsal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/00712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad forehead\n- Webbed neck\n- Brachydactyly\n- Intellectual disability\n- Obesity\n- Hypoplastic toenails\n- Short metacarpal\n- Short metatarsal\n- Increased size of the mandible\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/00713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Malar flattening\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Blepharitis\n- Cataract\n- Absent eyelashes\n- Dacryocystitis\n- Anodontia\n- Hypoplastic toenails\n- Weight loss\n- Bilateral cleft lip and palate\n- Long nose\n- Scarring alopecia of scalp\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Malar flattening\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Blepharitis\n- Cataract\n- Absent eyelashes\n- Dacryocystitis\n- Anodontia\n- Hypoplastic toenails\n- Weight loss\n- Bilateral cleft lip and palate\n- Long nose\n- Scarring alopecia of scalp\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydroureter\n- Micrognathia\n- Macrotia\n- Protruding ear\n- Prominent nasal bridge\n- Hypermetropia\n- Long palpebral fissure\n- Autism\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Achilles tendon contracture\n- Sandal gap\n- Deep philtrum\n- Aortic aneurysm\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Bilateral single transverse palmar creases\n- Ectropion of lower eyelids\n- Broad hallux\n- Ankyloglossia\n- Midsystolic murmur\n- Anteverted ears\n- obsolete Toe walking\n- Abnormality of the supraorbital ridges\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAF4"}],"image":"exported_images\/00716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Short philtrum\n- Prominent nasal bridge\n- Prominent nose\n- Synophrys\n- Delayed speech and language development\n- Gait disturbance\n- Lower limb spasticity\n- Highly arched eyebrow\n- Lumbar hyperlordosis\n- Thoracolumbar scoliosis\n- Clinodactyly of the 5th finger\n- Knee flexion contracture\n- Cerebellar vermis atrophy\n- Lower limb hypertonia\n- Inferior cerebellar vermis hypoplasia\n- Clinodactyly of the 3rd toe\n- Clinodactyly of the 4th toe\n- Thick vermilion border\n- Tip-toe gait\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAF4"}],"image":"exported_images\/00717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long philtrum\n- Posteriorly rotated ears\n- Macrotia\n- Prominent nasal bridge\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Deeply set eye\n- Hypermetropia\n- Thick eyebrow\n- Abnormality of the ear\n- Atopic dermatitis\n- Intellectual disability, mild\n- Joint hypermobility\n- Deep philtrum\n- Recurrent respiratory infections\n- Highly arched eyebrow\n- Short nose\n- Few cafe-au-lait spots\n- Epiblepharon\n- Emotional hypersensitivity\n- Shyness\n- Abnormality of the maxillary sinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAF4"}],"image":"exported_images\/00718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Wide nasal bridge\n- Anteverted nares\n- Thick eyebrow\n- Widely spaced teeth\n- Autistic behavior\n- Self-mutilation\n- Delayed speech and language development\n- Pes planus\n- Deep philtrum\n- Sleep disturbance\n- Depressed nasal bridge\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Abnormal helix morphology\n- Simple febrile seizure\n- Pica\n- Self hugging\n- obsolete Toe walking\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAF4"}],"image":"exported_images\/00719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Tall stature\n- Cleft palate\n- Thin upper lip vermilion\n- Retrognathia\n- Broad philtrum\n- Hearing impairment\n- Recurrent otitis media\n- Prominent nasal bridge\n- Thick eyebrow\n- Oligodontia\n- Delayed speech and language development\n- Narrow chest\n- Melanocytic nevus\n- Acne\n- Prominent fingertip pads\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Limited elbow extension\n- Slender build\n- Constipation\n- Drooling\n- Intellectual disability, moderate\n- Expressive language delay\n- Highly arched eyebrow\n- Scoliosis\n- Kyphosis\n- Long nose\n- Deviated nasal septum\n- Abnormality of the middle ear ossicles\n- Overfolding of the superior helices\n- 2-3 toe syndactyly\n- Oromotor apraxia\n- Feeding difficulties in infancy\n- Short finger\n- Interphalangeal thumb joint contracture\n- Speech apraxia\n- Flexion contracture of finger\n- Abnormality of the tympanic membrane\n- Narrow palpebral fissure\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAF4"}],"image":"exported_images\/00720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low anterior hairline\n- Prominent nose\n- Thick eyebrow\n- Synophrys\n- Hirsutism\n- Intellectual disability\n- 2-3 toe syndactyly\n- Abnormal columella morphology\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI-YUAN SYNDROME; ALYUS"}],"image":"exported_images\/00721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low anterior hairline\n- Prominent nose\n- Thick eyebrow\n- Synophrys\n- Hirsutism\n- Intellectual disability\n- 2-3 toe syndactyly\n- Abnormal columella morphology\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI-YUAN SYNDROME; ALYUS"}],"image":"exported_images\/00722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dolichocephaly\n- Hypertelorism\n- Micrognathia\n- Strabismus\n- Downslanted palpebral fissures\n- Optic nerve hypoplasia\n- Carious teeth\n- Microdontia\n- Pectus carinatum\n- Global developmental delay\n- Intrauterine growth retardation\n- Severe postnatal growth retardation\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME A; CSA"}],"image":"exported_images\/00723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Horseshoe kidney\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Bulbous nose\n- Visual impairment\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Decreased response to growth hormone stimulation test\n- Seizure\n- Hypotonia\n- Cerebellar atrophy\n- Abnormal corpus callosum morphology\n- Absent speech\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Abnormal caudate nucleus morphology\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Sparse lateral eyebrow\n- Bilateral single transverse palmar creases\n- Mild neurosensory hearing impairment\n- Anterior pituitary hypoplasia\n- Intellectual disability, severe\n- Severe global developmental delay\n- Infantile spasms\n- Unilateral cryptorchidism\n- Exodeviation\n- Mild myopia\n- Sleep onset insomnia\n- Maintenance insomnia\n- Mild hypermetropia\n- Unilateral cleft lip\n- Unilateral cleft palate\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB"}],"image":"exported_images\/00724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34; MRXS34"}],"image":"exported_images\/00725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Brachycephaly\n- Hypertelorism\n- Short philtrum\n- Recurrent otitis media\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Optic nerve hypoplasia\n- Macrodontia of permanent maxillary central incisor\n- Pallor\n- Acrocyanosis\n- Adducted thumb\n- Tapered finger\n- Global developmental delay\n- Areflexia\n- Myoclonus\n- Absent speech\n- Joint hypermobility\n- Growth delay\n- Widely-spaced maxillary central incisors\n- Asplenia\n- Bilateral talipes equinovarus\n- Hyperconvex fingernails\n- Poor suck\n- Hypothermia\n- Low posterior hairline\n- Frontal upsweep of hair\n- Cavum septum pellucidum\n- Limb hypertonia\n- Polyphagia\n- Kyphosis\n- Sudden episodic apnea\n- Thoracic scoliosis\n- Short palm\n- Intermittent hyperventilation\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Ankle flexion contracture\n- Index finger dermatoglyphic radial loop\n- Ridged fingernail\n- Microtia\n- Short finger\n- Abnormal optic disc morphology\n- Exodeviation\n- Howell-Jolly bodies\n- Subglottic laryngitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1"}],"image":"exported_images\/00726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Hypertelorism\n- Short philtrum\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Macrodontia of permanent maxillary central incisor\n- Pallor\n- Hypotonia\n- Global developmental delay\n- Hyperreflexia\n- Growth delay\n- Widely-spaced maxillary central incisors\n- Hyperconvex fingernails\n- Gastroesophageal reflux\n- Low posterior hairline\n- Frontal upsweep of hair\n- Polyphagia\n- Clinodactyly of the 5th finger\n- Short palm\n- Depressed nasal bridge\n- Increased dermatoglyphic whorls\n- Index finger dermatoglyphic radial loop\n- Ridged fingernail\n- Microtia\n- Bilateral cryptorchidism\n- Short finger\n- Exodeviation\n- Reduced blood folate concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1"}],"image":"exported_images\/00727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Delayed puberty\n- Increased circulating prolactin concentration\n- Shield chest\n- Melanocytic nevus\n- Multiple lentigines\n- Numerous nevi\n- Tetralogy of Fallot\n- Curly hair\n- Cubitus valgus\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Profuse pigmented skin lesions\n- Wide intermamillary distance\n- Epidermal hyperkeratosis\n- Dyslexia\n- Right bundle branch block\n- Mild myopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LEOPARD syndrome"}],"image":"exported_images\/00728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Facial asymmetry\n- Strabismus\n- Ptosis\n- Proptosis\n- Long eyelashes\n- Axillary pterygium\n- Camptodactyly of 2nd-5th fingers\n- Intellectual disability, mild\n- Camptodactyly of toe\n- Short stature\n- Curly eyelashes\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS"}],"image":"exported_images\/00729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Facial asymmetry\n- Strabismus\n- Ptosis\n- Proptosis\n- Long eyelashes\n- Axillary pterygium\n- Camptodactyly of 2nd-5th fingers\n- Intellectual disability, mild\n- Camptodactyly of toe\n- Short stature\n- Curly eyelashes\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS"}],"image":"exported_images\/00730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mandibuloacral dysplasia with lipodystrophy"}],"image":"exported_images\/00731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Full cheeks\n- Temporomandibular joint ankylosis\n- Question mark ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Auriculocondylar syndrome"}],"image":"exported_images\/00732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Full cheeks\n- Temporomandibular joint ankylosis\n- Question mark ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Auriculocondylar syndrome"}],"image":"exported_images\/00733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormality of the skin\n- Lissencephaly\n- Flexion contracture\n- Severe intrauterine growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Neu-Laxova syndrome"}],"image":"exported_images\/00734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Brachycephaly\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Myopia\n- Hemangioma\n- Seizure\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Reduced tendon reflexes\n- Absent speech\n- Short columella\n- Deep philtrum\n- Constipation\n- Gastroesophageal reflux\n- Sleep disturbance\n- Developmental regression\n- EEG with polyspike wave complexes\n- Downturned corners of mouth\n- Recurrent infections\n- Bruxism\n- Depressed nasal bridge\n- Thick corpus callosum\n- Thick vermilion border\n- Myoclonic seizure\n- Recurrent hand flapping\n- Coldness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/00735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Broad forehead\n- Abnormal repetitive mannerisms\n- Short attention span\n- Hypotonia\n- Global developmental delay\n- Deep philtrum\n- Broad-based gait\n- Delayed gross motor development\n- Generalized-onset seizure\n- Drooling\n- Sleep disturbance\n- Poor coordination\n- EEG with polyspike wave complexes\n- Abnormal cerebral white matter morphology\n- Downturned corners of mouth\n- Bruxism\n- Depressed nasal bridge\n- Low hanging columella\n- Tented upper lip vermilion\n- Feeding difficulties\n- Thick vermilion border\n- Scaphocephaly\n- Recurrent hand flapping\n- Tongue thrusting\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/00736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Broad forehead\n- Abnormal repetitive mannerisms\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Joint hypermobility\n- Deep philtrum\n- Constipation\n- Gastroesophageal reflux\n- Delayed gross motor development\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Downturned corners of mouth\n- Recurrent infections\n- Bruxism\n- Depressed nasal bridge\n- Low hanging columella\n- Tented upper lip vermilion\n- Posterior plagiocephaly\n- EEG with parietal focal spike waves\n- Stereotypical hand wringing\n- Mild myopia\n- EEG with temporal epileptiform discharges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/00737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Broad forehead\n- Abnormal repetitive mannerisms\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Joint hypermobility\n- Deep philtrum\n- Constipation\n- Gastroesophageal reflux\n- Delayed gross motor development\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Downturned corners of mouth\n- Recurrent infections\n- Bruxism\n- Depressed nasal bridge\n- Low hanging columella\n- Tented upper lip vermilion\n- Posterior plagiocephaly\n- EEG with parietal focal spike waves\n- Stereotypical hand wringing\n- Mild myopia\n- EEG with temporal epileptiform discharges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/00738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Amblyopia\n- Autism\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Hirsutism\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- Broad-based gait\n- Cortical dysplasia\n- Peripheral retinal avascularization\n- Subependymal nodules\n- Nummular eczema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/00739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Amblyopia\n- Autism\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Hirsutism\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- Broad-based gait\n- Cortical dysplasia\n- Peripheral retinal avascularization\n- Subependymal nodules\n- Nummular eczema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/00740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Hypertelorism\n- Square face\n- Short philtrum\n- Atypical behavior\n- Seizure\n- Myoclonus\n- Bilateral tonic-clonic seizure\n- Intellectual disability, moderate\n- EEG with polyspike wave complexes\n- Highly arched eyebrow\n- Slowed slurred speech\n- Myoclonic absence seizure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Hypertelorism\n- Square face\n- Short philtrum\n- Atypical behavior\n- Seizure\n- Myoclonus\n- Bilateral tonic-clonic seizure\n- Intellectual disability, moderate\n- EEG with polyspike wave complexes\n- Highly arched eyebrow\n- Slowed slurred speech\n- Myoclonic absence seizure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Underdeveloped nasal alae\n- Astigmatism\n- Long eyelashes\n- Myopia\n- Upslanted palpebral fissure\n- Atypical behavior\n- Depression\n- Aggressive behavior\n- Anxiety\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Growth delay\n- Narrow foot\n- Truncal obesity\n- Bilateral tonic-clonic seizure\n- Generalized-onset seizure\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Narrow palm\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Underdeveloped nasal alae\n- Astigmatism\n- Long eyelashes\n- Myopia\n- Upslanted palpebral fissure\n- Atypical behavior\n- Depression\n- Aggressive behavior\n- Anxiety\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Growth delay\n- Narrow foot\n- Truncal obesity\n- Bilateral tonic-clonic seizure\n- Generalized-onset seizure\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Narrow palm\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Underdeveloped nasal alae\n- Astigmatism\n- Long eyelashes\n- Myopia\n- Upslanted palpebral fissure\n- Atypical behavior\n- Depression\n- Aggressive behavior\n- Anxiety\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Growth delay\n- Narrow foot\n- Truncal obesity\n- Bilateral tonic-clonic seizure\n- Generalized-onset seizure\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Narrow palm\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Underdeveloped nasal alae\n- Astigmatism\n- Long eyelashes\n- Myopia\n- Upslanted palpebral fissure\n- Atypical behavior\n- Depression\n- Aggressive behavior\n- Anxiety\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Growth delay\n- Narrow foot\n- Truncal obesity\n- Bilateral tonic-clonic seizure\n- Generalized-onset seizure\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Narrow palm\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Mandibular prognathia\n- Strabismus\n- Widely spaced teeth\n- Autistic behavior\n- Short attention span\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait ataxia\n- Abnormality of speech or vocalization\n- Hyperactive deep tendon reflexes\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Frontal bossing\n- Chiari malformation\n- Bruxism\n- Decreased body weight\n- Secondary microcephaly\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Frontal bossing\n- Chiari malformation\n- Bruxism\n- Decreased body weight\n- Secondary microcephaly\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Bulbous nose\n- Wide nasal bridge\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Frontal bossing\n- Bruxism\n- Decreased body weight\n- Secondary microcephaly\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Bulbous nose\n- Wide nasal bridge\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Intrauterine growth retardation\n- Frontal bossing\n- Bruxism\n- Decreased body weight\n- Secondary microcephaly\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/00751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Febrile seizure (within the age range of 3 months to 6 years)\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY; NEDHSCA"}],"image":"exported_images\/00752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/00753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/00754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low anterior hairline\n- Convex nasal ridge\n- Thick eyebrow\n- Synophrys\n- Abnormality of the thenar eminence\n- Seizure\n- Global developmental delay\n- Brisk reflexes\n- Bilateral tonic-clonic seizure\n- Intellectual disability, moderate\n- Kyphosis\n- Mild short stature\n- Microtia\n- Abnormality of the hypothenar eminence\n- Overlapping fingers\n- Clinodactyly\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHUKLA-VERNON SYNDROME; SHUVER"}],"image":"exported_images\/00755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Abnormality of head or neck\n- Abnormality of the nervous system\n- Abnormality of prenatal development or birth\n- Global developmental delay\n- Abnormal heart morphology\n- Abnormality of the thoracic cavity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/00756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Abnormality of head or neck\n- Abnormality of the nervous system\n- Abnormality of prenatal development or birth\n- Global developmental delay\n- Abnormal heart morphology\n- Abnormality of the thoracic cavity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/00757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Abnormality of head or neck\n- Abnormality of the nervous system\n- Abnormal heart morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/00758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of head or neck\n- Abnormality of the nervous system\n- Abnormality of prenatal development or birth\n- Abnormality of the integument\n- Abnormality of the cardiovascular system\n- Nasogastric tube feeding in infancy\n- Abnormality of limbs\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA; CHDED"}],"image":"exported_images\/00759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS"}],"image":"exported_images\/00760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS"}],"image":"exported_images\/00761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS"}],"image":"exported_images\/00762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Facial asymmetry\n- Strabismus\n- Oligodontia\n- Dental malocclusion\n- Microdontia\n- Conical tooth\n- Atrophic, patchy alopecia\n- Persistence of primary teeth\n- Peripapillary chorioretinal atrophy\n- Thick nasal alae\n- High myopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/00763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad nasal tip\n- Sparse scalp hair\n- Thick nasal alae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ABLEPHARON-MACROSTOMIA SYNDROME; AMS"}],"image":"exported_images\/00764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG"}],"image":"exported_images\/00765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG"}],"image":"exported_images\/00766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/00767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/00768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/00769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 2q37 DELETION SYNDROME"}],"image":"exported_images\/00770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 1p36 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/00771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ASPARAGINE SYNTHETASE DEFICIENCY; ASNSD"}],"image":"exported_images\/00772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA"}],"image":"exported_images\/00773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Epilepsy, progressive myoclonic"}],"image":"exported_images\/00774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteopetrosis, autosomal recessive"}],"image":"exported_images\/00775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteopetrosis, autosomal recessive"}],"image":"exported_images\/00776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial DNA depletion syndrome"}],"image":"exported_images\/00777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteopetrosis, autosomal recessive"}],"image":"exported_images\/00778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47"}],"image":"exported_images\/00779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART; NEDBEH"}],"image":"exported_images\/00780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Retrognathia\n- Oval face\n- Long philtrum\n- Macrotia\n- Strabismus\n- Long palpebral fissure\n- Conjunctival icterus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CIMDAG SYNDROME; CIMDAG"}],"image":"exported_images\/00781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Retrognathia\n- Oval face\n- Long philtrum\n- Macrotia\n- Strabismus\n- Long palpebral fissure\n- Conjunctival icterus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CIMDAG SYNDROME; CIMDAG"}],"image":"exported_images\/00782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CIMDAG SYNDROME; CIMDAG"}],"image":"exported_images\/00783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Large hands\n- Intellectual disability, mild\n- Thoracic scoliosis\n- S-shaped palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN-GIBSON SYNDROME; COGIS"}],"image":"exported_images\/00784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Intellectual disability\n- Global developmental delay\n- Failure to thrive\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RADIO-TARTAGLIA SYNDROME; RATARS"}],"image":"exported_images\/00785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Short stature\n- Maxillozygomatic hypoplasia\n- Anotia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN"}],"image":"exported_images\/00786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Facial hypotonia\n- High forehead\n- Macrotia\n- Anteverted nares\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Generalized hypotonia\n- Delayed gross motor development\n- Axial hypotonia\n- Intellectual disability, severe\n- Vascular skin abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59"}],"image":"exported_images\/00787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Facial hypotonia\n- High forehead\n- Macrotia\n- Anteverted nares\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Generalized hypotonia\n- Delayed gross motor development\n- Axial hypotonia\n- Intellectual disability, severe\n- Vascular skin abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59"}],"image":"exported_images\/00788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Abnormality of the face\n- Low anterior hairline\n- Smooth philtrum\n- Micrognathia\n- Bulbous nose\n- Short neck\n- Strabismus\n- Abnormal electroretinogram\n- Proptosis\n- Long eyelashes\n- Thick eyebrow\n- Long palpebral fissure\n- Nystagmus\n- Syndactyly\n- Intellectual disability\n- Hepatosplenomegaly\n- Failure to thrive\n- Intrauterine growth retardation\n- Pancytopenia\n- Anemia\n- 2-3 toe syndactyly\n- Polydactyly\n- Abnormal renal cortex morphology\n- Thick hair\n- Abnormal renal medulla morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEGCAGS SYNDROME; DEGCAGS"}],"image":"exported_images\/00789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Ambiguous genitalia, male\n- Hypospadias\n- Wide mouth\n- Thin upper lip vermilion\n- Thin vermilion border\n- Coarse facial features\n- Posteriorly rotated ears\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hypotelorism\n- Long palpebral fissure\n- Sacral dimple\n- Abnormally large globe\n- Hypotonia\n- Global developmental delay\n- Generalized hypotonia\n- Cerebellar vermis hypoplasia\n- Polyhydramnios\n- Premature birth\n- Abnormal heart morphology\n- Pulmonic stenosis\n- Ventriculomegaly\n- Hyperbilirubinemia\n- Short long bone\n- Short nose\n- 2-3 toe syndactyly\n- Respiratory failure requiring assisted ventilation\n- Wide intermamillary distance\n- Cerebral hypomyelination\n- Absent thumb\n- Broad eyebrow\n- Frontal hirsutism\n- Nasogastric tube feeding\n- Reduced blood folate concentration\n- Sepsis\n- Ductus venosus agenesis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEGCAGS SYNDROME; DEGCAGS"}],"image":"exported_images\/00790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Ambiguous genitalia, male\n- Hypospadias\n- Wide mouth\n- Thin upper lip vermilion\n- Thin vermilion border\n- Coarse facial features\n- Posteriorly rotated ears\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hypotelorism\n- Long palpebral fissure\n- Sacral dimple\n- Abnormally large globe\n- Hypotonia\n- Global developmental delay\n- Generalized hypotonia\n- Cerebellar vermis hypoplasia\n- Polyhydramnios\n- Premature birth\n- Abnormal heart morphology\n- Pulmonic stenosis\n- Ventriculomegaly\n- Hyperbilirubinemia\n- Short long bone\n- Short nose\n- 2-3 toe syndactyly\n- Respiratory failure requiring assisted ventilation\n- Wide intermamillary distance\n- Cerebral hypomyelination\n- Absent thumb\n- Broad eyebrow\n- Frontal hirsutism\n- Nasogastric tube feeding\n- Reduced blood folate concentration\n- Sepsis\n- Ductus venosus agenesis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEGCAGS SYNDROME; DEGCAGS"}],"image":"exported_images\/00791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ASPARAGINE SYNTHETASE DEFICIENCY; ASNSD"}],"image":"exported_images\/00792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ASPARAGINE SYNTHETASE DEFICIENCY; ASNSD"}],"image":"exported_images\/00793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anxiety\n- Seizure\n- Paroxysmal dystonia\n- Expressive language delay\n- Clinodactyly of the 5th finger\n- Atonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cerebral creatine deficiency syndrome"}],"image":"exported_images\/00794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE; SEMDIST"}],"image":"exported_images\/00795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE; SEMDIST"}],"image":"exported_images\/00796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Coarse facial features\n- Prominent superficial veins\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/00798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Protruding ear\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WRINKLY SKIN SYNDROME; WSS"}],"image":"exported_images\/00799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Global developmental delay\n- Generalized hypotonia\n- Generalized hypopigmentation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Griscelli syndrome"}],"image":"exported_images\/00800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH, DYSMORPHIC FACIES, AND VARIABLE SKELETAL ANOMALIES; IDNADFS"}],"image":"exported_images\/00801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50"}],"image":"exported_images\/00802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50"}],"image":"exported_images\/00803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50"}],"image":"exported_images\/00804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50"}],"image":"exported_images\/00805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES; GDSBA"}],"image":"exported_images\/00806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Strabismus\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Plagiocephaly\n- Joint hypermobility\n- Talipes\n- Labial adhesion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES; GDSBA"}],"image":"exported_images\/00807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13"}],"image":"exported_images\/00808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13"}],"image":"exported_images\/00809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Hydronephrosis\n- Macrocephaly\n- Exotropia\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Tremor\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Drooling\n- Clinodactyly of the 5th finger\n- Recurrent pneumonia\n- EEG with spike-wave complexes\n- Prominent forehead\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PPFIA3"}],"image":"exported_images\/00810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Strabismus\n- Exotropia\n- Widely spaced teeth\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Dysarthria\n- Spastic diplegia\n- Dystonia\n- Absent speech\n- Myopathic facies\n- Gait ataxia\n- Depressed nasal bridge\n- Lower limb hypertonia\n- Diffuse white matter abnormalities\n- Protruding tongue\n- Prominent forehead\n- Severe global developmental delay\n- Feeding difficulties\n- Thick vermilion border\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PPFIA3"}],"image":"exported_images\/00811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Diamond-Blackfan anemia"}],"image":"exported_images\/00812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Diamond-Blackfan anemia"}],"image":"exported_images\/00813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Diamond-Blackfan anemia"}],"image":"exported_images\/00814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/00815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Downslanted palpebral fissures\n- Cutis laxa\n- Brittle hair\n- Short nose\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/00816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Downslanted palpebral fissures\n- Cutis laxa\n- Brittle hair\n- Short nose\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/00817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/00818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/00819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Round face\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Laryngomalacia\n- Sparse scalp hair\n- CNS hypomyelination\n- Prominent metopic ridge\n- Prolonged neonatal jaundice\n- High anterior hairline\n- Intellectual disability, severe\n- Gastrostomy tube feeding in infancy\n- Maintenance insomnia\n- Terminal insomnia\n- Limb tremor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES; NEDHYMS"}],"image":"exported_images\/00820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Kyphoscoliosis\n- Disproportionate short stature\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spondyloepimetaphyseal dysplasia with joint laxity"}],"image":"exported_images\/00821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Spondyloepiphyseal dysplasia\n- Disproportionate short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC"}],"image":"exported_images\/00822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Spondyloepiphyseal dysplasia\n- Disproportionate short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC"}],"image":"exported_images\/00823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUJAN-FRYNS TYPE; MRXSLF"}],"image":"exported_images\/00824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EMANUEL SYNDROME"}],"image":"exported_images\/00825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Subependymal cysts\n- Shagreen patch\n- Angiofibromas\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/00826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Deeply set eye\n- Global developmental delay\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 1p36 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/00827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C3"}],"image":"exported_images\/00828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C3"}],"image":"exported_images\/00829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Disproportionate short stature\n- Rhizomelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/00830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C3"}],"image":"exported_images\/00831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C3"}],"image":"exported_images\/00832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C3"}],"image":"exported_images\/00833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C9"}],"image":"exported_images\/00834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C9"}],"image":"exported_images\/00835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormality of the skeletal system\n- Spondyloepimetaphyseal dysplasia\n- Genu valgum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE; SEMDIST"}],"image":"exported_images\/00836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Spondyloepimetaphyseal dysplasia\n- Genu varum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE; SEMDIST"}],"image":"exported_images\/00837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Disproportionate short stature\n- Rhizomelic arm shortening\n- Rhizomelic leg shortening\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/00838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Pursed lips\n- Myotonia\n- Skeletal dysplasia\n- Disproportionate short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1"}],"image":"exported_images\/00839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Aortic root aneurysm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFAN SYNDROME; MFS"}],"image":"exported_images\/00840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Malar flattening\n- Arachnodactyly\n- Pes planus\n- Aortic root aneurysm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFAN SYNDROME; MFS"}],"image":"exported_images\/00841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Renal cyst\n- Specific learning disability\n- Shagreen patch\n- Angiofibromas\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/00842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Brachydactyly\n- Acromesomelia\n- Severe short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Acromesomelic dysplasia"}],"image":"exported_images\/00843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Broad forehead\n- Hearing impairment\n- Stenosis of the external auditory canal\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 18q DELETION SYNDROME"}],"image":"exported_images\/00844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC"}],"image":"exported_images\/00845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC"}],"image":"exported_images\/00846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cutis laxa\n- Intellectual disability\n- Abnormal corpus callosum morphology\n- Intrauterine growth retardation\n- Athetosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WRINKLY SKIN SYNDROME; WSS"}],"image":"exported_images\/00847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the face\n- Micrognathia\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I; MOPD1"}],"image":"exported_images\/00848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RECQL"}],"image":"exported_images\/00849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RECQL"}],"image":"exported_images\/00850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRPM3"}],"image":"exported_images\/00851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRPM3"}],"image":"exported_images\/00852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NAE1"}],"image":"exported_images\/00853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NAE1"}],"image":"exported_images\/00854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NAE1"}],"image":"exported_images\/00855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PGM2L1"}],"image":"exported_images\/00856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PGM2L1"}],"image":"exported_images\/00857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/00858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/00859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/00860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/00861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/00862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRA10AC1"}],"image":"exported_images\/00863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRA10AC1"}],"image":"exported_images\/00864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRA10AC1"}],"image":"exported_images\/00865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRA10AC1"}],"image":"exported_images\/00866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Cataract\n- Keratoconus\n- Multiple lentigines\n- Joint hypermobility\n- Arthralgia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LEOPARD syndrome"}],"image":"exported_images\/00867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Movement abnormality of the tongue\n- Nystagmus\n- Delayed speech and language development\n- Pectus carinatum\n- Cafe-au-lait spot\n- Dry skin\n- Pallor\n- Hypotonia\n- Gait disturbance\n- Reduced tendon reflexes\n- Gait ataxia\n- Drooling\n- Recurrent infections\n- Kyphoscoliosis\n- Kyphosis\n- Interstitial pneumonitis\n- Scaphoid abdomen\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ATAXIA-TELANGIECTASIA; AT"}],"image":"exported_images\/00868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Movement abnormality of the tongue\n- Nystagmus\n- Delayed speech and language development\n- Pectus carinatum\n- Cafe-au-lait spot\n- Dry skin\n- Pallor\n- Hypotonia\n- Gait disturbance\n- Reduced tendon reflexes\n- Gait ataxia\n- Drooling\n- Recurrent infections\n- Kyphoscoliosis\n- Kyphosis\n- Interstitial pneumonitis\n- Scaphoid abdomen\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ATAXIA-TELANGIECTASIA; AT"}],"image":"exported_images\/00869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZSCAN10"}],"image":"exported_images\/00870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZSCAN10"}],"image":"exported_images\/00871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gait disturbance\n- Arthritis\n- Small for gestational age\n- Diarrhea\n- Recurrent respiratory infections\n- Lymphadenopathy\n- Decreased circulating IgA level\n- Decreased circulating IgG level\n- Elevated circulating alpha-fetoprotein concentration\n- Localized skin lesion\n- Neonatal asphyxia\n- Intraventricular hemorrhage\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RIDDLE SYNDROME; RIDL"}],"image":"exported_images\/00872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gait disturbance\n- Arthritis\n- Small for gestational age\n- Diarrhea\n- Recurrent respiratory infections\n- Lymphadenopathy\n- Decreased circulating IgA level\n- Decreased circulating IgG level\n- Elevated circulating alpha-fetoprotein concentration\n- Localized skin lesion\n- Neonatal asphyxia\n- Intraventricular hemorrhage\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RIDDLE SYNDROME; RIDL"}],"image":"exported_images\/00873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long penis\n- Narrow mouth\n- Low anterior hairline\n- High forehead\n- Low-set ears\n- Downslanted palpebral fissures\n- Growth delay\n- Low posterior hairline\n- Short stature\n- Decreased body weight\n- Low hanging columella\n- Limb undergrowth\n- Short palpebral fissure\n- Webbed penis\n- Irregular dentition\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS"}],"image":"exported_images\/00874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Spondyloepiphyseal dysplasia\n- Disproportionate short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC"}],"image":"exported_images\/00875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mask-like facies\n- Conjunctival telangiectasia\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ATAXIA-TELANGIECTASIA; AT"}],"image":"exported_images\/00876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Otitis media\n- Sensorineural hearing impairment\n- Abnormality of visual evoked potentials\n- Membranoproliferative glomerulonephritis\n- Atopic dermatitis\n- Intellectual disability\n- Ataxia\n- Dysarthria\n- Myoclonus\n- Recurrent skin infections\n- Polycythemia\n- Pneumonia\n- Bronchiectasis\n- EEG abnormality\n- Vasculitis\n- Scoliosis\n- Allergic rhinitis\n- Increased circulating IgE level\n- Increased circulating IgG level\n- Aortic arch aneurysm\n- CNS demyelination\n- Intervertebral disc degeneration\n- Erythema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMMUNODEFICIENCY 23; IMD23"}],"image":"exported_images\/00877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Eczema\n- Eczematoid dermatitis\n- Skin rash\n- Pruritus\n- Failure to thrive\n- Chronic diarrhea\n- Pneumonia\n- Osteomyelitis\n- Recurrent herpes\n- Erythema\n- Wheezing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMMUNODEFICIENCY 23; IMD23"}],"image":"exported_images\/00878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"APERT SYNDROME"}],"image":"exported_images\/00879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Foot polydactyly\n- Frontal bossing\n- Calcification of falx cerebri\n- Odontogenic keratocysts of the jaw\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASAL CELL NEVUS SYNDROME; BCNS"}],"image":"exported_images\/00880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Spasticity\n- Dysarthria\n- Global developmental delay\n- Dystonia\n- Dysphagia\n- Infantile axial hypotonia\n- Abnormal circulating thyroid hormone concentration\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/00881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Spasticity\n- Dysarthria\n- Global developmental delay\n- Dystonia\n- Dysphagia\n- Infantile axial hypotonia\n- Abnormal circulating thyroid hormone concentration\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/00882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Spasticity\n- Dysarthria\n- Global developmental delay\n- Dystonia\n- Dysphagia\n- Infantile axial hypotonia\n- Abnormal circulating thyroid hormone concentration\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/00883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Spasticity\n- Dysarthria\n- Global developmental delay\n- Dystonia\n- Dysphagia\n- Infantile axial hypotonia\n- Abnormal circulating thyroid hormone concentration\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/00884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Spasticity\n- Dysarthria\n- Global developmental delay\n- Dystonia\n- Dysphagia\n- Infantile axial hypotonia\n- Abnormal circulating thyroid hormone concentration\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/00885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DPH5"}],"image":"exported_images\/00886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DPH5"}],"image":"exported_images\/00887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DPH5"}],"image":"exported_images\/00888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DPH5"}],"image":"exported_images\/00889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"THUMPD1"}],"image":"exported_images\/00890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"THUMPD1"}],"image":"exported_images\/00891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"THUMPD1"}],"image":"exported_images\/00892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"THUMPD1"}],"image":"exported_images\/00893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Keratitis\n- Uveitis\n- Delayed puberty\n- Eczema\n- Intellectual disability, mild\n- Failure to thrive\n- Recurrent skin infections\n- Pneumonia\n- Recurrent infections\n- Severe short stature\n- Severe recurrent varicella\n- Chronic pulmonary obstruction\n- Severe postnatal growth retardation\n- Severe varicella zoster infection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Growth hormone insensitivity syndrome with immune dysregulation"}],"image":"exported_images\/00894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of facial musculature\n- Ophthalmoparesis\n- Abnormality of the musculature of the upper limbs\n- Myopathy\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Short neck\n- Barrel-shaped chest\n- Abnormal lung morphology\n- Short stature\n- Recurrent pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Growth hormone insensitivity syndrome with immune dysregulation"}],"image":"exported_images\/00900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Upslanted palpebral fissure\n- Global developmental delay\n- Small for gestational age\n- Supernumerary nipple\n- Delayed skeletal maturation\n- Birth length less than 3rd percentile\n- Short stature\n- Decreased body weight\n- Proximal placement of thumb\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INSULIN-LIKE GROWTH FACTOR I DEFICIENCY"}],"image":"exported_images\/00901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Delayed puberty\n- Hashimoto thyroiditis\n- Eczema\n- Atopic dermatitis\n- Lethargy\n- Growth delay\n- Alopecia\n- Iron deficiency anemia\n- Constipation\n- Absent hair\n- Delayed skeletal maturation\n- Autoimmunity\n- Ichthyosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Growth hormone insensitivity syndrome with immune dysregulation"}],"image":"exported_images\/00902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Delayed puberty\n- Hashimoto thyroiditis\n- Eczema\n- Atopic dermatitis\n- Lethargy\n- Growth delay\n- Alopecia\n- Iron deficiency anemia\n- Constipation\n- Absent hair\n- Delayed skeletal maturation\n- Autoimmunity\n- Ichthyosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Growth hormone insensitivity syndrome with immune dysregulation"}],"image":"exported_images\/00903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Atopic dermatitis\n- Autoimmune thrombocytopenia\n- Abnormal lung morphology\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Abnormal subcutaneous fat tissue distribution\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARON SYNDROME"}],"image":"exported_images\/00904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Myotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myotonic dystrophy"}],"image":"exported_images\/00905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Scapular winging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/00907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VELOCARDIOFACIAL SYNDROME; VCFS"}],"image":"exported_images\/00908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 65; DEE65"}],"image":"exported_images\/00909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short neck\n- Strabismus\n- Hemangioma\n- Dandy-Walker malformation\n- Bilateral cryptorchidism\n- Dilatation of the renal pelvis\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"}],"image":"exported_images\/00910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAKER-GORDON SYNDROME; BAGOS"}],"image":"exported_images\/00911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Synophrys\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Dandy-Walker malformation\n- Poor motor coordination\n- Limb hypertonia\n- Highly arched eyebrow\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS"}],"image":"exported_images\/00912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Proteinuria\n- Microcephaly\n- Cholestasis\n- Failure to thrive\n- Hyperbilirubinemia\n- Distal arthrogryposis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, renal dysfunction, and cholestasis"}],"image":"exported_images\/00913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hydrocephalus\n- Iris coloboma\n- Optic atrophy\n- Anterior polar cataract\n- Seizure\n- Global developmental delay\n- Agenesis of corpus callosum\n- Cerebellar hypoplasia\n- EMG: myopathic abnormalities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Muscular dystrophy-dystroglycanopathy, type A"}],"image":"exported_images\/00914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hydrocephalus\n- Iris coloboma\n- Optic atrophy\n- Anterior polar cataract\n- Seizure\n- Global developmental delay\n- Agenesis of corpus callosum\n- Cerebellar hypoplasia\n- EMG: myopathic abnormalities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Muscular dystrophy-dystroglycanopathy, type A"}],"image":"exported_images\/00915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFAN SYNDROME; MFS"}],"image":"exported_images\/00916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Increased facial adipose tissue\n- Abnormal corpus callosum morphology\n- Cerebral atrophy\n- Progressive spasticity\n- Neurodevelopmental delay\n- Mildly reduced visual acuity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RADIO-TARTAGLIA SYNDROME; RATARS"}],"image":"exported_images\/00917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long palpebral fissure\n- Growth delay\n- Decreased body weight\n- Eversion of lateral third of lower eyelids\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypoplastic left heart syndrome"}],"image":"exported_images\/00918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Retrognathia\n- Low-set ears\n- Bulbous nose\n- Downslanted palpebral fissures\n- Ptosis\n- Exotropia\n- Pectus excavatum\n- Hypertension\n- Shield chest\n- Single transverse palmar crease\n- Muscle weakness\n- Cardiomyopathy\n- Left ventricular hypertrophy\n- Pes cavus\n- Talipes equinovarus\n- Low posterior hairline\n- Fused cervical vertebrae\n- Short stature\n- Absent phalangeal crease\n- Clinodactyly\n- Delayed ability to walk\n- Deviation of toes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Klippel-Feil syndrome"}],"image":"exported_images\/00919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High forehead\n- Anteverted nares\n- Telecanthus\n- Proptosis\n- Skin rash\n- Hypopigmentation of the skin\n- Brachydactyly\n- Failure to thrive\n- Talipes\n- Frontal bossing\n- Sparse scalp hair\n- Depressed nasal bridge\n- Sparse hair\n- Short distal phalanx of finger\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES; SSMCF"}],"image":"exported_images\/00920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Deeply set eye\n- Retinal dystrophy\n- Pigmentary retinopathy\n- Carious teeth\n- Jaundice\n- Cutaneous photosensitivity\n- Global developmental delay\n- Ascites\n- Ventriculomegaly\n- Hepatomegaly\n- Progressive neurologic deterioration\n- Elevated hepatic transaminase\n- Hypermethioninemia\n- Short stature\n- Decreased body weight\n- Prolonged prothrombin time\n- Postnatal growth retardation\n- Pedal edema\n- Periventricular white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME A; CSA"}],"image":"exported_images\/00921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sparse eyelashes\n- Hypohidrosis\n- Eczematoid dermatitis\n- Lymphedema\n- Hypopigmentation of the skin\n- Poikiloderma\n- Alopecia\n- Eosinophilia\n- Heat intolerance\n- Restrictive ventilatory defect\n- Pulmonary fibrosis\n- Alopecia of scalp\n- Myopathy\n- Skeletal muscle atrophy\n- Progressive muscle weakness\n- Lower-limb joint contracture\n- Fatty replacement of skeletal muscle\n- Sparse eyebrow\n- Telangiectasia of the skin\n- Cellulitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/00922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Macrotia\n- Aggressive behavior\n- Delayed speech and language development\n- Hypotonia\n- Mild short stature\n- Abnormality of dental morphology\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Intellectual disability, severe\n- Overhanging nasal tip\n- Delayed social development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72; MRT72"}],"image":"exported_images\/00923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Mandibular prognathia\n- Triangular nasal tip\n- Developmental cataract\n- Optic nerve hypoplasia\n- Delayed speech and language development\n- Delayed puberty\n- Seizure\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Cerebellar atrophy\n- Pes cavus\n- Limb ataxia\n- Intention tremor\n- Ventriculomegaly\n- Limb muscle weakness\n- Decreased body weight\n- Mild global developmental delay\n- Cerebellar hemisphere hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAREL-YOON SYNDROME; HAYOS"}],"image":"exported_images\/00924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Jaundice\n- Abnormality of the liver\n- Ascites\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Aortic valve stenosis\n- Prolonged QT interval\n- Splenomegaly\n- Overlapping toe\n- Respiratory distress\n- Generalized non-motor (absence) seizure\n- Polymicrogyria\n- Cortical irregularity\n- Unconjugated hyperbilirubinemia\n- Underdeveloped crus of the helix\n- Pulmonary insufficiency\n- Abnormality of the palmar creases\n- Long toe\n- Prominent forehead\n- Portal vein thrombosis\n- Abnormal diffusion weighted cerebral MRI morphology\n- Pulmonary edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY; CAFDADD"}],"image":"exported_images\/00925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Narrow forehead\n- Small forehead\n- Anteverted nares\n- Neonatal insulin-dependent diabetes mellitus\n- Platyspondyly\n- Osteopenia\n- Hirsutism\n- Lethargy\n- Cerebellar vermis hypoplasia\n- Weak cry\n- Deep philtrum\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Pneumonia\n- Cerebral cortical atrophy\n- Generalized myoclonic seizure\n- Increased serum lactate\n- Intracranial hemorrhage\n- Scoliosis\n- High, narrow palate\n- Thin bony cortex\n- Pathologic fracture\n- Kyphosis\n- Elevated hepatic transaminase\n- Hyperglycemia\n- Slender long bone\n- Mild short stature\n- Decreased body weight\n- Hypochromic microcytic anemia\n- Limited knee flexion\n- Bilateral cryptorchidism\n- Axial hypotonia\n- Simplified gyral pattern\n- Tented upper lip vermilion\n- EEG with burst suppression\n- Gastrostomy tube feeding in infancy\n- EEG with generalized polyspikes\n- Edema of the dorsum of feet\n- Infantile spasms\n- Moderate albuminuria\n- Profound global developmental delay\n- Clinodactyly\n- obsolete Small scrotum\n- Generalized myoclonic-tonic-clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, epilepsy, and diabetes syndrome"}],"image":"exported_images\/00926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Mandibular prognathia\n- Round face\n- Low-set ears\n- Visual impairment\n- Myopia\n- Aggressive behavior\n- Delayed speech and language development\n- Secondary amenorrhea\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Excessive daytime somnolence\n- Partial agenesis of the corpus callosum\n- Truncal obesity\n- Intellectual disability, moderate\n- Sleep disturbance\n- Poor speech\n- Downturned corners of mouth\n- Kyphoscoliosis\n- Depressed nasal bridge\n- Attention deficit hyperactivity disorder\n- Almond-shaped palpebral fissure\n- Hyperacusis\n- Severe global developmental delay\n- Flat face\n- Manifestations of perseverative thought or action\n- Maintenance insomnia\n- Decreased immunoglobulin level in body fluid\n- Lower limb asymmetry\n- Impulsivity\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB"}],"image":"exported_images\/00927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Hydronephrosis\n- High palate\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Hypermetropia\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Anteriorly placed anus\n- Oligohydramnios\n- Patent foramen ovale\n- Overlapping toe\n- Deep philtrum\n- Hypoplasia of the corpus callosum\n- Gait imbalance\n- Highly arched eyebrow\n- Recurrent infections\n- Renal malrotation\n- Depressed nasal bridge\n- Microtia\n- Axial hypotonia\n- Abnormal number of hair whorls\n- Feeding difficulties\n- Heart murmur\n- Arteria lusoria\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES; IDDILF"}],"image":"exported_images\/00928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Jaundice\n- Hypotonia\n- Choreoathetosis\n- Hyperreflexia\n- Hypothermia\n- Lower limb spasticity\n- Gait ataxia\n- Developmental regression\n- Axial hypotonia\n- Intellectual disability, severe\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 58; MRT58"}],"image":"exported_images\/00929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Low anterior hairline\n- Short philtrum\n- Narrow forehead\n- Thickened helices\n- Bulbous nose\n- Prominent nasal bridge\n- Deeply set eye\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Abnormal repetitive mannerisms\n- Reduced eye contact\n- Hypotonia\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Widely-spaced incisors\n- Developmental stagnation\n- Congenital blindness\n- EEG with focal epileptiform discharges\n- Hypoplasia of the pons\n- Thick vermilion border\n- Cerebral white matter atrophy\n- Overweight\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 23; DEE23"}],"image":"exported_images\/00930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Xerostomia\n- High palate\n- Narrow forehead\n- Ptosis\n- Upslanted palpebral fissure\n- Atypical behavior\n- Decreased response to growth hormone stimulation test\n- Dysarthria\n- Global developmental delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Growth delay\n- Intrauterine growth retardation\n- Hypernasal speech\n- Poor suck\n- Short nose\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Axial hypotonia\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22"}],"image":"exported_images\/00931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Xerostomia\n- High palate\n- Narrow forehead\n- Ptosis\n- Upslanted palpebral fissure\n- Atypical behavior\n- Decreased response to growth hormone stimulation test\n- Dysarthria\n- Global developmental delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Growth delay\n- Intrauterine growth retardation\n- Hypernasal speech\n- Poor suck\n- Short nose\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Axial hypotonia\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22"}],"image":"exported_images\/00932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Xerostomia\n- High palate\n- Narrow forehead\n- Ptosis\n- Upslanted palpebral fissure\n- Atypical behavior\n- Decreased response to growth hormone stimulation test\n- Dysarthria\n- Global developmental delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Growth delay\n- Intrauterine growth retardation\n- Hypernasal speech\n- Poor suck\n- Short nose\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Axial hypotonia\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 22; CMS22"}],"image":"exported_images\/00933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Broad forehead\n- Hearing impairment\n- Low-set ears\n- Cupped ear\n- Strabismus\n- Exotropia\n- Widely spaced teeth\n- Autism\n- Aggressive behavior\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Lethargy\n- Absent speech\n- Pulmonic stenosis\n- Patent foramen ovale\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Focal impaired awareness seizure\n- Short stature\n- Flat occiput\n- Focal-onset seizure\n- Feeding difficulties in infancy\n- Clonic seizure\n- Tonic seizure\n- Narrow palpebral fissure\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, 35; MRXS35"}],"image":"exported_images\/00934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUENKE SYNDROME; MNKES"}],"image":"exported_images\/00935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Hearing impairment\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Blue sclerae\n- Joint laxity\n- Umbilical hernia\n- Recurrent fractures\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Blepharocheilodontic syndrome"}],"image":"exported_images\/00936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Abnormality of the dentition\n- Gingival overgrowth\n- Thin vermilion border\n- Macrocephaly\n- Hypertelorism\n- Broad forehead\n- Low-set ears\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Brachydactyly\n- Mesomelia\n- External genital hypoplasia\n- Broad hallux\n- Bifid tongue\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Omodysplasia"}],"image":"exported_images\/00937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microretrognathia\n- Broad forehead\n- Narrow forehead\n- Hearing impairment\n- Optic disc pallor\n- Syndactyly\n- Hand polydactyly\n- Cerebellar hypoplasia\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Tetralogy of Fallot\n- Foot polydactyly\n- Ventriculomegaly\n- Short stature\n- Prominent nasal tip\n- CNS demyelination\n- Sparse hair\n- Prominent forehead\n- Severe global developmental delay\n- Overhanging nasal tip\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MAPKAPK5"}],"image":"exported_images\/00938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Pectus excavatum\n- Capitate-hamate fusion\n- Joint laxity\n- Short foot\n- Clinodactyly of the 5th toe\n- Genu recurvatum\n- Genu valgum\n- Hyperlordosis\n- Disproportionate short stature\n- Short palm\n- Multiple carpal ossification centers\n- Carpal synostosis\n- Short metacarpal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CATEL-MANZKE SYNDROME; CATMANS"}],"image":"exported_images\/00939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Abnormality of the ear\n- Osteopenia\n- Intellectual disability, mild\n- Global developmental delay\n- Hypernasal speech\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Ventriculomegaly\n- Aortic root aneurysm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/00940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin vermilion border\n- Smooth philtrum\n- Square face\n- Astigmatism\n- Ptosis\n- Myopia\n- Agenesis of corpus callosum\n- Gait disturbance\n- Gait ataxia\n- Contracture of the proximal interphalangeal joint of the 4th finger\n- Low hanging columella\n- Dyslexia\n- Intellectual disability, severe\n- Severe global developmental delay\n- Feeding difficulties\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 65; MRT65"}],"image":"exported_images\/00941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin vermilion border\n- Smooth philtrum\n- Square face\n- Astigmatism\n- Ptosis\n- Myopia\n- Agenesis of corpus callosum\n- Gait disturbance\n- Gait ataxia\n- Contracture of the proximal interphalangeal joint of the 4th finger\n- Low hanging columella\n- Dyslexia\n- Intellectual disability, severe\n- Severe global developmental delay\n- Feeding difficulties\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 65; MRT65"}],"image":"exported_images\/00942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Facial asymmetry\n- Broad forehead\n- Posteriorly rotated ears\n- Autistic behavior\n- Intellectual disability\n- Joint hypermobility\n- Large forehead\n- Finger joint hypermobility\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51"}],"image":"exported_images\/00943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Facial asymmetry\n- Broad forehead\n- Posteriorly rotated ears\n- Autistic behavior\n- Intellectual disability\n- Joint hypermobility\n- Large forehead\n- Finger joint hypermobility\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 51; MRD51"}],"image":"exported_images\/00944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Tall stature\n- Broad alveolar ridges\n- Thin upper lip vermilion\n- Macrocephaly\n- Malar flattening\n- Pointed chin\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Prominent supraorbital ridges\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Macrotia\n- Protruding ear\n- Wide nasal bridge\n- Depressed nasal tip\n- Broad nasal tip\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Hypermetropia\n- Long palpebral fissure\n- Ectropion\n- Widely spaced teeth\n- Dental malocclusion\n- Delayed speech and language development\n- Shield chest\n- Abnormal skull morphology\n- Abnormal posterior cranial fossa morphology\n- Thin skin\n- Hyperextensible skin\n- Large hands\n- Overgrowth\n- Long foot\n- Ventriculomegaly\n- Low posterior hairline\n- Exaggerated cupid's bow\n- Enlarged cisterna magna\n- Scoliosis\n- Abnormal calvaria morphology\n- Prominent frontal sinuses\n- Progressive flexion contractures\n- Focal white matter lesions\n- Hypoplasia of the frontal lobes\n- Prematurely aged appearance\n- Sparse hair\n- Infantile muscular hypotonia\n- Lipodystrophy\n- Prominent forehead\n- Camptodactyly\n- High insertion of columella\n- Wide nasal base\n- Long nasal bridge\n- Arachnoid cyst\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Tall stature\n- Broad alveolar ridges\n- Thin upper lip vermilion\n- Macrocephaly\n- Malar flattening\n- Pointed chin\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Prominent supraorbital ridges\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Macrotia\n- Protruding ear\n- Wide nasal bridge\n- Depressed nasal tip\n- Broad nasal tip\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Hypermetropia\n- Long palpebral fissure\n- Ectropion\n- Widely spaced teeth\n- Dental malocclusion\n- Delayed speech and language development\n- Shield chest\n- Abnormal skull morphology\n- Abnormal posterior cranial fossa morphology\n- Thin skin\n- Hyperextensible skin\n- Large hands\n- Overgrowth\n- Long foot\n- Ventriculomegaly\n- Low posterior hairline\n- Exaggerated cupid's bow\n- Enlarged cisterna magna\n- Scoliosis\n- Abnormal calvaria morphology\n- Prominent frontal sinuses\n- Progressive flexion contractures\n- Focal white matter lesions\n- Hypoplasia of the frontal lobes\n- Prematurely aged appearance\n- Sparse hair\n- Infantile muscular hypotonia\n- Lipodystrophy\n- Prominent forehead\n- Camptodactyly\n- High insertion of columella\n- Wide nasal base\n- Long nasal bridge\n- Arachnoid cyst\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Tall stature\n- Broad alveolar ridges\n- Thin upper lip vermilion\n- Macrocephaly\n- Malar flattening\n- Pointed chin\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Prominent supraorbital ridges\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Macrotia\n- Protruding ear\n- Wide nasal bridge\n- Depressed nasal tip\n- Broad nasal tip\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Hypermetropia\n- Long palpebral fissure\n- Ectropion\n- Widely spaced teeth\n- Dental malocclusion\n- Delayed speech and language development\n- Shield chest\n- Abnormal skull morphology\n- Abnormal posterior cranial fossa morphology\n- Thin skin\n- Hyperextensible skin\n- Large hands\n- Overgrowth\n- Long foot\n- Ventriculomegaly\n- Low posterior hairline\n- Exaggerated cupid's bow\n- Enlarged cisterna magna\n- Scoliosis\n- Abnormal calvaria morphology\n- Prominent frontal sinuses\n- Progressive flexion contractures\n- Focal white matter lesions\n- Hypoplasia of the frontal lobes\n- Prematurely aged appearance\n- Sparse hair\n- Infantile muscular hypotonia\n- Lipodystrophy\n- Prominent forehead\n- Camptodactyly\n- High insertion of columella\n- Wide nasal base\n- Long nasal bridge\n- Arachnoid cyst\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOSAKI OVERGROWTH SYNDROME; KOGS"}],"image":"exported_images\/00947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Myopia\n- Hypotonia\n- Motor delay\n- Agenesis of corpus callosum\n- Intellectual disability, moderate\n- Sleep disturbance\n- Hypoplastic left heart\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES; IDDHBA"}],"image":"exported_images\/00948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Micrognathia\n- Sensorineural hearing impairment\n- Optic disc coloboma\n- Dysarthria\n- Global developmental delay\n- Spastic tetraparesis\n- Cerebellar vermis hypoplasia\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Patent foramen ovale\n- Dysphagia\n- Gastroesophageal reflux\n- Unilateral microphthalmos\n- Delayed myelination\n- Anisometropia\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT ANOMALIES OF THE BRAIN, EYE, OR HEART; NEDBEH"}],"image":"exported_images\/00949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Intellectual disability, profound\n- Sleep disturbance\n- Secondary microcephaly\n- Generalized tonic seizure\n- Feeding difficulties\n- Delayed myelination\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, CATARACTS, FEEDING DIFFICULTIES, AND DELAYED BRAIN MYELINATION; NECFM"}],"image":"exported_images\/00950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Retrognathia\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Esotropia\n- Delayed speech and language development\n- Cerebellar atrophy\n- Corpus callosum atrophy\n- Axial hypotonia\n- Mild global developmental delay\n- Moderate global developmental delay\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR ATROPHY, VISUAL IMPAIRMENT, AND PSYCHOMOTOR RETARDATION; CAVIPMR"}],"image":"exported_images\/00951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Diabetes mellitus\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 48; MRD48"}],"image":"exported_images\/00952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin vermilion border\n- Large fontanelles\n- Microcephaly\n- Turricephaly\n- Coarse facial features\n- Mandibular prognathia\n- Broad forehead\n- Long philtrum\n- Telecanthus\n- Oligodontia\n- Delayed eruption of teeth\n- Thin skin\n- Cutis laxa\n- Prominent superficial veins\n- Brachydactyly\n- Absent speech\n- Joint laxity\n- Small for gestational age\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Kyphoscoliosis\n- Hip dislocation\n- Severe short stature\n- Decreased body weight\n- Diaphyseal thickening\n- Progeroid facial appearance\n- Excessive wrinkled skin\n- Sparse hair\n- Lipodystrophy\n- Small sella turcica\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin vermilion border\n- Large fontanelles\n- Microcephaly\n- Turricephaly\n- Coarse facial features\n- Mandibular prognathia\n- Broad forehead\n- Long philtrum\n- Telecanthus\n- Oligodontia\n- Delayed eruption of teeth\n- Thin skin\n- Cutis laxa\n- Prominent superficial veins\n- Brachydactyly\n- Absent speech\n- Joint laxity\n- Small for gestational age\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Kyphoscoliosis\n- Hip dislocation\n- Severe short stature\n- Decreased body weight\n- Diaphyseal thickening\n- Progeroid facial appearance\n- Excessive wrinkled skin\n- Sparse hair\n- Lipodystrophy\n- Small sella turcica\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LENZ-MAJEWSKI HYPEROSTOTIC DWARFISM; LMHD"}],"image":"exported_images\/00954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Prominent nasal bridge\n- Microphthalmia\n- Blepharophimosis\n- Global developmental delay\n- Cerebellar hypoplasia\n- Congenital hip dislocation\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Rocker bottom foot\n- Pneumonia\n- Respiratory failure\n- Premature closure of fontanelles\n- Distal arthrogryposis\n- Simplified gyral pattern\n- Flexion contracture of finger\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Warburg micro syndrome"}],"image":"exported_images\/00955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Abnormality of the ear\n- Autistic behavior\n- Delayed speech and language development\n- Delayed gross motor development\n- Language impairment\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Abnormality of the palpebral fissures\n- High anterior hairline\n- Thick nasal alae\n- Delayed fine motor development\n- Intellectual disability, severe\n- Narrow jaw\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF"}],"image":"exported_images\/00956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Hyporeflexia\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Cerebellar hypoplasia\n- Thoracolumbar scoliosis\n- CNS hypomyelination\n- Peripheral hypomyelination\n- Axial hypotonia\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KCTD3"}],"image":"exported_images\/00957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadism\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Overfolded helix\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Myopia\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Periorbital fullness\n- Long palpebral fissure\n- Optic atrophy\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Atrial septal defect\n- Toe syndactyly\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Generalized-onset seizure\n- Short stature\n- Persistent left superior vena cava\n- Intellectual disability, severe\n- Localized skin lesion\n- Flat face\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadism\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Overfolded helix\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Myopia\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Periorbital fullness\n- Long palpebral fissure\n- Optic atrophy\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Atrial septal defect\n- Toe syndactyly\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Generalized-onset seizure\n- Short stature\n- Persistent left superior vena cava\n- Intellectual disability, severe\n- Localized skin lesion\n- Flat face\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadism\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Overfolded helix\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Myopia\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Periorbital fullness\n- Long palpebral fissure\n- Optic atrophy\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Atrial septal defect\n- Toe syndactyly\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Generalized-onset seizure\n- Short stature\n- Persistent left superior vena cava\n- Intellectual disability, severe\n- Localized skin lesion\n- Flat face\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Skin creases, congenital symmetric circumferential"}],"image":"exported_images\/00960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micrognathia\n- Narrow nasal bridge\n- Proptosis\n- Shallow orbits\n- Hypertonia\n- Flexion contracture\n- Respiratory insufficiency\n- Ventriculomegaly\n- Scoliosis\n- High, narrow palate\n- Short stature\n- Decreased body weight\n- Recurrent pneumonia\n- Excessive wrinkled skin\n- Interictal epileptiform activity\n- Gastrostomy tube feeding in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEPPEN-LUBINSKY SYNDROME; KPLBS"}],"image":"exported_images\/00961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Large fontanelles\n- Turricephaly\n- Retrognathia\n- Hypertelorism\n- Triangular face\n- Abnormal pinna morphology\n- Downslanted palpebral fissures\n- Proptosis\n- Tooth malposition\n- Pectus excavatum\n- Platyspondyly\n- Motor delay\n- Small for gestational age\n- Oligohydramnios\n- Ventriculomegaly\n- Narrow iliac wing\n- Short stature\n- Reduced bone mineral density\n- Multiple prenatal fractures\n- Vertebral wedging\n- High iliac wing\n- Primary microcephaly\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cole-Carpenter syndrome"}],"image":"exported_images\/00962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Astigmatism\n- Downslanted palpebral fissures\n- Ataxia\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Abnormal heart morphology\n- Ventricular septal defect\n- Short stature\n- Decreased body weight\n- Rhizomelia\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, RHIZOMELIC, WITH MICROCEPHALY, MICROGNATHIA, AND DEVELOPMENTAL DELAY; SRMMD"}],"image":"exported_images\/00963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Trismus\n- High palate\n- Thin vermilion border\n- Full cheeks\n- Square face\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Strabismus\n- Telecanthus\n- Long eyelashes\n- Blepharophimosis\n- Autistic behavior\n- Rocker bottom foot\n- Short columella\n- Scoliosis\n- Kyphosis\n- Short nose\n- Clinodactyly of the 5th finger\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Gastrostomy tube feeding in infancy\n- Flat face\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CYSTIC FIBROSIS; CF"}],"image":"exported_images\/00964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Trismus\n- High palate\n- Thin vermilion border\n- Full cheeks\n- Square face\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Strabismus\n- Telecanthus\n- Long eyelashes\n- Blepharophimosis\n- Autistic behavior\n- Rocker bottom foot\n- Short columella\n- Scoliosis\n- Kyphosis\n- Short nose\n- Clinodactyly of the 5th finger\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Gastrostomy tube feeding in infancy\n- Flat face\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CYSTIC FIBROSIS; CF"}],"image":"exported_images\/00965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Trismus\n- High palate\n- Thin vermilion border\n- Full cheeks\n- Square face\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Strabismus\n- Telecanthus\n- Long eyelashes\n- Blepharophimosis\n- Autistic behavior\n- Rocker bottom foot\n- Short columella\n- Scoliosis\n- Kyphosis\n- Short nose\n- Clinodactyly of the 5th finger\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Gastrostomy tube feeding in infancy\n- Flat face\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CYSTIC FIBROSIS; CF"}],"image":"exported_images\/00966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Epicanthus\n- Facial hypotonia\n- Ptosis\n- Exotropia\n- Hypotonia\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Expressive language delay\n- Delayed fine motor development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 46; MRT46"}],"image":"exported_images\/00967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydronephrosis\n- Thin upper lip vermilion\n- Macrocephaly\n- High forehead\n- Delayed speech and language development\n- Intellectual disability\n- Agenesis of corpus callosum\n- Ventriculomegaly\n- Polymicrogyria\n- Interhemispheric cyst\n- Grade IV vesicoureteral reflux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRAIN MALFORMATIONS WITH OR WITHOUT URINARY TRACT DEFECTS; BRMUTD"}],"image":"exported_images\/00968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Proptosis\n- Failure to thrive\n- Splenomegaly\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Proptosis\n- Failure to thrive\n- Splenomegaly\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROLIDASE DEFICIENCY"}],"image":"exported_images\/00970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Intellectual disability, profound\n- Abnormal muscle tone\n- Intellectual disability, severe\n- Feeding difficulties\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES; NEDBAF"}],"image":"exported_images\/00971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypermetropia\n- Single transverse palmar crease\n- Tapered finger\n- Seizure\n- Hypotonia\n- Spasticity\n- Dystonia\n- Absent speech\n- Gait ataxia\n- Broad-based gait\n- Intellectual disability, profound\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH ATAXIC GAIT, ABSENT SPEECH, AND DECREASED CORTICAL WHITE MATTER; NDAGSCW"}],"image":"exported_images\/00972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Everted lower lip vermilion\n- Long face\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Delayed eruption of primary teeth\n- Narrow chest\n- Thin ribs\n- Short clavicles\n- Osteopenia\n- Syndactyly\n- Global developmental delay\n- Neonatal hypotonia\n- Ascites\n- Polyhydramnios\n- Patent foramen ovale\n- Wormian bones\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Decreased body weight\n- Depressed nasal bridge\n- 2-3 toe cutaneous syndactyly\n- Delayed pneumatization of the mastoid process\n- Airway obstruction\n- Periventricular heterotopia\n- Microtia\n- Overlapping fingers\n- Feeding difficulties\n- Camptodactyly\n- Irregular dentition\n- Hypoplasia of the olfactory bulb\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Van Maldergem syndrome"}],"image":"exported_images\/00973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Everted lower lip vermilion\n- Long face\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Delayed eruption of primary teeth\n- Narrow chest\n- Thin ribs\n- Short clavicles\n- Osteopenia\n- Syndactyly\n- Global developmental delay\n- Neonatal hypotonia\n- Ascites\n- Polyhydramnios\n- Patent foramen ovale\n- Wormian bones\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Decreased body weight\n- Depressed nasal bridge\n- 2-3 toe cutaneous syndactyly\n- Delayed pneumatization of the mastoid process\n- Airway obstruction\n- Periventricular heterotopia\n- Microtia\n- Overlapping fingers\n- Feeding difficulties\n- Camptodactyly\n- Irregular dentition\n- Hypoplasia of the olfactory bulb\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Van Maldergem syndrome"}],"image":"exported_images\/00974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Everted lower lip vermilion\n- Long face\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Delayed eruption of primary teeth\n- Narrow chest\n- Thin ribs\n- Short clavicles\n- Osteopenia\n- Syndactyly\n- Global developmental delay\n- Neonatal hypotonia\n- Ascites\n- Polyhydramnios\n- Patent foramen ovale\n- Wormian bones\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Decreased body weight\n- Depressed nasal bridge\n- 2-3 toe cutaneous syndactyly\n- Delayed pneumatization of the mastoid process\n- Airway obstruction\n- Periventricular heterotopia\n- Microtia\n- Overlapping fingers\n- Feeding difficulties\n- Camptodactyly\n- Irregular dentition\n- Hypoplasia of the olfactory bulb\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Van Maldergem syndrome"}],"image":"exported_images\/00975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Low-set ears\n- Strabismus\n- Visual impairment\n- Optic atrophy\n- Hypothyroidism\n- Hypotonia\n- Hepatosplenomegaly\n- Respiratory distress\n- Recurrent respiratory infections\n- Facial hypertrichosis\n- Inability to walk\n- Severe global developmental delay\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, FACIAL DYSMORPHISM, AND BRAIN ABNORMALITIES; NEDHFBA"}],"image":"exported_images\/00976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Pursed lips\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Adducted thumb\n- Ulnar deviation of the hand or of fingers of the hand\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Umbilical hernia\n- Talipes equinovarus\n- Calcaneovalgus deformity\n- Short columella\n- Gastroesophageal reflux\n- Respiratory insufficiency\n- Global brain atrophy\n- EEG abnormality\n- Scoliosis\n- Hip dislocation\n- Prominent nasolabial fold\n- Knee flexion contracture\n- Enlarged naris\n- Chin with H-shaped crease\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY; CLIFAHDD"}],"image":"exported_images\/00977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Retrognathia\n- Sensorineural hearing impairment\n- Convex nasal ridge\n- Hypermetropia\n- Microphthalmia\n- Hypotelorism\n- Hypothyroidism\n- Osteoporosis\n- Brachydactyly\n- Scoliosis\n- Long nose\n- Sparse hair\n- Narrow philtrum\n- Camptodactyly of finger\n- Lipoatrophy\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PREMATURE AGING SYNDROME, PENTTINEN TYPE; PENTT"}],"image":"exported_images\/00978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Macrotia\n- Downslanted palpebral fissures\n- Upper eyelid coloboma\n- Lower eyelid coloboma\n- Bilateral choanal atresia\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS, CINCINNATI TYPE; AFDCIN"}],"image":"exported_images\/00979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- Everted lower lip vermilion\n- Abnormal mastoid morphology\n- Abnormal mandible morphology\n- Abnormality of the orbital region\n- Hearing impairment\n- Cupped ear\n- Conductive hearing impairment\n- Sparse eyelashes\n- Alopecia\n- Short nose\n- Postauricular pit\n- Abnormal zygomatic arch morphology\n- Microtia\n- Congenital megaureter\n- Abnormality of the temporomandibular joint\n- Aplasia\/Hypoplasia of the eyelid\n- Abnormality of the sphenoid sinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA"}],"image":"exported_images\/00980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Delayed speech and language development\n- Hypertrichosis\n- Motor delay\n- Joint laxity\n- Talipes\n- Intellectual disability, moderate\n- Lumbar hyperlordosis\n- Depressed nasal bridge\n- Abdominal obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Delayed speech and language development\n- Hypertrichosis\n- Motor delay\n- Joint laxity\n- Talipes\n- Intellectual disability, moderate\n- Lumbar hyperlordosis\n- Depressed nasal bridge\n- Abdominal obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 58; MRD58"}],"image":"exported_images\/00982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Glossoptosis\n- Hypertelorism\n- Prominent supraorbital ridges\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Dysphagia\n- Broad thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE II; OPD2"}],"image":"exported_images\/00983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Anodontia\n- Hypohidrosis\n- Recurrent fever\n- Depressed nasal bridge\n- Sparse hair\n- Enlarged naris\n- Prominent forehead\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ectodermal dysplasia (select examples)"}],"image":"exported_images\/00984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Dilatation of the renal pelvis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Urofacial syndrome"}],"image":"exported_images\/00985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Short nose\n- Cranial hyperostosis\n- Hypoplasia of the primary teeth\n- Broad tibial metaphyses\n- Hyperostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniometaphyseal dysplasia"}],"image":"exported_images\/00986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAJDU-CHENEY SYNDROME; HJCYS"}],"image":"exported_images\/00987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Auriculocondylar syndrome"}],"image":"exported_images\/00988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VELOCARDIOFACIAL SYNDROME; VCFS"}],"image":"exported_images\/00989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COCKAYNE SYNDROME B; CSB"}],"image":"exported_images\/00990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHWARTZ-JAMPEL SYNDROME, TYPE 1; SJS1"}],"image":"exported_images\/00991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA; NEDIDHA"}],"image":"exported_images\/00992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA, INTELLECTUAL DISABILITY, NYSTAGMUS, AND OBESITY; SINO"}],"image":"exported_images\/00993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHITAYAT SYNDROME; CHYTS"}],"image":"exported_images\/00995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM, AND DYSMORPHIC FACIES; GDACCF"}],"image":"exported_images\/00996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, SEIZURES, AND ABSENT LANGUAGE; NDHSAL"}],"image":"exported_images\/00997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL\/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME; FHEIG"}],"image":"exported_images\/00998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL\/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME; FHEIG"}],"image":"exported_images\/00999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARTSOCAS-PAPAS SYNDROME 1; BPS1"}],"image":"exported_images\/01000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Ambiguous genitalia\n- Wide mouth\n- Low anterior hairline\n- Omphalocele\n- Clinodactyly of the 5th finger\n- Finger syndactyly\n- Microtia\n- Hypoplasia of eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ABLEPHARON-MACROSTOMIA SYNDROME; AMS"}],"image":"exported_images\/01001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION; NEDCPMD"}],"image":"exported_images\/01002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kenny-Caffey syndrome"}],"image":"exported_images\/01003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"APERT SYNDROME"}],"image":"exported_images\/01004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Acrodysostosis"}],"image":"exported_images\/01005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Anteverted nares\n- Strabismus\n- Narrow chest\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Spasticity\n- Motor delay\n- Talipes equinovarus\n- Achilles tendon contracture\n- Apnea\n- U-Shaped upper lip vermilion\n- Camptodactyly\n- Brain atrophy\n- Flexion contracture of finger\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis multiplex congenita"}],"image":"exported_images\/01006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KEIPERT SYNDROME; KPTS"}],"image":"exported_images\/01007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CSNK1G1"}],"image":"exported_images\/01008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Hypotonia\n- Global developmental delay\n- Joint hypermobility\n- Umbilical hernia\n- Bicuspid aortic valve\n- Coarse hair\n- Scoliosis\n- Thickened calvaria\n- High, narrow palate\n- Obstructive sleep apnea\n- Keloids\n- Hypoplasia of maxilla relative to mandible\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LATERAL MENINGOCELE SYNDROME; LMNS"}],"image":"exported_images\/01009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Oval face\n- Cafe-au-lait spot\n- Seizure\n- Spasticity\n- Global developmental delay\n- Motor delay\n- Hypertonia\n- Absent speech\n- Plagiocephaly\n- Polyhydramnios\n- Highly arched eyebrow\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Increased nuchal translucency\n- EEG with focal epileptiform discharges\n- Unilateral cryptorchidism\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES; NEDHYMS"}],"image":"exported_images\/01010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Epicanthus\n- Full cheeks\n- High forehead\n- Anteverted nares\n- Global developmental delay\n- Motor delay\n- Reduced tendon reflexes\n- Absent speech\n- Laryngomalacia\n- Frontal balding\n- Poor head control\n- 2-3 toe syndactyly\n- Flat occiput\n- 3-4 finger syndactyly\n- High anterior hairline\n- Medial flaring of the eyebrow\n- Abnormal helix morphology\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Infantile spasms\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION; NEDHRIT"}],"image":"exported_images\/01011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABAIS SA-DE VRIES SYNDROME, TYPE 1; NSDVS1"}],"image":"exported_images\/01012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS2"}],"image":"exported_images\/01013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, DYSTONIA, AND CEREBRAL HYPOMYELINATION; DDCH"}],"image":"exported_images\/01014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 76; DEE76"}],"image":"exported_images\/01015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCAF4"}],"image":"exported_images\/01016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS; BAIDCS"}],"image":"exported_images\/01017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LI-CAMPEAU SYNDROME; LICAS"}],"image":"exported_images\/01018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHANARIN-DORFMAN SYNDROME; CDS"}],"image":"exported_images\/01019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal tubular atrophy\n- Focal segmental glomerulosclerosis\n- Microcephaly\n- Prominent nose\n- Deeply set eye\n- Blepharitis\n- Hypermetropia\n- Nystagmus\n- Microdontia\n- Ataxia\n- Global developmental delay\n- Muscle weakness\n- Tremor\n- Freckling\n- Failure to thrive\n- Intrauterine growth retardation\n- Pancytopenia\n- Recurrent infections\n- Elevated circulating creatine kinase concentration\n- Short stature\n- Few cafe-au-lait spots\n- Bilateral sensorineural hearing impairment\n- Erythema\n- Nephrotic range proteinuria\n- Renal interstitial fibrosis\n- Renovascular hypertension\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fanconi anemia"}],"image":"exported_images\/01020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Hydronephrosis\n- Macrocephaly\n- Abnormality of the face\n- High forehead\n- Abnormality of the outer ear\n- Posteriorly rotated ears\n- Low-set ears\n- Abnormality of the eye\n- Strabismus\n- Coloboma\n- Atypical behavior\n- Delayed speech and language development\n- Precocious puberty\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Motor delay\n- Birth length less than 3rd percentile\n- Puberty and gonadal disorders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STANKIEWICZ-ISIDOR SYNDROME; STISS"}],"image":"exported_images\/01021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Palmoplantar keratoderma\n- Spontaneous, recurrent epistaxis\n- Elevated systolic blood pressure\n- Generalized ichthyosis\n- Elevated alkaline phosphatase of bone origin\n- Macroscopic hematuria\n- Mild proteinuria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, renal dysfunction, and cholestasis"}],"image":"exported_images\/01022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Velopharyngeal insufficiency\n- Full cheeks\n- Round face\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Ptosis\n- Long eyelashes\n- Delayed speech and language development\n- Hirsutism\n- Hypotonia\n- Laryngomalacia\n- Cardiomegaly\n- Dilated cardiomyopathy\n- Right ventricular hypertrophy\n- Left ventricular hypertrophy\n- Dysphagia\n- Delayed gross motor development\n- Scoliosis\n- Aspiration\n- Obstructive sleep apnea\n- Hip contracture\n- Short stature\n- Relative macrocephaly\n- Knee flexion contracture\n- Ankyloglossia\n- Delayed fine motor development\n- Gastrostomy tube feeding in infancy\n- Increased pulmonary capillary wedge pressure\n- Keratosis pilaris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiomyopathy, familial hypertrophic"}],"image":"exported_images\/01023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Abnormal facial shape\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53; MRD53"}],"image":"exported_images\/01024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Abnormal facial shape\n- Delayed gross motor development\n- Intellectual disability, severe\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 53; MRD53"}],"image":"exported_images\/01025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Growth abnormality\n- Abnormal facial shape\n- EEG abnormality\n- Intellectual disability, severe\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/01026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Growth abnormality\n- Abnormal facial shape\n- EEG abnormality\n- Intellectual disability, severe\n- Abnormal emotion\/affect behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 54; MRD54"}],"image":"exported_images\/01027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short chin\n- Narrow forehead\n- Long philtrum\n- Low-set ears\n- Protruding ear\n- Wide nasal bridge\n- Glaucoma\n- Long palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Fragile nails\n- Abnormal hallux morphology\n- Abnormal periventricular white matter morphology\n- Highly arched eyebrow\n- Short palm\n- Short stature\n- Flat forehead\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59"}],"image":"exported_images\/01028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short chin\n- Narrow forehead\n- Long philtrum\n- Low-set ears\n- Protruding ear\n- Wide nasal bridge\n- Glaucoma\n- Long palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Fragile nails\n- Abnormal hallux morphology\n- Abnormal periventricular white matter morphology\n- Highly arched eyebrow\n- Short palm\n- Short stature\n- Flat forehead\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 59; MRD59"}],"image":"exported_images\/01029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Abnormality of the dentition\n- High palate\n- Brachycephaly\n- Microcephaly\n- Coarse facial features\n- Hypertelorism\n- Otitis media\n- Astigmatism\n- Ptosis\n- Long eyelashes\n- Hypermetropia\n- Abnormality of the ear\n- Ectropion\n- Synophrys\n- Pectus excavatum\n- Narrow chest\n- Pruritus\n- Cholelithiasis\n- Hypotonia\n- Reduced tendon reflexes\n- Plagiocephaly\n- Hip dysplasia\n- Joint laxity\n- Abnormality of the liver\n- Hepatosplenomegaly\n- Polyhydramnios\n- Abnormal hair morphology\n- Premature birth\n- Patent ductus arteriosus\n- Bradycardia\n- Abnormal cardiac ventricle morphology\n- Exocrine pancreatic insufficiency\n- Short foot\n- Bilateral talipes equinovarus\n- Overlapping toe\n- Gastroesophageal reflux\n- Cerebral atrophy\n- EEG abnormality\n- Hypoplastic nipples\n- Steatorrhea\n- Downturned corners of mouth\n- Hip dislocation\n- Obstructive sleep apnea\n- Absent Achilles reflex\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Abnormality of bone mineral density\n- Abnormal nasal morphology\n- Distal arthrogryposis\n- Thick corpus callosum\n- Almond-shaped palpebral fissure\n- Fibular bowing\n- Central sleep apnea\n- Bilateral coxa valga\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Midface retrusion\n- Thoracic hypertrichosis\n- Increased serum bile acid concentration\n- Abnormal renal morphology\n- Thick vermilion border\n- Recurrent pancreatitis\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRICHOHEPATONEURODEVELOPMENTAL SYNDROME; THNS"}],"image":"exported_images\/01030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES; EDFAOB"}],"image":"exported_images\/01031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIZON-ISIDOR SYNDROME; NIZIDS"}],"image":"exported_images\/01032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES; NEDBAVC"}],"image":"exported_images\/01033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 13; DEE13"}],"image":"exported_images\/01034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MCCUNE-ALBRIGHT SYNDROME; MAS"}],"image":"exported_images\/01035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Hand tremor\n- Short stature\n- Echolalia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIN3B"}],"image":"exported_images\/01036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Tapered finger\n- Seizure\n- Generalized hypotonia\n- Intellectual disability, severe\n- Abnormal myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 50, AUTOSOMAL RECESSIVE; SPG50"}],"image":"exported_images\/01037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Soft skin\n- Hyperextensibility of the finger joints\n- Hypertonia\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cerebral creatine deficiency syndrome"}],"image":"exported_images\/01038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 34; MRXS34"}],"image":"exported_images\/01039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LEOPARD syndrome"}],"image":"exported_images\/01040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/01041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BIRK-BAREL SYNDROME; BIBARS"}],"image":"exported_images\/01042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARBACH-RUSTAD PROGEROID SYNDROME; MARUPS"}],"image":"exported_images\/01043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67; MRT67"}],"image":"exported_images\/01044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 26; SCA26"}],"image":"exported_images\/01045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE CONGENITAL ANOMALIES-NEURODEVELOPMENTAL SYNDROME, X-LINKED; MCAND"}],"image":"exported_images\/01046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFACIOSKELETAL SYNDROME WITH OR WITHOUT RENAL AGENESIS; NFSRA"}],"image":"exported_images\/01047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, ARMFIELD TYPE; MRXSA"}],"image":"exported_images\/01048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND\/OR STRUCTURAL BRAIN ABNORMALITIES; NEDASB"}],"image":"exported_images\/01049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS"}],"image":"exported_images\/01050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE; SDJLABA"}],"image":"exported_images\/01051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE; SDJLABA"}],"image":"exported_images\/01052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY; NEDESBA"}],"image":"exported_images\/01053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY; NEDBASS"}],"image":"exported_images\/01054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES; PAMDDFS"}],"image":"exported_images\/01055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES; NEDMABA"}],"image":"exported_images\/01056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES; NEDBAS"}],"image":"exported_images\/01057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED"}],"image":"exported_images\/01058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME; NEDJED"}],"image":"exported_images\/01059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS; NEDHAHM"}],"image":"exported_images\/01060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, SPONASTRIME TYPE; SEMDSP"}],"image":"exported_images\/01061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT; NEDSSWI"}],"image":"exported_images\/01062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARBACH-RUSTAD PROGEROID SYNDROME; MARUPS"}],"image":"exported_images\/01063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichothiodystrophy"}],"image":"exported_images\/01064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CULLER-JONES SYNDROME; CJS"}],"image":"exported_images\/01065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES; NDCAGF"}],"image":"exported_images\/01066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES; NDCAGF"}],"image":"exported_images\/01067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Smooth philtrum\n- Upslanted palpebral fissure\n- Oligodontia\n- Delayed puberty\n- Motor delay\n- Growth delay\n- Talipes equinovarus\n- Low hanging columella\n- Open bite\n- Motor regression\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, OLIGODONTIA, DYSMORPHIC FACIES, AND MOTOR DELAY; SOFM"}],"image":"exported_images\/01068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 5; MRT5"}],"image":"exported_images\/01069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial DNA depletion syndrome"}],"image":"exported_images\/01070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CARDIOSPONDYLOCARPOFACIAL SYNDROME; CSCF"}],"image":"exported_images\/01071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"STEEL SYNDROME; STLS"}],"image":"exported_images\/01072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 18; DEE18"}],"image":"exported_images\/01073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, LENS DISLOCATION, ANTERIOR SEGMENT ABNORMALITIES, AND SPONTANEOUS FILTERING BLEBS; FDLAB"}],"image":"exported_images\/01074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS; ABS1"}],"image":"exported_images\/01075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/01076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/01077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/01078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/01079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/01080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRANK-TER HAAR SYNDROME; FTHS"}],"image":"exported_images\/01081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, IMPAIRED INTELLECTUAL DEVELOPMENT, MICROCEPHALY, HYPOTONIA, AND OCULAR ANOMALIES; SIMHA"}],"image":"exported_images\/01082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DISABILITY-HYPOTONIC FACIES SYNDROME, X-LINKED, 1; MRXHF1"}],"image":"exported_images\/01083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GABRIELE-DE VRIES SYNDROME; GADEVS"}],"image":"exported_images\/01084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACS SYNDROME"}],"image":"exported_images\/01085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAM20B"}],"image":"exported_images\/01086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAM20B"}],"image":"exported_images\/01087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Triangular face\n- Low-set ears\n- Broad nasal tip\n- Deeply set eye\n- Myopia\n- Ventriculomegaly\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PAGANINI-MIOZZO SYNDROME; MRXSPM"}],"image":"exported_images\/01088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES; NEDMIBA"}],"image":"exported_images\/01089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULOSKELETODENTAL SYNDROME; OCSKD"}],"image":"exported_images\/01090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 39; MRT39"}],"image":"exported_images\/01091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY; GDRM"}],"image":"exported_images\/01092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SEIZURES, SCOLIOSIS, AND MACROCEPHALY\/MICROCEPHALY SYNDROME; SSMS"}],"image":"exported_images\/01093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS"}],"image":"exported_images\/01094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/01095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/01096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAFIQ SYNDROME; RAFQS"}],"image":"exported_images\/01097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE, FACIAL ANOMALIES, AND SPEECH DEFECTS; IDDSFAS"}],"image":"exported_images\/01098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YWHAZ"}],"image":"exported_images\/01099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FAUNDES-BANKA SYNDROME; FABAS"}],"image":"exported_images\/01100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19"}],"image":"exported_images\/01101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19"}],"image":"exported_images\/01102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SULEIMAN-EL-HATTAB SYNDROME; SULEHS"}],"image":"exported_images\/01103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Desbuquois dysplasia"}],"image":"exported_images\/01104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Preauricular skin tag\n- Thickened helices\n- Nystagmus\n- Brachydactyly\n- Seizure\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Deep philtrum\n- Highly arched eyebrow\n- Clinodactyly of the 5th finger\n- Short 4th metacarpal\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 95; DEE95"}],"image":"exported_images\/01105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 98; XLID98"}],"image":"exported_images\/01106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIX2"}],"image":"exported_images\/01107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR"}],"image":"exported_images\/01108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Otofaciocervical syndrome"}],"image":"exported_images\/01109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME; AAMR"}],"image":"exported_images\/01110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY-CAPILLARY MALFORMATION SYNDROME; MICCAP"}],"image":"exported_images\/01111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE; SPG47"}],"image":"exported_images\/01112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPINOCEREBELLAR ATAXIA 42, EARLY-ONSET, SEVERE, WITH NEURODEVELOPMENTAL DEFICITS; SCA42ND"}],"image":"exported_images\/01113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NANCE-HORAN SYNDROME; NHS"}],"image":"exported_images\/01114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facial paresis, hereditary congenital"}],"image":"exported_images\/01115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/01116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ELSAHY-WATERS SYNDROME; ESWS"}],"image":"exported_images\/01117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CORPUS CALLOSUM, AGENESIS OF, WITH FACIAL ANOMALIES AND ROBIN SEQUENCE"}],"image":"exported_images\/01118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Lissencephaly"}],"image":"exported_images\/01119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Central hypoventilation syndrome, congenital"}],"image":"exported_images\/01120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EMANUEL SYNDROME"}],"image":"exported_images\/01121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WARSAW BREAKAGE SYNDROME; WABS"}],"image":"exported_images\/01122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LACRIMOAURICULODENTODIGITAL SYNDROME; LADD"}],"image":"exported_images\/01123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES"}],"image":"exported_images\/01124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/01125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/01126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYOPATHY, CONGENITAL, BAILEY-BLOCH; MYPBB"}],"image":"exported_images\/01127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3"}],"image":"exported_images\/01128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B3; CMT4B3"}],"image":"exported_images\/01129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACTL6A"}],"image":"exported_images\/01130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 54; DEE54"}],"image":"exported_images\/01131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Renal hypoplasia\n- Abnormality of the ear\n- Global developmental delay\n- Tetralogy of Fallot\n- Absence of renal corticomedullary differentiation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT SYNDROME WITH OR WITHOUT HEARING LOSS, ABNORMAL EARS, OR DEVELOPMENTAL DELAY; CAKUTHED"}],"image":"exported_images\/01132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Infantile liver failure syndrome"}],"image":"exported_images\/01133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Epilepsy, progressive myoclonic"}],"image":"exported_images\/01134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF"}],"image":"exported_images\/01135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND DYSMORPHIC FACIES; NEDHYDF"}],"image":"exported_images\/01136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mandibuloacral dysplasia with lipodystrophy"}],"image":"exported_images\/01137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/01138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/01139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, STEREOTYPIC HAND MOVEMENTS, AND IMPAIRED LANGUAGE; NEDHSIL"}],"image":"exported_images\/01140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/01141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFANOID-PROGEROID-LIPODYSTROPHY SYNDROME; MFLS"}],"image":"exported_images\/01142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BARBER-SAY SYNDROME; BBRSAY"}],"image":"exported_images\/01143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, DYSMORPHIC FACIES, AND PSYCHOMOTOR RETARDATION; MDFPMR"}],"image":"exported_images\/01144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CURRARINO SYNDROME"}],"image":"exported_images\/01145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I; MOPD1"}],"image":"exported_images\/01146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I; MOPD1"}],"image":"exported_images\/01147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/01148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/01149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/01150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIABETES MELLITUS, NEONATAL, WITH CONGENITAL HYPOTHYROIDISM; NDH"}],"image":"exported_images\/01151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAGAMI-OGATA SYNDROME"}],"image":"exported_images\/01152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAGAMI-OGATA SYNDROME"}],"image":"exported_images\/01153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAGAMI-OGATA SYNDROME"}],"image":"exported_images\/01154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARFAN SYNDROME; MFS"}],"image":"exported_images\/01155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/01156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MELNICK-NEEDLES SYNDROME; MNS"}],"image":"exported_images\/01157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLYCINE ENCEPHALOPATHY WITH NORMAL SERUM GLYCINE"}],"image":"exported_images\/01158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 13; MRT13"}],"image":"exported_images\/01159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUJAN-FRYNS TYPE; MRXSLF"}],"image":"exported_images\/01160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUJAN-FRYNS TYPE; MRXSLF"}],"image":"exported_images\/01161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS-LIKE SYNDROME 1; PTHSL1"}],"image":"exported_images\/01162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Long philtrum\n- Low-set ears\n- Synophrys\n- Intellectual disability\n- Hypertonia\n- Proximal radio-ulnar synostosis\n- Short 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DDX23"}],"image":"exported_images\/01163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CK SYNDROME; CKS"}],"image":"exported_images\/01164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, X-LINKED; OHDOX"}],"image":"exported_images\/01165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial complex V (ATP synthase) deficiency, nuclear type"}],"image":"exported_images\/01166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mitochondrial complex V (ATP synthase) deficiency, nuclear type"}],"image":"exported_images\/01167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION; SSMED"}],"image":"exported_images\/01168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS; MIGSB"}],"image":"exported_images\/01169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TONNE-KALSCHEUER SYNDROME; TOKAS"}],"image":"exported_images\/01170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TONNE-KALSCHEUER SYNDROME; TOKAS"}],"image":"exported_images\/01171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PLXND1"}],"image":"exported_images\/01172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PLXND1"}],"image":"exported_images\/01173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"REV3L"}],"image":"exported_images\/01174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"REV3L"}],"image":"exported_images\/01175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DER WOUDE SYNDROME 1; VWS1"}],"image":"exported_images\/01176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 7; MRT7"}],"image":"exported_images\/01177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAKER-GORDON SYNDROME; BAGOS"}],"image":"exported_images\/01178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL MICROSOMIA; CFM"}],"image":"exported_images\/01179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JAWAD SYNDROME; JWDS"}],"image":"exported_images\/01180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Spasticity\n- Leukodystrophy\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/01181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Spasticity\n- Leukodystrophy\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALLAN-HERNDON-DUDLEY SYNDROME; AHDS"}],"image":"exported_images\/01182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/01183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/01184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/01185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME"}],"image":"exported_images\/01186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Abnormality of vision\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteopetrosis, autosomal recessive"}],"image":"exported_images\/01187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB-SHAFFER SYNDROME; LAMSHF"}],"image":"exported_images\/01188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBINOW-SORAUF SYNDROME"}],"image":"exported_images\/01189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SWEENEY-COX SYNDROME; SWCOS"}],"image":"exported_images\/01190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DUANE-RADIAL RAY SYNDROME; DRRS"}],"image":"exported_images\/01191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Aggressive behavior\n- Compulsive behaviors\n- Abnormal thumb morphology\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Metatarsus adductus\n- Gait ataxia\n- Ventriculomegaly\n- Delayed gross motor development\n- Elbow flexion contracture\n- Inverted nipples\n- Ankyloglossia\n- Malar prominence\n- Receptive language delay\n- Delayed myelination\n- T2 hypointense basal ganglia\n- Abnormal hippocampus morphology\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70"}],"image":"exported_images\/01192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Aggressive behavior\n- Compulsive behaviors\n- Abnormal thumb morphology\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Metatarsus adductus\n- Gait ataxia\n- Ventriculomegaly\n- Delayed gross motor development\n- Elbow flexion contracture\n- Inverted nipples\n- Ankyloglossia\n- Malar prominence\n- Receptive language delay\n- Delayed myelination\n- T2 hypointense basal ganglia\n- Abnormal hippocampus morphology\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70"}],"image":"exported_images\/01193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Aggressive behavior\n- Compulsive behaviors\n- Abnormal thumb morphology\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Metatarsus adductus\n- Gait ataxia\n- Ventriculomegaly\n- Delayed gross motor development\n- Elbow flexion contracture\n- Inverted nipples\n- Ankyloglossia\n- Malar prominence\n- Receptive language delay\n- Delayed myelination\n- T2 hypointense basal ganglia\n- Abnormal hippocampus morphology\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70"}],"image":"exported_images\/01194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Aggressive behavior\n- Compulsive behaviors\n- Abnormal thumb morphology\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Metatarsus adductus\n- Gait ataxia\n- Ventriculomegaly\n- Delayed gross motor development\n- Elbow flexion contracture\n- Inverted nipples\n- Ankyloglossia\n- Malar prominence\n- Receptive language delay\n- Delayed myelination\n- T2 hypointense basal ganglia\n- Abnormal hippocampus morphology\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70"}],"image":"exported_images\/01195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Aggressive behavior\n- Compulsive behaviors\n- Abnormal thumb morphology\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Metatarsus adductus\n- Gait ataxia\n- Ventriculomegaly\n- Delayed gross motor development\n- Elbow flexion contracture\n- Inverted nipples\n- Ankyloglossia\n- Malar prominence\n- Receptive language delay\n- Delayed myelination\n- T2 hypointense basal ganglia\n- Abnormal hippocampus morphology\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 70; DEE70"}],"image":"exported_images\/01196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOXA2"}],"image":"exported_images\/01197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 38; MRD38"}],"image":"exported_images\/01198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 38; MRD38"}],"image":"exported_images\/01199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES; IDDBCS"}],"image":"exported_images\/01200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES; IDDBCS"}],"image":"exported_images\/01201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE; MRXSCH"}],"image":"exported_images\/01202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PROTEUS SYNDROME"}],"image":"exported_images\/01203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFACIAL DYSMORPHISM, SKELETAL ANOMALIES, AND MENTAL RETARDATION SYNDROME; CFSMR"}],"image":"exported_images\/01204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Focal facial dermal dysplasia"}],"image":"exported_images\/01205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, ONYCHODYSTROPHY, OSTEODYSTROPHY, MENTAL RETARDATION, AND SEIZURES SYNDROME; DOORS"}],"image":"exported_images\/01206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SALT AND PEPPER DEVELOPMENTAL REGRESSION SYNDROME; SPDRS"}],"image":"exported_images\/01207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRIAS SYNDROME"}],"image":"exported_images\/01208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS"}],"image":"exported_images\/01209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETTIGREW SYNDROME; PGS"}],"image":"exported_images\/01210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DEN ENDE-GUPTA SYNDROME; VDEGS"}],"image":"exported_images\/01211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VAN DEN ENDE-GUPTA SYNDROME; VDEGS"}],"image":"exported_images\/01212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Neu-Laxova syndrome"}],"image":"exported_images\/01213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PETERS-PLUS SYNDROME; PTRPLS"}],"image":"exported_images\/01214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FILIPPI SYNDROME; FLPIS"}],"image":"exported_images\/01215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHPRINTZEN-GOLDBERG CRANIOSYNOSTOSIS SYNDROME; SGS"}],"image":"exported_images\/01216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPOTONIA, SEIZURES, AND CEREBELLAR ATROPHY; NEDHSCA"}],"image":"exported_images\/01217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Platyspondyly\n- Brachydactyly\n- Kyphoscoliosis\n- Disproportionate short-trunk short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spondylometaphyseal dysplasia"}],"image":"exported_images\/01218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ATP9A"}],"image":"exported_images\/01219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Global developmental delay\n- Cerebellar hypoplasia\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES"}],"image":"exported_images\/01220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Short toe\n- Fibular hypoplasia\n- obsolete Radially deviated index finger phalanges\n- Short finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Acromesomelic dysplasia"}],"image":"exported_images\/01221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dolichocephaly\n- Malar flattening\n- Long eyelashes\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Slender finger\n- Global developmental delay\n- Highly arched eyebrow\n- Scoliosis\n- 4-5 toe syndactyly\n- Brittle scalp hair\n- Increased laxity of fingers\n- Staring gaze\n- Clinodactyly of the 3rd finger\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LAMB4"}],"image":"exported_images\/01222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 84; DEE84"}],"image":"exported_images\/01223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Macrocephaly\n- Myopia\n- Atypical behavior\n- Intellectual disability, mild\n- Obesity\n- Talipes valgus\n- Attention deficit hyperactivity disorder\n- Enuresis nocturna\n- Abnormal eating behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JARID2"}],"image":"exported_images\/01224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Hydrocephalus\n- Adducted thumb\n- Intellectual disability\n- Spastic tetraparesis\n- Pes planus\n- Aqueductal stenosis\n- Anarthria\n- Bowel incontinence\n- Thoracolumbar scoliosis\n- Talipes valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spastic paraplegia"}],"image":"exported_images\/01225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT EARLY-ONSET GENERALIZED EPILEPSY; NEDEGE"}],"image":"exported_images\/01226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Developmental stagnation at onset of seizures\n- Multifocal epileptiform discharges\n- Epileptic encephalopathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 7; DEE7"}],"image":"exported_images\/01227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME; POBINDS"}],"image":"exported_images\/01228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Deeply set eye\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Small for gestational age\n- Ventriculomegaly\n- Delayed gross motor development\n- Exaggerated cupid's bow\n- Difficulty walking\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Glut1 deficiency syndrome"}],"image":"exported_images\/01229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Deeply set eye\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Small for gestational age\n- Ventriculomegaly\n- Delayed gross motor development\n- Exaggerated cupid's bow\n- Difficulty walking\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Glut1 deficiency syndrome"}],"image":"exported_images\/01230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Deeply set eye\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Small for gestational age\n- Ventriculomegaly\n- Delayed gross motor development\n- Exaggerated cupid's bow\n- Difficulty walking\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Glut1 deficiency syndrome"}],"image":"exported_images\/01231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Global developmental delay\n- Motor delay\n- Delayed gross motor development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Usher syndrome"}],"image":"exported_images\/01232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Generalized-onset seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY; IDDMSSD"}],"image":"exported_images\/01233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autistic behavior\n- Global developmental delay\n- Obesity\n- Cutaneous mastocytosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLOBAL DEVELOPMENTAL DELAY WITH SPEECH AND BEHAVIORAL ABNORMALITIES; GDSBA"}],"image":"exported_images\/01234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Brachycephaly\n- Delayed speech and language development\n- Motor delay\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR DYSFUNCTION WITH VARIABLE COGNITIVE AND BEHAVIORAL ABNORMALITIES; CECBA"}],"image":"exported_images\/01235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal insufficiency\n- Congestive heart failure\n- Dehydration\n- Respiratory failure\n- Abnormality of vitamin B12 metabolism\n- Disseminated intravascular coagulation\n- Intraventricular hemorrhage\n- Neonatal seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Methylmalonic aciduria and homocystinuria"}],"image":"exported_images\/01236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sparse eyelashes\n- Hypohidrosis\n- Eczematoid dermatitis\n- Lymphedema\n- Hypopigmentation of the skin\n- Poikiloderma\n- Alopecia\n- Eosinophilia\n- Heat intolerance\n- Restrictive ventilatory defect\n- Pulmonary fibrosis\n- Alopecia of scalp\n- Myopathy\n- Skeletal muscle atrophy\n- Progressive muscle weakness\n- Lower-limb joint contracture\n- Fatty replacement of skeletal muscle\n- Sparse eyebrow\n- Telangiectasia of the skin\n- Cellulitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY, AND PULMONARY FIBROSIS; POIKTMP"}],"image":"exported_images\/01237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Conjunctival telangiectasia\n- Nystagmus\n- Ataxia\n- Cerebellar atrophy\n- Gait disturbance\n- Slurred speech\n- Intention tremor\n- Broad-based gait\n- Gait imbalance\n- Recurrent respiratory infections\n- Frequent falls\n- Elevated circulating alpha-fetoprotein concentration\n- Limb tremor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ATAXIA-TELANGIECTASIA; AT"}],"image":"exported_images\/01238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High palate\n- Retrognathia\n- Short philtrum\n- Sloping forehead\n- Underdeveloped nasal alae\n- Prominent nose\n- Anxiety\n- Slender finger\n- Motor delay\n- Clinodactyly of the 5th toe\n- Recurrent respiratory infections\n- Drooling\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Long nose\n- Hyperlordosis\n- obsolete Large beaked nose\n- Prominent nasal septum\n- Clinodactyly of the 3rd toe\n- Hyperextensibility at elbow\n- Increased overbite\n- Darwin tubercle of helix\n- Clinodactyly of the 4th toe\n- Premature adrenarche\n- Emotional hypersensitivity\n- Thick hair\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAF4"}],"image":"exported_images\/01239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Microcephaly\n- Long face\n- Short philtrum\n- Narrow forehead\n- Prominent nasal bridge\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Macrodontia of permanent maxillary central incisor\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- High, narrow palate\n- Horizontal pendular nystagmus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI-YUAN SYNDROME; ALYUS"}],"image":"exported_images\/01240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ASPARAGINE SYNTHETASE DEFICIENCY; ASNSD"}],"image":"exported_images\/01241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUENKE SYNDROME; MNKES"}],"image":"exported_images\/01242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASAL CELL NEVUS SYNDROME; BCNS"}],"image":"exported_images\/01243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 1p36 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/01244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- High palate\n- Bulbous nose\n- Anteverted nares\n- Upslanted palpebral fissure\n- Aggressive behavior\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Polyhydramnios\n- Short foot\n- Hydrops fetalis\n- Broad toe\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Low posterior hairline\n- Intellectual disability, moderate\n- Scoliosis\n- Short palm\n- Large earlobe\n- Frequent temper tantrums\n- Overweight\n- Preeclampsia\n- Cyanotic episode\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/01245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- High palate\n- Bulbous nose\n- Anteverted nares\n- Upslanted palpebral fissure\n- Aggressive behavior\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Polyhydramnios\n- Short foot\n- Hydrops fetalis\n- Broad toe\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Low posterior hairline\n- Intellectual disability, moderate\n- Scoliosis\n- Short palm\n- Large earlobe\n- Frequent temper tantrums\n- Overweight\n- Preeclampsia\n- Cyanotic episode\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/01246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- High palate\n- Bulbous nose\n- Anteverted nares\n- Upslanted palpebral fissure\n- Aggressive behavior\n- Tapered finger\n- Global developmental delay\n- Neonatal hypotonia\n- Polyhydramnios\n- Short foot\n- Hydrops fetalis\n- Broad toe\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Low posterior hairline\n- Intellectual disability, moderate\n- Scoliosis\n- Short palm\n- Large earlobe\n- Frequent temper tantrums\n- Overweight\n- Preeclampsia\n- Cyanotic episode\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 94; DEE94"}],"image":"exported_images\/01247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/01248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"EPILEPSY, FOCAL, WITH SPEECH DISORDER AND WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT; FESD"}],"image":"exported_images\/01249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Broad forehead\n- Convex nasal ridge\n- Strabismus\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Brisk reflexes\n- Kyphoscoliosis\n- Short stature\n- Microtia\n- Clinodactyly\n- Weakness of facial musculature\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHUKLA-VERNON SYNDROME; SHUVER"}],"image":"exported_images\/01250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Abnormality of the ear\n- Osteopenia\n- Intellectual disability, mild\n- Global developmental delay\n- Hypernasal speech\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Ventriculomegaly\n- Aortic root aneurysm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIFRIM-HITZ-WEISS SYNDROME; SIHIWES"}],"image":"exported_images\/01251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of head or neck\n- Abnormality of the nervous system\n- Abnormality of prenatal development or birth\n- Global developmental delay\n- Abnormality of the integument\n- Abnormality of the cardiovascular system\n- Abnormality of limbs\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA; CHDED"}],"image":"exported_images\/01252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GOMEZ-LOPEZ-HERNANDEZ SYNDROME; GLHS"}],"image":"exported_images\/01253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 65; DEE65"}],"image":"exported_images\/01254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRUNET-WAGNER NEURODEVELOPMENTAL SYNDROME; BRUWAG"}],"image":"exported_images\/01255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Abnormality of the ear\n- Autistic behavior\n- Delayed speech and language development\n- Delayed gross motor development\n- Language impairment\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Abnormality of the palpebral fissures\n- High anterior hairline\n- Thick nasal alae\n- Delayed fine motor development\n- Intellectual disability, severe\n- Narrow jaw\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPERTELORISM AND DISTINCTIVE FACIES; IDDHDF"}],"image":"exported_images\/01256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DONNAI-BARROW SYNDROME"}],"image":"exported_images\/01257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 2q37 DELETION SYNDROME"}],"image":"exported_images\/01258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH SHORT STATURE, DYSMORPHIC FACIAL FEATURES, AND SPARSE HAIR; DEDSSH"}],"image":"exported_images\/01259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Muscular dystrophy-dystroglycanopathy, type A"}],"image":"exported_images\/01260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, BRACHYDACTYLY, IMPAIRED INTELLECTUAL DEVELOPMENT, AND SEIZURES; SBIDDS"}],"image":"exported_images\/01261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CIMDAG SYNDROME; CIMDAG"}],"image":"exported_images\/01262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CIMDAG SYNDROME; CIMDAG"}],"image":"exported_images\/01263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Malar flattening\n- Prominent supraorbital ridges\n- Hearing impairment\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Osteopenia\n- Limitation of joint mobility\n- Joint laxity\n- Barrel-shaped chest\n- Laryngomalacia\n- Congestive heart failure\n- Cardiomyopathy\n- Short foot\n- Frontal bossing\n- Scoliosis\n- Platybasia\n- Obstructive sleep apnea\n- Lumbar hyperlordosis\n- Tibial bowing\n- Elbow flexion contracture\n- Mesomelia\n- Hypoplasia of the capital femoral epiphysis\n- Short stature\n- Biconcave vertebral bodies\n- Restricted large joint movement\n- Limited shoulder movement\n- Recurrent pneumonia\n- Aplasia\/Hypoplasia of the tarsal bones\n- Benign prostatic hyperplasia\n- Hypoplasia of the femoral head\n- Short metacarpal\n- Fibular bowing\n- Facial palsy\n- Small proximal tibial epiphyses\n- Wide nasal base\n- Clinodactyly\n- Short femoral neck\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spondyloepimetaphyseal dysplasia with joint laxity"}],"image":"exported_images\/01264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Large hands\n- Intellectual disability, mild\n- S-shaped palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN-GIBSON SYNDROME; COGIS"}],"image":"exported_images\/01265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Growth delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RADIO-TARTAGLIA SYNDROME; RATARS"}],"image":"exported_images\/01266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Low-set ears\n- Atresia of the external auditory canal\n- Sacral dimple\n- Hypertrichosis\n- Single umbilical artery\n- Hypotonia\n- Motor delay\n- Growth delay\n- Polyhydramnios\n- Coarctation of aorta\n- Anemia\n- Ventriculomegaly\n- Ileus\n- Recurrent infections\n- Respiratory failure\n- Short long bone\n- Elevated circulating creatinine concentration\n- Feeding difficulties in infancy\n- Overlapping fingers\n- Concave nasal ridge\n- Nasogastric tube feeding in infancy\n- Feeding difficulties\n- Dorsocervical fat pad\n- Livedo reticularis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEGCAGS SYNDROME; DEGCAGS"}],"image":"exported_images\/01267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Downslanted palpebral fissures\n- Periorbital fullness\n- Delayed speech and language development\n- Sparse scalp hair\n- Deep palmar crease\n- Excessive wrinkled skin\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WRINKLY SKIN SYNDROME; WSS"}],"image":"exported_images\/01268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- Everted lower lip vermilion\n- Abnormal mastoid morphology\n- Abnormal mandible morphology\n- Abnormality of the orbital region\n- Hearing impairment\n- Cupped ear\n- Conductive hearing impairment\n- Sparse eyelashes\n- Alopecia\n- Short nose\n- Postauricular pit\n- Abnormal zygomatic arch morphology\n- Microtia\n- Congenital megaureter\n- Abnormality of the temporomandibular joint\n- Aplasia\/Hypoplasia of the eyelid\n- Abnormality of the sphenoid sinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS WITH ALOPECIA; MFDA"}],"image":"exported_images\/01269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Spondyloepiphyseal dysplasia\n- Genu varum\n- Acetabular dysplasia\n- Disproportionate short-limb short stature\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE; SEMDIST"}],"image":"exported_images\/01270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Seizure\n- Global developmental delay\n- Muscle weakness\n- Generalized hypopigmentation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Griscelli syndrome"}],"image":"exported_images\/01271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH, DYSMORPHIC FACIES, AND VARIABLE SKELETAL ANOMALIES; IDNADFS"}],"image":"exported_images\/01272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Hypogonadotropic hypogonadism\n- Wide mouth\n- Macroglossia\n- Facial hypotonia\n- Strabismus\n- Widely spaced teeth\n- Delayed speech and language development\n- Delayed puberty\n- Intellectual disability\n- Seizure\n- Spasticity\n- Global developmental delay\n- Spastic diplegia\n- Motor delay\n- Hypertonia\n- Overlapping toe\n- Dysphagia\n- Gastroesophageal reflux\n- Gait ataxia\n- EEG abnormality\n- Scoliosis\n- Short stature\n- Hypochromic microcytic anemia\n- EEG with spike-wave complexes (<2.5 Hz)\n- Prominent forehead\n- Central hypothyroidism\n- EEG with generalized polyspikes\n- Thick vermilion border\n- Abnormal growth hormone level\n- Cerebral palsy\n- Barrett esophagus\n- EEG with frontal epileptiform discharges\n- EEG with occipital epileptiform discharges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PPFIA3"}],"image":"exported_images\/01273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Diamond-Blackfan anemia"}],"image":"exported_images\/01274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Delayed cranial suture closure\n- Long philtrum\n- Downslanted palpebral fissures\n- Cutis laxa\n- Short nose\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Congenital disorders of glycosylation, type II"}],"image":"exported_images\/01281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Spondyloepiphyseal dysplasia\n- Disproportionate short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SPONDYLOEPIPHYSEAL DYSPLASIA CONGENITA; SEDC"}],"image":"exported_images\/01282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C3"}],"image":"exported_images\/01283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C9"}],"image":"exported_images\/01284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Disproportionate short stature\n- Rhizomelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACHONDROPLASIA; ACH"}],"image":"exported_images\/01285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Hypertelorism\n- Broad forehead\n- Stenosis of the external auditory canal\n- Failure to thrive\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 18q DELETION SYNDROME"}],"image":"exported_images\/01286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RECQL"}],"image":"exported_images\/01287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TRPM3"}],"image":"exported_images\/01288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NAE1"}],"image":"exported_images\/01289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PGM2L1"}],"image":"exported_images\/01290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PGM2L1"}],"image":"exported_images\/01291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/01292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARPC4"}],"image":"exported_images\/01293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRA10AC1"}],"image":"exported_images\/01294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZSCAN10"}],"image":"exported_images\/01295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Specific learning disability\n- Obesity\n- Decreased circulating IgA level\n- Recurrent upper respiratory tract infections\n- Decreased circulating IgG level\n- Elevated circulating alpha-fetoprotein concentration\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RIDDLE SYNDROME; RIDL"}],"image":"exported_images\/01296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Specific learning disability\n- Obesity\n- Decreased circulating IgA level\n- Recurrent upper respiratory tract infections\n- Decreased circulating IgG level\n- Elevated circulating alpha-fetoprotein concentration\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RIDDLE SYNDROME; RIDL"}],"image":"exported_images\/01297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Malar flattening\n- Small face\n- Epicanthus\n- Bird-like facies\n- Sloping forehead\n- Long philtrum\n- Micrognathia\n- Abnormality of the outer ear\n- Low-set, posteriorly rotated ears\n- Prominent nasal bridge\n- Downslanted palpebral fissures\n- Abnormality of the skin\n- Global developmental delay\n- Growth delay\n- Thrombocytopenia\n- Pancytopenia\n- Lymphopenia\n- Recurrent infections\n- Immunodeficiency\n- Decreased circulating total IgM\n- Increased circulating IgA level\n- Abnormal bone structure\n- Decreased circulating IgG level\n- Short stature\n- Low hanging columella\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL DYSMORPHISM, IMMUNODEFICIENCY, LIVEDO, AND SHORT STATURE; FILS"}],"image":"exported_images\/01298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypopigmented skin patches\n- Subependymal cysts\n- Renal cell carcinoma\n- Renal angiomyolipoma\n- Shagreen patch\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Tuberous sclerosis"}],"image":"exported_images\/01299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Micrognathia\n- Natal tooth\n- Small for gestational age\n- Atrial septal defect\n- Neutropenia\n- Lymphopenia\n- Anemia\n- Respiratory distress\n- Intestinal malrotation\n- Downturned corners of mouth\n- Decreased circulating IgA level\n- Limb undergrowth\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMMUNODEFICIENCY 23; IMD23"}],"image":"exported_images\/01300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DPH5"}],"image":"exported_images\/01301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"THUMPD1"}],"image":"exported_images\/01302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Muscle weakness\n- Myotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myotonic dystrophy"}],"image":"exported_images\/01303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed puberty\n- Eczema\n- Failure to thrive\n- Growth delay\n- Intrauterine growth retardation\n- Chronic diarrhea\n- Respiratory insufficiency\n- Steatorrhea\n- Severe short stature\n- Severe recurrent varicella\n- Chronic lung disease\n- Whooping cough\n- Severe varicella zoster infection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Growth hormone insensitivity syndrome with immune dysregulation"}],"image":"exported_images\/01304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Myopathic facies\n- Severe muscular hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Myopathy, centronuclear"}],"image":"exported_images\/01305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Short upper lip\n- Triangular mouth\n- Hypertelorism\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Delayed eruption of permanent teeth\n- Joint hypermobility\n- Hip dysplasia\n- Protuberant abdomen\n- Talipes equinovarus\n- Pes planus\n- Sandal gap\n- Short stature\n- Decreased body weight\n- Short finger\n- Proximal placement of thumb\n- Medial flaring of the eyebrow\n- Broad thumb\n- Clinodactyly\n- Decreased serum insulin-like growth factor 1\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INSULIN-LIKE GROWTH FACTOR I DEFICIENCY"}],"image":"exported_images\/01306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Atopic dermatitis\n- Abnormal lung morphology\n- Delayed skeletal maturation\n- Severe short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Abnormal subcutaneous fat tissue distribution\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARON SYNDROME"}],"image":"exported_images\/01307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Facioscapulohumeral muscular dystrophy"}],"image":"exported_images\/01308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Long philtrum\n- Abnormal nasal tip morphology\n- Periorbital fullness\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Widely spaced teeth\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Prominent nose\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Intellectual disability\n- Coma\n- Meningitis\n- Delayed gross motor development\n- Short stature\n- Decreased body weight\n- Prominent nasolabial fold\n- Deep palmar crease\n- Hyperacusis\n- Everted upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Periorbital fullness\n- Specific learning disability\n- Small for gestational age\n- Clinodactyly of the 5th finger\n- Short stature\n- Supravalvular aortic stenosis\n- Lower limb hypertonia\n- Stellate iris\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Motor delay\n- Growth delay\n- Pulmonic stenosis\n- Hypercalcemia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Long philtrum\n- Broad nasal tip\n- Periorbital fullness\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Long philtrum\n- Broad nasal tip\n- Periorbital fullness\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Abnormality of the philtrum\n- Short chin\n- Anteverted nares\n- Periorbital fullness\n- Abnormal cheek morphology\n- Prominent nasolabial fold\n- Abnormal shape of the frontal region\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Short chin\n- Bulbous nose\n- Long neck\n- Periorbital fullness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Facial asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormal lower lip morphology\n- Long face\n- Short chin\n- Microdontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Abnormality of the philtrum\n- Long philtrum\n- Bulbous nose\n- Anteverted nares\n- Abnormality iris morphology\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microdontia\n- Pectus excavatum\n- Hypotonia\n- Protuberant abdomen\n- Curly hair\n- Limb undergrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Widely spaced teeth\n- Microdontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Full cheeks\n- Bulbous nose\n- Flat face\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Full cheeks\n- Bulbous nose\n- Flat face\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Full cheeks\n- Bulbous nose\n- Flat face\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Long neck\n- Thick vermilion border\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Long neck\n- Thick vermilion border\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Long neck\n- Thick vermilion border\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Long neck\n- Thick vermilion border\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Long neck\n- Thick vermilion border\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Long neck\n- Thick vermilion border\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Brachycephaly\n- Malar flattening\n- Long philtrum\n- Downslanted palpebral fissures\n- Corneal scarring\n- Intellectual disability\n- Obesity\n- Hoarse voice\n- Bicuspid aortic valve\n- Aortic valve stenosis\n- Short foot\n- Clinodactyly of the 5th finger\n- Short stature\n- Prominent nasal tip\n- Stellate iris\n- Retinal vascular tortuosity\n- Irregular astigmatism\n- Overfriendliness\n- Kayser-Fleischer ring\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Epicanthus\n- Long philtrum\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Visual impairment\n- Photophobia\n- Periorbital fullness\n- Carious teeth\n- Hypoplasia of teeth\n- Widely spaced teeth\n- Delayed speech and language development\n- Pectus excavatum\n- Albinism\n- Intellectual disability\n- Umbilical hernia\n- Selective tooth agenesis\n- Hoarse voice\n- Congestive heart failure\n- Small nail\n- Anemia\n- Curly hair\n- Poor motor coordination\n- Supravalvular aortic stenosis\n- Depressed nasal bridge\n- Enamel hypomineralization\n- Anterior open-bite malocclusion\n- Medial flaring of the eyebrow\n- Hyperacusis\n- Midface retrusion\n- Stellate iris\n- Tongue thrusting\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Full cheeks\n- Abnormality of the chin\n- Long philtrum\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Full cheeks\n- Abnormality of the chin\n- Long philtrum\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Full cheeks\n- Abnormality of the chin\n- Long philtrum\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Pointed chin\n- Short chin\n- Broad forehead\n- Long philtrum\n- Anteverted nares\n- Periorbital fullness\n- Depressed nasal bridge\n- Thick vermilion border\n- Stellate iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Malar flattening\n- Epicanthus\n- Full cheeks\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Long neck\n- Strabismus\n- Periorbital fullness\n- Dental malocclusion\n- Intellectual disability, mild\n- Joint laxity\n- Hoarse voice\n- Short nose\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Large earlobe\n- Broad eyebrow\n- Thick vermilion border\n- Systolic heart murmur\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Narrow forehead\n- Long philtrum\n- Long neck\n- Strabismus\n- Dental malocclusion\n- Joint laxity\n- Hoarse voice\n- Prominent nasal tip\n- Large earlobe\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Long philtrum\n- Periorbital fullness\n- Global developmental delay\n- Constipation\n- Supernumerary nipple\n- Prominent nasal tip\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Microcephaly\n- Hypertension\n- Intellectual disability\n- Gastroesophageal reflux\n- Hiatus hernia\n- Short stature\n- Supravalvular aortic stenosis\n- Renal malrotation\n- Dysplastic sacrum\n- Feeding difficulties in infancy\n- Esophageal stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Oligomenorrhea\n- Lymphedema\n- Obesity\n- Decreased serum estradiol\n- Elevated circulating follicle stimulating hormone level\n- Mild global developmental delay\n- Stellate iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Oligomenorrhea\n- Lymphedema\n- Obesity\n- Decreased serum estradiol\n- Elevated circulating follicle stimulating hormone level\n- Mild global developmental delay\n- Stellate iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Oligomenorrhea\n- Lymphedema\n- Obesity\n- Decreased serum estradiol\n- Elevated circulating follicle stimulating hormone level\n- Mild global developmental delay\n- Stellate iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Oligomenorrhea\n- Lymphedema\n- Obesity\n- Decreased serum estradiol\n- Elevated circulating follicle stimulating hormone level\n- Mild global developmental delay\n- Stellate iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pelvic kidney\n- Microcephaly\n- Short stature\n- Decreased body weight\n- Supravalvular aortic stenosis\n- Pulmonary artery stenosis\n- Feeding difficulties in infancy\n- Hypoplastic aortic arch\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Tinnitus\n- Otosclerosis\n- Low-set ears\n- Protruding ear\n- Strabismus\n- Global developmental delay\n- Mitral regurgitation\n- Duodenal ulcer\n- Kyphoscoliosis\n- Genu valgum\n- Supravalvular aortic stenosis\n- Elfin facies\n- Bilateral conductive hearing impairment\n- Low-frequency hearing loss\n- Hyperacusis\n- Protruding tongue\n- Short palpebral fissure\n- Mid-frequency hearing loss\n- Abnormality of the acoustic reflex\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Hirsutism\n- Low posterior hairline\n- Depressed nasal bridge\n- Curly eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypogonadism\n- Thin vermilion border\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Carious teeth\n- Delayed eruption of teeth\n- Pectus excavatum\n- Cutis marmorata\n- Hirsutism\n- Short foot\n- Toe clinodactyly\n- Pneumonia\n- Language impairment\n- Hypoplastic nipples\n- Downturned corners of mouth\n- Micromelia\n- Short nose\n- Clinodactyly of the 5th finger\n- Malnutrition\n- Small hand\n- Abnormal mandibular symphysis morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Brachycephaly\n- Oxycephaly\n- Low anterior hairline\n- Micrognathia\n- Anteverted nares\n- Short neck\n- Megalocornea\n- Glaucoma\n- Cataract\n- Long eyelashes\n- Synophrys\n- Cyanosis\n- Hirsutism\n- Abnormally large globe\n- Seizure\n- Global developmental delay\n- Absent speech\n- Limited elbow extension\n- Short foot\n- Poor suck\n- Low posterior hairline\n- Recurrent respiratory infections\n- Short stature\n- Bilateral single transverse palmar creases\n- Clinodactyly\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Oxycephaly\n- Low anterior hairline\n- Micrognathia\n- Anteverted nares\n- Short neck\n- Glaucoma\n- Long eyelashes\n- Synophrys\n- Abnormality of the vertebral column\n- Cyanosis\n- Hirsutism\n- Seizure\n- Growth delay\n- Umbilical hernia\n- Short foot\n- Low posterior hairline\n- Downturned corners of mouth\n- Lumbar hemivertebrae\n- Intellectual disability, severe\n- Clinodactyly\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Highly arched eyebrow\n- High, narrow palate\n- Downturned corners of mouth\n- Short nasal bridge\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Depressed nasal ridge\n- Anteverted nares\n- Short neck\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Hirsutism\n- Small thenar eminence\n- Abnormality of the upper limb\n- Radial bowing\n- Dislocated radial head\n- Curved distal phalanx of the 5th finger\n- Aplasia\/Hypoplasia of the ulna\n- Curly eyelashes\n- Aplasia of the fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin vermilion border\n- Micrognathia\n- Hearing impairment\n- Abnormal morphology of the nasal alae\n- Synophrys\n- Single transverse palmar crease\n- Hirsutism\n- Short foot\n- Gastroesophageal reflux\n- Multiple renal cysts\n- Bilateral cryptorchidism\n- Wide nasal base\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Cutis marmorata\n- Hirsutism\n- Growth delay\n- Mitral regurgitation\n- Short foot\n- Talipes\n- Hyperkinetic movements\n- Short nose\n- Flat occiput\n- Proximal placement of thumb\n- Cutaneous syndactyly\n- Abnormal cry\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Synophrys\n- Cutis marmorata\n- Hirsutism\n- Global developmental delay\n- Growth delay\n- Short foot\n- Overlapping toe\n- Pyloric stenosis\n- Hyperkinetic movements\n- Short nose\n- Flat occiput\n- Bilateral single transverse palmar creases\n- Proximal placement of thumb\n- Cutaneous syndactyly\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Anteverted nares\n- Short neck\n- Abnormal eyebrow morphology\n- Curly eyelashes\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Anteverted nares\n- Short neck\n- Abnormal eyebrow morphology\n- Curly eyelashes\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Prominent nasal bridge\n- Thick eyebrow\n- Short nose\n- Prominent nasal tip\n- Abnormal jaw morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick eyebrow\n- Short nose\n- Prominent nasal tip\n- Everted upper lip vermilion\n- Laterally extended eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long philtrum\n- Long eyelashes\n- Synophrys\n- Micromelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Synophrys\n- Micromelia\n- Curly eyelashes\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long philtrum\n- Long eyelashes\n- Synophrys\n- Micromelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Long philtrum\n- Long eyelashes\n- Synophrys\n- Micromelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Downturned corners of mouth\n- Curly eyelashes\n- Proximal placement of thumb\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Downturned corners of mouth\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Nystagmus\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Dry skin\n- Global developmental delay\n- Cerebral cortical atrophy\n- Coarse hair\n- Abnormal sella turcica morphology\n- Delayed skeletal maturation\n- Increased blood urea nitrogen\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Duplicated colon\n- Depressed nasal bridge\n- Flat occiput\n- Limited elbow extension and supination\n- Bilateral single transverse palmar creases\n- Decreased testicular size\n- Feeding difficulties in infancy\n- Short 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short metacarpal\n- Stercoral ulcer\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Nystagmus\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Dry skin\n- Global developmental delay\n- Coarse hair\n- Abnormal sella turcica morphology\n- Delayed skeletal maturation\n- Increased blood urea nitrogen\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Flat occiput\n- Limited elbow extension and supination\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Short 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short metacarpal\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Nystagmus\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Dry skin\n- Global developmental delay\n- Hypoglycemia\n- Coarse hair\n- Delayed skeletal maturation\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Flat occiput\n- Limited elbow extension and supination\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Short 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short metacarpal\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Nystagmus\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Dry skin\n- Global developmental delay\n- Coarse hair\n- Delayed skeletal maturation\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Flat occiput\n- Limited elbow extension and supination\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Short 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short metacarpal\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Micropenis\n- Thin vermilion border\n- Microcephaly\n- Abnormal mastoid morphology\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Broad neck\n- Long eyelashes\n- Thick eyebrow\n- Osteoporosis\n- Single transverse palmar crease\n- Cutis marmorata\n- Hypertrichosis\n- Tapered finger\n- Delayed ossification of carpal bones\n- Small thenar eminence\n- Intellectual disability\n- Hypotonia\n- Growth delay\n- Umbilical hernia\n- Abnormal rib cage morphology\n- Barrel-shaped chest\n- Short foot\n- Short distal phalanx of toe\n- Dysphagia\n- Abnormality of skull ossification\n- Recurrent infections\n- Micromelia\n- Limited elbow movement\n- Hypoplasia of the ulna\n- Ulnar bowing\n- Short nose\n- Hypoplastic radial head\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Bilateral elbow dislocations\n- Depressed nasal bridge\n- Short middle phalanx of finger\n- Short finger\n- Proximal placement of thumb\n- Short 1st metacarpal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Single transverse palmar crease\n- Cutis marmorata\n- Hypertrichosis\n- Tapered finger\n- Small thenar eminence\n- Intellectual disability\n- Hypotonia\n- Growth delay\n- Abnormal heart morphology\n- Short foot\n- Overlapping toe\n- Dysphagia\n- High, narrow palate\n- Recurrent infections\n- Delayed skeletal maturation\n- Micromelia\n- Limited elbow movement\n- Dislocated radial head\n- Short nose\n- Hypoplastic radial head\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Short middle phalanx of finger\n- Chronic irritative conjunctivitis\n- Short finger\n- Short 2nd finger\n- Proximal placement of thumb\n- U-Shaped upper lip vermilion\n- Abnormal cry\n- Rhinorrhea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Broad neck\n- Long eyelashes\n- Microphthalmia\n- Thick eyebrow\n- Microdontia\n- Osteoporosis\n- Single transverse palmar crease\n- Hypertrichosis\n- Numerous nevi\n- Tapered finger\n- Growth delay\n- Barrel-shaped chest\n- Abnormal heart morphology\n- Short foot\n- Short distal phalanx of toe\n- Dysphagia\n- Episodic vomiting\n- Coxa valga\n- Abnormality of skull ossification\n- High, narrow palate\n- Recurrent infections\n- Micromelia\n- Limited elbow movement\n- Short nose\n- Marked delay in bone age\n- Clinodactyly of the 5th finger\n- Craniofacial asymmetry\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Flat occiput\n- Short middle phalanx of finger\n- Pseudoepiphyses of second metacarpal\n- Aplasia\/Hypoplasia involving the carpal bones\n- Chronic irritative conjunctivitis\n- Cone-shaped epiphysis of the middle phalanx of the 4th finger\n- Short 5th finger\n- Short 4th finger\n- Short finger\n- Cone-shaped epiphysis of the middle phalanx of the 2nd finger\n- Short 2nd finger\n- Proximal placement of thumb\n- Short 1st metacarpal\n- Enlarged epiphysis of the proximal phalanx of the hallux\n- Enlarged epiphysis of the distal phalanx of the hallux\n- Pseudoepiphysis of the 5th metacarpal\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Clinodactyly of the 4th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Microdontia\n- Osteoporosis\n- Single transverse palmar crease\n- Hypertrichosis\n- Tapered finger\n- Intellectual disability\n- Growth delay\n- Short foot\n- Hypophosphatemia\n- Coxa valga\n- High, narrow palate\n- Hypocalcemia\n- Micromelia\n- Limited elbow movement\n- Short nose\n- Low alkaline phosphatase\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Chronic irritative conjunctivitis\n- Short finger\n- Proximal placement of thumb\n- Deviation of the 2nd toe\n- Deviation of the 3rd toe\n- Deviation of the 4th toe\n- U-Shaped upper lip vermilion\n- EEG with generalized slow activity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Hypertrichosis\n- Tapered finger\n- Carpal bone hypoplasia\n- Growth delay\n- Barrel-shaped chest\n- Dysphagia\n- Coxa valga\n- Thickened calvaria\n- Micromelia\n- Radial bowing\n- Limited elbow movement\n- Hypoplasia of the ulna\n- Clinodactyly of the 5th finger\n- Short middle phalanx of finger\n- Short finger\n- Aplasia\/Hypoplasia of the middle phalanx of the 2nd finger\n- Proximal placement of thumb\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Microdontia\n- Cutis marmorata\n- Hypertrichosis\n- Tapered finger\n- Small thenar eminence\n- Growth delay\n- Barrel-shaped chest\n- Pes cavus\n- Short foot\n- Micromelia\n- Limited elbow movement\n- Hypoplasia of the ulna\n- Fibular hypoplasia\n- Short nose\n- Posteriorly dislocated ulna\n- Clinodactyly of the 5th finger\n- Short third metatarsal\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Short tibia\n- Finger joint hypermobility\n- Short finger\n- Proximal placement of thumb\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Decreased fibular diameter\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Microdontia\n- Osteoporosis\n- Single transverse palmar crease\n- Cutis marmorata\n- Numerous nevi\n- Tapered finger\n- Carpal bone hypoplasia\n- Growth delay\n- Barrel-shaped chest\n- Abnormal heart morphology\n- Pes cavus\n- Short foot\n- Dysphagia\n- Hiatus hernia\n- Intellectual disability, moderate\n- Episodic vomiting\n- Hypocalcemia\n- Micromelia\n- Fibular hypoplasia\n- Short nose\n- Marked delay in bone age\n- Clinodactyly of the 5th finger\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- Distal ulnar hypoplasia\n- Depressed nasal bridge\n- Short tibia\n- Aplasia\/Hypoplasia of the middle phalanx of the 5th finger\n- Short finger\n- Cone-shaped epiphysis of the middle phalanx of the 2nd finger\n- Aplasia\/Hypoplasia of the middle phalanx of the 2nd finger\n- Proximal placement of thumb\n- Short 1st metacarpal\n- Esophageal stenosis\n- Abnormality of the epiphysis of the femoral head\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Cleft palate\n- Abnormal upper lip morphology\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Osteoporosis\n- Cyanosis\n- Cutis marmorata\n- Hypertrichosis\n- Numerous nevi\n- Tapered finger\n- Intellectual disability\n- Hypotonia\n- Growth delay\n- High, narrow palate\n- Recurrent infections\n- Micromelia\n- Short nose\n- Marked delay in bone age\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Aplasia\/Hypoplasia of the middle phalanx of the 5th finger\n- Short finger\n- Aplasia\/Hypoplasia of the middle phalanx of the 2nd finger\n- Short distal phalanx of finger\n- U-Shaped upper lip vermilion\n- Rhinorrhea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Short neck\n- Broad neck\n- Long eyelashes\n- Thick eyebrow\n- Single transverse palmar crease\n- Numerous nevi\n- Tapered finger\n- Short foot\n- Delayed skeletal maturation\n- Micromelia\n- Radial bowing\n- Limited elbow movement\n- Dislocated radial head\n- Short nose\n- Hypoplastic radial head\n- Clinodactyly of the 5th finger\n- Lunate-triquetral fusion\n- 2-3 toe syndactyly\n- Supernumerary ribs\n- Short finger\n- Short metatarsal\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Broad neck\n- Long eyelashes\n- Thick eyebrow\n- Microdontia\n- Hypertrichosis\n- Tapered finger\n- Small thenar eminence\n- Hypotonia\n- Growth delay\n- Pes cavus\n- Spina bifida\n- Thickened calvaria\n- Recurrent infections\n- Kyphoscoliosis\n- Thoracic kyphosis\n- Micromelia\n- Limited elbow movement\n- Hypoplasia of the ulna\n- Short distal phalanx of the 3rd finger\n- Clinodactyly of the 5th finger\n- Short distal phalanx of the 5th finger\n- Hyperostosis frontalis interna\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- Short fifth metatarsal\n- Depressed nasal bridge\n- Finger joint hypermobility\n- Short distal phalanx of the 4th finger\n- Short finger\n- Short distal phalanx of the 2nd finger\n- Proximal placement of thumb\n- Symphalangism affecting the phalanges of the toes\n- Cutis gyrata of scalp\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Abnormality of vertebral epiphysis morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Cyanosis\n- Hypertrichosis\n- Numerous nevi\n- Tapered finger\n- Small thenar eminence\n- Growth delay\n- Short foot\n- Micromelia\n- Limited elbow movement\n- Hypoplasia of the ulna\n- Dislocated radial head\n- Posteriorly dislocated ulna\n- Hypoplastic radial head\n- Clinodactyly of the 5th finger\n- Short middle phalanx of the 5th finger\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- Short fifth metatarsal\n- Depressed nasal bridge\n- Finger joint hypermobility\n- Short finger\n- Proximal placement of thumb\n- Abnormal 5th metacarpal morphology\n- Aplasia\/Hypoplasia of the 1st metacarpal\n- Abnormality of the epiphyses of the 4th toe\n- Abnormality of the epiphyses of the 5th toe\n- Symphalangism affecting the phalanges of the 4th toe\n- Symphalangism affecting the phalanges of the 5th toe\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Rhinorrhea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Hypertrichosis\n- Tapered finger\n- Hypotonia\n- Growth delay\n- Sandal gap\n- EEG abnormality\n- Recurrent infections\n- Micromelia\n- Dislocated radial head\n- Hypoplastic radial head\n- Clinodactyly of the 5th finger\n- Short middle phalanx of the 5th finger\n- Lunate-triquetral fusion\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- 2-3 toe cutaneous syndactyly\n- Short humerus\n- Short finger\n- Short middle phalanx of the 2nd finger\n- Proximal placement of thumb\n- Forearm undergrowth\n- Short 1st metacarpal\n- Short 4th metacarpal\n- Short 5th metacarpal\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Low-set ears\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Delayed eruption of teeth\n- Microdontia\n- Abnormal thorax morphology\n- Abnormal sternum morphology\n- Single transverse palmar crease\n- Hypertrichosis\n- Hypotonia\n- Carpal bone hypoplasia\n- Growth delay\n- Abnormal heart morphology\n- Ventricular septal defect\n- Pulmonic stenosis\n- Right ventricular hypertrophy\n- Left ventricular hypertrophy\n- Dysphagia\n- Pulmonary hypoplasia\n- Episodic vomiting\n- High, narrow palate\n- Recurrent infections\n- Kyphoscoliosis\n- Sudden episodic apnea\n- Thoracic kyphosis\n- Hypoplasia of the radius\n- Limited elbow movement\n- Dislocated radial head\n- Marked delay in bone age\n- Aplasia of the ulna\n- Hypoplastic radial head\n- Lunate-triquetral fusion\n- Short third metatarsal\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- Short fifth metatarsal\n- Aplasia of the 5th finger\n- Aplasia of the 4th finger\n- Aplasia of the 3rd finger\n- Abnormality of the distal radial epiphysis\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Esophageal leukoplakia\n- Pulmonary edema\n- Abnormality of vertebral epiphysis morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal upper lip morphology\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Broad neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Delayed eruption of teeth\n- Single transverse palmar crease\n- Hypertrichosis\n- Tapered finger\n- Small thenar eminence\n- Intellectual disability\n- Growth delay\n- Short foot\n- Dysphagia\n- High, narrow palate\n- Thoracic kyphosis\n- Micromelia\n- Limited elbow movement\n- Hypoplasia of the ulna\n- Dislocated radial head\n- Low alkaline phosphatase\n- Hypoplastic radial head\n- Clinodactyly of the 5th finger\n- Short middle phalanx of the 5th finger\n- Short third metatarsal\n- Short fourth metatarsal\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Single interphalangeal crease of fifth finger\n- Short finger\n- Short middle phalanx of the 2nd finger\n- Proximal placement of thumb\n- Aplasia\/Hypoplasia of the phalanges of the thumb\n- Short 1st metacarpal\n- Symphalangism affecting the phalanges of the 3rd toe\n- Symphalangism affecting the phalanges of the 4th toe\n- Symphalangism affecting the phalanges of the 5th toe\n- U-Shaped upper lip vermilion\n- Right bundle branch block\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Small forehead\n- Posteriorly rotated ears\n- Flared nostrils\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Autism\n- Aggressive behavior\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Hypertrophic cardiomyopathy\n- Achilles tendon contracture\n- Pyloric stenosis\n- Coarse hair\n- Highly arched eyebrow\n- Supernumerary nipple\n- Short nose\n- Short palm\n- Increased dermatoglyphic whorls\n- Bilateral single transverse palmar creases\n- Repetitive compulsive behavior\n- Short 1st metacarpal\n- Abnormally low-pitched voice\n- U-Shaped upper lip vermilion\n- Long upper lip\n- Mild global developmental delay\n- Abnormal sternal ossification\n- Manifestations of perseverative thought or action\n- Self-injurious behavior\n- Lip cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Synophrys\n- Single transverse palmar crease\n- Cutis marmorata\n- Hypertrichosis\n- Small thenar eminence\n- Motor delay\n- Small for gestational age\n- Metatarsus adductus\n- Intellectual disability, moderate\n- Elbow flexion contracture\n- Dislocated radial head\n- Short nose\n- Birth length less than 3rd percentile\n- Short palm\n- Short stature\n- Decreased body weight\n- Complex palmar dermatoglyphic pattern\n- Short 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Brachycephaly\n- Microcephaly\n- Posteriorly rotated ears\n- Anteverted nares\n- Synophrys\n- Cyanosis\n- 2-3 finger syndactyly\n- Hypotonia\n- Ventricular septal defect\n- Short foot\n- Short toe\n- Deep philtrum\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Sudden episodic apnea\n- Micromelia\n- Fractures of the long bones\n- Clinodactyly of the 5th finger\n- Short palm\n- Prominent nasolabial fold\n- Flat occiput\n- Abnormal metacarpal morphology\n- Hypoplasia of proximal radius\n- Recurrent pneumonia\n- Aplasia of the 4th finger\n- Short finger\n- Proximal placement of thumb\n- Short thumb\n- Abnormal middle phalanx morphology of the hand\n- Abnormal proximal phalanx morphology of the hand\n- Curved 1st metacarpal\n- Short 1st metacarpal\n- U-Shaped upper lip vermilion\n- Prominent forehead\n- Feeding difficulties\n- Short palpebral fissure\n- Systolic heart murmur\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Posteriorly rotated ears\n- Long eyelashes\n- Synophrys\n- Hypertrichosis\n- Absent speech\n- Short foot\n- Short toe\n- Deep philtrum\n- Highly arched eyebrow\n- Radial bowing\n- Clinodactyly of the 5th finger\n- Short middle phalanx of the 5th finger\n- Short palm\n- Bilateral single transverse palmar creases\n- Microtia\n- Curved middle phalanx of the 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short thumb\n- Abnormal 5th metacarpal morphology\n- Curved 1st metacarpal\n- Short 1st metacarpal\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Posteriorly rotated ears\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Short foot\n- Short toe\n- Highly arched eyebrow\n- Clinodactyly of the 5th finger\n- Short middle phalanx of the 5th finger\n- Short palm\n- Curved middle phalanx of the 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short thumb\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Prominent forehead\n- Short palpebral fissure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Brachycephaly\n- Microcephaly\n- Posteriorly rotated ears\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Short foot\n- Short toe\n- Deep philtrum\n- Highly arched eyebrow\n- Clinodactyly of the 5th finger\n- Short palm\n- Prominent nasolabial fold\n- Short finger\n- Proximal placement of thumb\n- Short thumb\n- Short 1st metacarpal\n- Prominent forehead\n- Short palpebral fissure\n- obsolete Small scrotum\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Posteriorly rotated ears\n- Long eyelashes\n- Synophrys\n- Single transverse palmar crease\n- Short toe\n- Deep philtrum\n- Highly arched eyebrow\n- Abnormality of the lower limb\n- Clinodactyly of the 5th finger\n- Short palm\n- Microtia\n- Short finger\n- Proximal placement of thumb\n- Short thumb\n- Short 1st metacarpal\n- Prominent forehead\n- Short palpebral fissure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Posteriorly rotated ears\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability, mild\n- Global developmental delay\n- Growth delay\n- Generalized hirsutism\n- Clinodactyly of the 5th finger\n- Short stature\n- Limited pronation\/supination of forearm\n- Bilateral single transverse palmar creases\n- Microtia\n- Short 5th finger\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Posteriorly rotated ears\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability, mild\n- Global developmental delay\n- Growth delay\n- Generalized hirsutism\n- Clinodactyly of the 5th finger\n- Short stature\n- Limited pronation\/supination of forearm\n- Bilateral single transverse palmar creases\n- Microtia\n- Short 5th finger\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Hyporeflexia\n- Motor delay\n- Hypertonia\n- Growth delay\n- Gastroesophageal reflux\n- Expressive language delay\n- Episodic vomiting\n- Kyphoscoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Decreased body weight\n- Malrotation of colon\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Speech articulation difficulties\n- Triangular shaped middle phalanx of the 5th finger\n- Joint contracture of the 5th finger\n- Short 5th finger\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Skin tags\n- Tented upper lip vermilion\n- Feeding difficulties\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Hyporeflexia\n- Motor delay\n- Hypertonia\n- Growth delay\n- Gastroesophageal reflux\n- Expressive language delay\n- Episodic vomiting\n- Kyphoscoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Decreased body weight\n- Malrotation of colon\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Speech articulation difficulties\n- Triangular shaped middle phalanx of the 5th finger\n- Joint contracture of the 5th finger\n- Short 5th finger\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Skin tags\n- Tented upper lip vermilion\n- Feeding difficulties\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Hyporeflexia\n- Motor delay\n- Hypertonia\n- Growth delay\n- Gastroesophageal reflux\n- Expressive language delay\n- Episodic vomiting\n- Kyphoscoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Decreased body weight\n- Malrotation of colon\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Speech articulation difficulties\n- Triangular shaped middle phalanx of the 5th finger\n- Joint contracture of the 5th finger\n- Short 5th finger\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Skin tags\n- Tented upper lip vermilion\n- Feeding difficulties\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Hyporeflexia\n- Motor delay\n- Hypertonia\n- Growth delay\n- Gastroesophageal reflux\n- Expressive language delay\n- Episodic vomiting\n- Kyphoscoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Decreased body weight\n- Malrotation of colon\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Speech articulation difficulties\n- Triangular shaped middle phalanx of the 5th finger\n- Joint contracture of the 5th finger\n- Short 5th finger\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Skin tags\n- Tented upper lip vermilion\n- Feeding difficulties\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Hyporeflexia\n- Motor delay\n- Hypertonia\n- Growth delay\n- Gastroesophageal reflux\n- Expressive language delay\n- Episodic vomiting\n- Kyphoscoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Decreased body weight\n- Malrotation of colon\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Speech articulation difficulties\n- Triangular shaped middle phalanx of the 5th finger\n- Joint contracture of the 5th finger\n- Short 5th finger\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Skin tags\n- Tented upper lip vermilion\n- Feeding difficulties\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Triangular nasal tip\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Hyporeflexia\n- Motor delay\n- Hypertonia\n- Growth delay\n- Gastroesophageal reflux\n- Expressive language delay\n- Episodic vomiting\n- Kyphoscoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Decreased body weight\n- Malrotation of colon\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Speech articulation difficulties\n- Triangular shaped middle phalanx of the 5th finger\n- Joint contracture of the 5th finger\n- Short 5th finger\n- Short 1st metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Skin tags\n- Tented upper lip vermilion\n- Feeding difficulties\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Strabismus\n- Synophrys\n- Irritability\n- 2-3 finger syndactyly\n- Hypotonia\n- Global developmental delay\n- Hypoglycemia\n- Generalized hirsutism\n- Episodic vomiting\n- Short palm\n- Short finger\n- Short phalanx of finger\n- Small hypothenar eminence\n- Tented upper lip vermilion\n- Feeding difficulties\n- Cognitive impairment\n- Hypoplastic areola\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/01550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Widow's peak\n- Synophrys\n- Cutis marmorata\n- Hypertrichosis\n- Hirsutism\n- Absent speech\n- Growth delay\n- Small for gestational age\n- Exaggerated cupid's bow\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Stiff interphalangeal joints\n- Short 3rd toe\n- Bilateral single transverse palmar creases\n- Short 5th finger\n- Short 2nd finger\n- Short thumb\n- Intellectual disability, severe\n- Prominent eyelashes\n- Severe global developmental delay\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Ptosis\n- Myopia\n- Photophobia\n- Nystagmus\n- Synophrys\n- Brachydactyly\n- Intellectual disability, mild\n- Single interphalangeal crease of fifth finger\n- Short 2nd finger\n- Localized hirsutism\n- Short 5th toe\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Synophrys\n- Single transverse palmar crease\n- Brachydactyly\n- Intellectual disability, mild\n- Growth delay\n- Small for gestational age\n- Short foot\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Single interphalangeal crease of fifth finger\n- Short 5th finger\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- High palate\n- Widow's peak\n- Small forehead\n- Prominent nasal bridge\n- Synophrys\n- Delayed speech and language development\n- Hirsutism\n- Brachydactyly\n- Short foot\n- Athetosis\n- Highly arched eyebrow\n- Limited elbow movement\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- 2-3 toe syndactyly\n- Single interphalangeal crease of fifth finger\n- Intellectual disability, severe\n- Delayed ability to walk\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Abnormal external genitalia\n- Hirsutism\n- Intellectual disability\n- Intrauterine growth retardation\n- Short foot\n- Downturned corners of mouth\n- Abnormality of the musculature\n- Short nose\n- Depressed nasal bridge\n- Postnatal growth retardation\n- obsolete Psychomotor retardation\n- Abnormal cry\n- Abnormality of limbs\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Cutis marmorata\n- Hirsutism\n- Intellectual disability\n- Short foot\n- Hypoplastic nipples\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Postnatal growth retardation\n- Proximal placement of thumb\n- obsolete Psychomotor retardation\n- Abnormal cry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Intellectual disability\n- Intrauterine growth retardation\n- Short foot\n- Hypoplastic nipples\n- Downturned corners of mouth\n- Limited elbow movement\n- Short nose\n- Clinodactyly of the 5th finger\n- Short palm\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Proximal placement of thumb\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Cutis marmorata\n- Hirsutism\n- Intellectual disability\n- High, narrow palate\n- Postnatal growth retardation\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Cutis marmorata\n- Intellectual disability\n- Short foot\n- Hypoplastic nipples\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Proximal placement of thumb\n- obsolete Psychomotor retardation\n- Abnormal cry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin vermilion border\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Cutis marmorata\n- Hirsutism\n- Intellectual disability\n- Intrauterine growth retardation\n- Short foot\n- Downturned corners of mouth\n- Short nose\n- Clinodactyly of the 5th finger\n- Short palm\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Proximal placement of thumb\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Highly arched eyebrow\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Cutis marmorata\n- Intellectual disability\n- Motor delay\n- Failure to thrive\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin vermilion border\n- Microcephaly\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Delayed speech and language development\n- Single transverse palmar crease\n- Seizure\n- Intellectual disability, mild\n- Toe syndactyly\n- Short foot\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Depressed nasal bridge\n- Lacrimal duct stenosis\n- Feeding difficulties in infancy\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypospadias\n- Cleft palate\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Motor delay\n- Small for gestational age\n- Short foot\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Proximal placement of thumb\n- Wheezing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Low-set ears\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Autistic behavior\n- Delayed speech and language development\n- Cutis marmorata\n- Motor delay\n- Short foot\n- Asthma\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Lacrimal duct stenosis\n- Proximal placement of thumb\n- Simple febrile seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Cutis marmorata\n- Hirsutism\n- Seizure\n- Motor delay\n- Short foot\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Limited elbow movement\n- Depressed nasal bridge\n- Unilateral oligodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Horizontal nystagmus\n- Delayed speech and language development\n- Hirsutism\n- Hallux valgus\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n- Proximal placement of thumb\n- Vertical nystagmus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormal testis morphology\n- Hypospadias\n- Thin upper lip vermilion\n- Long philtrum\n- Anteverted nares\n- Synophrys\n- Seizure\n- Absent speech\n- Short foot\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short nose\n- Short palm\n- Postnatal growth retardation\n- Short 5th finger\n- Concave nasal ridge\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Sensorineural hearing impairment\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Cyanosis\n- Hypertrichosis\n- Hypertonia\n- Failure to thrive\n- Episodic vomiting\n- Neonatal respiratory distress\n- Downturned corners of mouth\n- Micromelia\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Feeding difficulties\n- Acute respiratory distress syndrome\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Sensorineural hearing impairment\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Cyanosis\n- Hypertrichosis\n- Hypertonia\n- Failure to thrive\n- Episodic vomiting\n- Neonatal respiratory distress\n- Downturned corners of mouth\n- Micromelia\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Feeding difficulties\n- Acute respiratory distress syndrome\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Sensorineural hearing impairment\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Single transverse palmar crease\n- Cyanosis\n- Hypertrichosis\n- Hypertonia\n- Failure to thrive\n- Episodic vomiting\n- Neonatal respiratory distress\n- Downturned corners of mouth\n- Micromelia\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Feeding difficulties\n- Acute respiratory distress syndrome\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Low-set ears\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Single transverse palmar crease\n- Hirsutism\n- Abnormal finger morphology\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Abnormal finger morphology\n- Intellectual disability, moderate\n- Depressed nasal bridge\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Hirsutism\n- Abnormal finger morphology\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Low-set ears\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Single transverse palmar crease\n- Hirsutism\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Deep philtrum\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short nose\n- Decreased body weight\n- 2-3 toe syndactyly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Deep philtrum\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short nose\n- Decreased body weight\n- 2-3 toe syndactyly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Global developmental delay\n- Specific learning disability\n- Growth delay\n- Subvalvular aortic stenosis\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Long nose\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Global developmental delay\n- Specific learning disability\n- Growth delay\n- Subvalvular aortic stenosis\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Long nose\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Cleft palate\n- Thin upper lip vermilion\n- Long philtrum\n- Micrognathia\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Cyanosis\n- Hypertonia\n- Abnormality of the larynx\n- Gastroesophageal reflux\n- Generalized hirsutism\n- Neonatal respiratory distress\n- Downturned corners of mouth\n- Upper airway obstruction\n- Micromelia\n- Elbow flexion contracture\n- Feeding difficulties\n- Low 1-minute APGAR score\n- 5-minute APGAR score of 4\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Cleft palate\n- Thin upper lip vermilion\n- Long philtrum\n- Micrognathia\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Cyanosis\n- Hypertonia\n- Abnormality of the larynx\n- Gastroesophageal reflux\n- Generalized hirsutism\n- Neonatal respiratory distress\n- Downturned corners of mouth\n- Upper airway obstruction\n- Micromelia\n- Elbow flexion contracture\n- Feeding difficulties\n- Low 1-minute APGAR score\n- 5-minute APGAR score of 4\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Cutis marmorata\n- Hand oligodactyly\n- Intellectual disability\n- Global developmental delay\n- Growth delay\n- Atrial septal defect\n- Deep philtrum\n- Dysphagia\n- Low posterior hairline\n- Generalized hirsutism\n- Poor speech\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Fibular hypoplasia\n- Short stature\n- Depressed nasal bridge\n- Aplasia\/hypoplasia involving bones of the lower limbs\n- Feeding difficulties in infancy\n- Postnatal growth retardation\n- Absent tibia\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Shawl scrotum\n- Micropenis\n- Thin upper lip vermilion\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Long eyelashes\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Dysphagia\n- Highly arched eyebrow\n- Mild short stature\n- Short palm\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Postnatal growth retardation\n- Short 1st metacarpal\n- Feeding difficulties\n- Small superior frontal cortex\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Shawl scrotum\n- Micropenis\n- Thin upper lip vermilion\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Long eyelashes\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Dysphagia\n- Highly arched eyebrow\n- Mild short stature\n- Short palm\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Postnatal growth retardation\n- Short 1st metacarpal\n- Feeding difficulties\n- Small superior frontal cortex\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Long philtrum\n- Anteverted nares\n- Webbed neck\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Atypical behavior\n- Cutis marmorata\n- Intellectual disability\n- Global developmental delay\n- Absent speech\n- Intrauterine growth retardation\n- Dysphagia\n- Gastroesophageal reflux\n- Low posterior hairline\n- Generalized hirsutism\n- Highly arched eyebrow\n- Recurrent infections\n- Limited elbow movement\n- Short middle phalanx of the 5th finger\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Feeding difficulties\n- Delayed ability to walk\n- Tube feeding\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Absent forearm\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Absent forearm\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Absent forearm\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Sinusitis\n- Long philtrum\n- Synophrys\n- Cutis marmorata\n- Flexion contracture\n- Bilateral ptosis\n- Mitral regurgitation\n- Hallux valgus\n- Gastroesophageal reflux\n- Hiatus hernia\n- Kyphoscoliosis\n- Short nose\n- Skeletal muscle atrophy\n- Severe short stature\n- Decreased body weight\n- Abnormality of the pylorus\n- Absent forearm\n- Lacrimal duct stenosis\n- Epiphora\n- Feeding difficulties\n- Chronic constipation\n- Neurodevelopmental abnormality\n- Cutaneous cyst\n- Barrett esophagus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/01601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the skeletal system\n- Prominent fingertip pads\n- Intellectual disability\n- Hypoplasia of the corpus callosum\n- Focal-onset seizure\n- Postnatal growth retardation\n- Dialeptic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the skeletal system\n- Prominent fingertip pads\n- Intellectual disability\n- Postnatal growth retardation\n- Anterior pituitary hypoplasia\n- EEG with spike-wave complexes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Cleft palate\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Ventricular septal defect\n- Anal atresia\n- EEG abnormality\n- Highly arched eyebrow\n- Aortic aneurysm\n- Sparse lateral eyebrow\n- Duplication of renal pelvis\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Abnormality of retinal pigmentation\n- Acetabular dysplasia\n- Postnatal growth retardation\n- Short metacarpal\n- Abnormality of the curvature of the vertebral column\n- Rectovestibular fistula\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Cervical ribs\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Atrial septal defect\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Short metacarpal\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Cervical ribs\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- High pitched voice\n- Coarctation of aorta\n- Dilated fourth ventricle\n- Highly arched eyebrow\n- Coxa valga\n- Delayed skeletal maturation\n- Sparse lateral eyebrow\n- Twelfth rib hypoplasia\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Premature thelarche\n- Abnormality of the curvature of the vertebral column\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Decreased response to growth hormone stimulation test\n- Abnormality of the skeletal system\n- Brachydactyly\n- Seizure\n- Intellectual disability, mild\n- Premature birth\n- Small nail\n- Neonatal hypoglycemia\n- Spina bifida\n- Highly arched eyebrow\n- Delayed skeletal maturation\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Missing ribs\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Twelfth rib hypoplasia\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Abnormality of the diaphragm\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Seizure\n- Umbilical hernia\n- Pes planus\n- Highly arched eyebrow\n- Butterfly vertebrae\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Abnormality of the skeletal system\n- Brachydactyly\n- Intellectual disability\n- Mild postnatal growth retardation\n- Ventricular septal defect\n- Highly arched eyebrow\n- Butterfly vertebrae\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Protruding ear\n- Depressed nasal tip\n- Microcornea\n- Long palpebral fissure\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Umbilical hernia\n- Highly arched eyebrow\n- Butterfly vertebrae\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Abnormality of the curvature of the vertebral column\n- Cervical aortic arch\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Abnormality of the curvature of the vertebral column\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Cervical ribs\n- Abnormality of the skeletal system\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Umbilical hernia\n- Premature birth\n- Tetralogy of Fallot\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Abnormal dermatoglyphics\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Proximal placement of thumb\n- Premature thelarche\n- Abnormal elasticity of skin\n- Abnormality of the curvature of the vertebral column\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Absent speech\n- Small nail\n- Constipation\n- Aganglionic megacolon\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Clinodactyly of the 5th finger\n- Short distal phalanx of finger\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Brachydactyly\n- Delayed ossification of carpal bones\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Absent speech\n- Small nail\n- Constipation\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Moderate sensorineural hearing impairment\n- Short distal phalanx of finger\n- Severe global developmental delay\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Smooth philtrum\n- Strabismus\n- Ptosis\n- Aggressive behavior\n- Delayed speech and language development\n- Hypotonia\n- Tremor\n- Mitral regurgitation\n- Pes cavus\n- Pes planus\n- Gait ataxia\n- Delayed gross motor development\n- Drooling\n- Incomprehensible speech\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Enlarged posterior fossa\n- Gait instability, worse in the dark\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Uplifted earlobe\n- Intellectual disability, severe\n- Impulsivity\n- Self-injurious behavior\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/01633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Narrow forehead\n- Low-set, posteriorly rotated ears\n- Prominent antihelix\n- Underdeveloped nasal alae\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Global developmental delay\n- Hypoplastic toenails\n- Frontal bossing\n- Delayed gross motor development\n- Sparse scalp hair\n- Highly arched eyebrow\n- Prominent nasal tip\n- Hypoplastic fifth toenail\n- Onychomadesis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macrocephaly\n- Full cheeks\n- Long palpebral fissure\n- Oculomotor apraxia\n- Microdontia\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Ataxia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Joint hypermobility\n- Elevated circulating alkaline phosphatase concentration\n- Microtia\n- Tented upper lip vermilion\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Cleft palate\n- Bifid uvula\n- Thin upper lip vermilion\n- Macrocephaly\n- Short philtrum\n- Wide nasal bridge\n- Deeply set eye\n- Upslanted palpebral fissure\n- Synophrys\n- Aggressive behavior\n- Autistic behavior\n- Seizure\n- Global developmental delay\n- Motor delay\n- Obesity\n- Sleep disturbance\n- Loss of speech\n- Elevated circulating alkaline phosphatase concentration\n- Attention deficit hyperactivity disorder\n- Thin lower lip vermilion\n- Osteochondritis dissecans\n- Prominence of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macrocephaly\n- Coarse facial features\n- Full cheeks\n- Short philtrum\n- Long palpebral fissure\n- Oculomotor apraxia\n- Seizure\n- Ataxia\n- Global developmental delay\n- Motor delay\n- Reduced tendon reflexes\n- Absent speech\n- Joint hypermobility\n- Elevated circulating alkaline phosphatase concentration\n- Gait instability, worse in the dark\n- Tented upper lip vermilion\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- High palate\n- Thin upper lip vermilion\n- Delayed cranial suture closure\n- Abnormality of the philtrum\n- Short chin\n- Narrow forehead\n- Micrognathia\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Long eyelashes\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Impaired social interactions\n- Global developmental delay\n- Small nail\n- Sudden episodic apnea\n- Radioulnar synostosis\n- Short palm\n- Overfolding of the superior helices\n- Prominent nasal tip\n- Low hanging columella\n- Short thumb\n- Medial flaring of the eyebrow\n- Prominent forehead\n- Tube feeding\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad forehead\n- Visual impairment\n- Hypotonia\n- Joint laxity\n- Hypoplasia of the corpus callosum\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/01639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Broad forehead\n- Low-set ears\n- Thickened helices\n- Short neck\n- Downslanted palpebral fissures\n- Ptosis\n- Failure to thrive\n- Pulmonic stenosis\n- Curly hair\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/01640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Prominent supraorbital ridges\n- Strabismus\n- Developmental cataract\n- Synophrys\n- Autistic behavior\n- Polyneuropathy\n- Absent speech\n- Subcutaneous calcification\n- Congenital sensorineural hearing impairment\n- Abnormality of hair pigmentation\n- Sunken cheeks\n- Intellectual disability, severe\n- Severe global developmental delay\n- Round ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/01641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Prominent supraorbital ridges\n- Strabismus\n- Developmental cataract\n- Synophrys\n- Autistic behavior\n- Polyneuropathy\n- Absent speech\n- Subcutaneous calcification\n- Congenital sensorineural hearing impairment\n- Abnormality of hair pigmentation\n- Sunken cheeks\n- Intellectual disability, severe\n- Severe global developmental delay\n- Round ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/01642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Prominent supraorbital ridges\n- Developmental cataract\n- Polyneuropathy\n- Subcutaneous calcification\n- Congenital sensorineural hearing impairment\n- Abnormality of hair pigmentation\n- Sunken cheeks\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/01643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Prominent supraorbital ridges\n- Developmental cataract\n- Polyneuropathy\n- Subcutaneous calcification\n- Congenital sensorineural hearing impairment\n- Abnormality of hair pigmentation\n- Sunken cheeks\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/01644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Prominent supraorbital ridges\n- Strabismus\n- Developmental cataract\n- Autistic behavior\n- Subcutaneous calcification\n- Congenital sensorineural hearing impairment\n- Sunken cheeks\n- Severe global developmental delay\n- Morphological abnormality of the lateral semicircular canal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/01645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Prominent supraorbital ridges\n- Strabismus\n- Developmental cataract\n- Autistic behavior\n- Subcutaneous calcification\n- Congenital sensorineural hearing impairment\n- Sunken cheeks\n- Severe global developmental delay\n- Morphological abnormality of the lateral semicircular canal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/01646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Long face\n- Pointed chin\n- Short philtrum\n- Anteverted nares\n- Strabismus\n- Hypermetropia\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Umbilical hernia\n- Weight loss\n- Vomiting\n- Gait ataxia\n- Global brain atrophy\n- Cortical dysplasia\n- Short nose\n- Flat occiput\n- Impaired pain sensation\n- Feeding difficulties in infancy\n- Axial hypotonia\n- Simplified gyral pattern\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Severe global developmental delay\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Brachycephaly\n- Epicanthus\n- Low anterior hairline\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Wide nasal bridge\n- Visual impairment\n- Upslanted palpebral fissure\n- Microdontia\n- Diastema\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Umbilical hernia\n- Recurrent aspiration pneumonia\n- Apnea\n- Frontal upsweep of hair\n- Recurrent infections\n- Short stature\n- Severe muscular hypotonia\n- Impaired pain sensation\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Delayed myelination\n- Nocturnal seizures\n- Tube feeding\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Long face\n- Pointed chin\n- Short philtrum\n- Low-set ears\n- Strabismus\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Slurred speech\n- Joint hypermobility\n- Failure to thrive\n- Dysphagia\n- Hypothermia\n- Recurrent infections\n- Excessive salivation\n- Short stature\n- Decreased body weight\n- Chronic gastritis\n- Flat occiput\n- Widely-spaced incisors\n- Impaired pain sensation\n- High hypermetropia\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Facial hypotonia\n- Short philtrum\n- Chronic otitis media\n- Wide nasal bridge\n- Short neck\n- Thickened nuchal skin fold\n- Astigmatism\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Microdontia\n- Diastema\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Dysarthria\n- Motor delay\n- Generalized hypotonia\n- Dysphagia\n- Gastroesophageal reflux\n- Broad-based gait\n- Unsteady gait\n- Intellectual disability, moderate\n- Sleep disturbance\n- Abnormal cortical gyration\n- Recurrent infections\n- Excessive salivation\n- Impaired pain sensation\n- Eversion of lateral third of lower eyelids\n- High hypermetropia\n- Enlarged labia minora\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Delayed fine motor development\n- Nasogastric tube feeding in infancy\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Epicanthus\n- Facial hypotonia\n- Pointed chin\n- Short philtrum\n- Low-set ears\n- Prominent nose\n- Hypermetropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Slurred speech\n- Unsteady gait\n- Intellectual disability, moderate\n- Excessive salivation\n- Impaired pain sensation\n- Axial hypotonia\n- Tented upper lip vermilion\n- Overweight\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Pointed chin\n- Hypertelorism\n- Long philtrum\n- Prominent nose\n- Broad nasal tip\n- Hypermetropia\n- Microdontia\n- Autistic behavior\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Myopathic facies\n- Abnormality of speech or vocalization\n- Unsteady gait\n- Long nose\n- Excessive salivation\n- Multiple cafe-au-lait spots\n- Narrow palpebral fissure\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Long philtrum\n- Prominent nose\n- Hypodontia\n- Abnormal dental enamel morphology\n- Tapered finger\n- Intellectual disability\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Chronic diarrhea\n- Abnormality of speech or vocalization\n- Recurrent infections\n- Low hanging columella\n- Thin lower lip vermilion\n- Narrow palpebral fissure\n- Thin eyebrow\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Retrognathia\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Stenosis of the external auditory canal\n- Prominent nose\n- Hypermetropia\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Hypertonia\n- Dysphagia\n- Gastroesophageal reflux\n- Myopathic facies\n- Asthma\n- Abnormality of speech or vocalization\n- Opisthotonus\n- Recurrent infections\n- Tracheomalacia\n- Feeding difficulties\n- Narrow palpebral fissure\n- Thin eyebrow\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Intellectual disability\n- Motor delay\n- Myopathic facies\n- Abnormality of speech or vocalization\n- Hypsarrhythmia\n- Secondary microcephaly\n- Medullary nephrocalcinosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Posteriorly rotated ears\n- Prominent nose\n- Anteverted nares\n- Upslanted palpebral fissure\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Abnormal foot morphology\n- Toe syndactyly\n- Gastroesophageal reflux\n- Pyloric stenosis\n- Myopathic facies\n- Asthma\n- Abnormality of speech or vocalization\n- Downturned corners of mouth\n- Aspiration\n- Finger syndactyly\n- Sleep apnea\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Midface retrusion\n- Feeding difficulties\n- Allergy\n- Bitemporal hollowing\n- Abnormally low T cell receptor excision circle level\n- Eosinophilic dermal infiltration\n- Narrow palpebral fissure\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Pointed chin\n- Prominent nose\n- Broad nasal tip\n- Myopia\n- Upslanted palpebral fissure\n- Microdontia\n- Asthma\n- Abnormality of speech or vocalization\n- Intellectual disability, moderate\n- Recurrent infections\n- Hyperglycemia\n- Short stature\n- Maturity-onset diabetes of the young\n- Bronchiolitis\n- Allergy\n- Stuttering\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Short philtrum\n- High forehead\n- Underdeveloped nasal alae\n- Deeply set eye\n- Autistic behavior\n- Impaired social interactions\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Abnormality of speech or vocalization\n- Allergy\n- Stuttering\n- Abnormal amygdala morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/01658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Depressed nasal tip\n- Broad nasal tip\n- Short neck\n- Myopia\n- Aggressive behavior\n- Global developmental delay\n- Generalized hypotonia\n- Joint laxity\n- Obesity\n- Broad-based gait\n- Sleep disturbance\n- Waddling gait\n- Downturned corners of mouth\n- Obstructive sleep apnea\n- Overfolding of the superior helices\n- Midface retrusion\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/01659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Webbed neck\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Visual impairment\n- Impaired social interactions\n- Congenital diaphragmatic hernia\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Wormian bones\n- Downturned corners of mouth\n- Short stature\n- Depressed nasal bridge\n- Poor fine motor coordination\n- Sparse hair\n- Hypoplastic cervical vertebrae\n- Moderate expressive language delay\n- Delayed myelination\n- Impairment of activities of daily living\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Malar flattening\n- Short philtrum\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Hypermetropia\n- Atypical behavior\n- Brachydactyly\n- Abnormal thumb morphology\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Widely-spaced maxillary central incisors\n- Atrial septal defect\n- Broad foot\n- Abnormal toe morphology\n- Poor suck\n- Focal impaired awareness seizure\n- Downturned corners of mouth\n- Motor tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Malar flattening\n- Short philtrum\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Hypermetropia\n- Atypical behavior\n- Brachydactyly\n- Abnormal thumb morphology\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Widely-spaced maxillary central incisors\n- Atrial septal defect\n- Broad foot\n- Abnormal toe morphology\n- Poor suck\n- Focal impaired awareness seizure\n- Downturned corners of mouth\n- Motor tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Cleft palate\n- High palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Broad forehead\n- Micrognathia\n- Hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Exotropia\n- Optic nerve hypoplasia\n- Brachydactyly\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Atrial septal defect\n- Patent foramen ovale\n- Ventriculomegaly\n- Abnormal cerebral white matter morphology\n- Downturned corners of mouth\n- Immunodeficiency\n- Short palm\n- Short stature\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Cleft palate\n- High palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Broad forehead\n- Micrognathia\n- Hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Exotropia\n- Optic nerve hypoplasia\n- Brachydactyly\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Atrial septal defect\n- Patent foramen ovale\n- Ventriculomegaly\n- Abnormal cerebral white matter morphology\n- Downturned corners of mouth\n- Immunodeficiency\n- Short palm\n- Short stature\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Optic nerve hypoplasia\n- Restlessness\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Reduced eye contact\n- Motor delay\n- Frontal bossing\n- Sleep disturbance\n- Intestinal malrotation\n- Recurrent infections\n- Intellectual disability, severe\n- Severe global developmental delay\n- Midface retrusion\n- Central nervous system cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Optic nerve hypoplasia\n- Restlessness\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Reduced eye contact\n- Motor delay\n- Frontal bossing\n- Sleep disturbance\n- Intestinal malrotation\n- Recurrent infections\n- Intellectual disability, severe\n- Severe global developmental delay\n- Midface retrusion\n- Central nervous system cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Renal dysplasia\n- Hydronephrosis\n- Thin upper lip vermilion\n- Brachycephaly\n- Mandibular prognathia\n- Facial asymmetry\n- Narrow nose\n- Anteverted nares\n- Astigmatism\n- Ptosis\n- Hypermetropia\n- Upslanted palpebral fissure\n- Autistic behavior\n- Delayed speech and language development\n- Prominent glabella\n- Recurrent infections\n- Congenital Horner syndrome\n- Feeding difficulties in infancy\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Severe global developmental delay\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Broad forehead\n- Visual impairment\n- Apathy\n- Delayed speech and language development\n- Hyperactivity\n- Global developmental delay\n- Motor delay\n- Feeding difficulties\n- Tube feeding\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Broad forehead\n- Visual impairment\n- Apathy\n- Delayed speech and language development\n- Hyperactivity\n- Global developmental delay\n- Motor delay\n- Feeding difficulties\n- Tube feeding\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Compulsive behaviors\n- Autistic behavior\n- Inflexible adherence to routines or rituals\n- Diminished motivation\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Sleep disturbance\n- Recurrent infections\n- Episodic metabolic acidosis\n- Impaired mastication\n- Feeding difficulties\n- Overfriendliness\n- Tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Compulsive behaviors\n- Autistic behavior\n- Inflexible adherence to routines or rituals\n- Diminished motivation\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Sleep disturbance\n- Recurrent infections\n- Episodic metabolic acidosis\n- Impaired mastication\n- Feeding difficulties\n- Overfriendliness\n- Tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autistic behavior\n- Reduced eye contact\n- Global developmental delay\n- Motor delay\n- Plagiocephaly\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Prominent nasal bridge\n- Anteverted nares\n- Aggressive behavior\n- Anxiety\n- Self-mutilation\n- Delayed speech and language development\n- Motor delay\n- EEG abnormality\n- Sleep disturbance\n- Short stature\n- Impaired mastication\n- Progressive language deterioration\n- Severe global developmental delay\n- Feeding difficulties\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Prominent nasal bridge\n- Anteverted nares\n- Aggressive behavior\n- Anxiety\n- Self-mutilation\n- Delayed speech and language development\n- Motor delay\n- EEG abnormality\n- Sleep disturbance\n- Short stature\n- Impaired mastication\n- Progressive language deterioration\n- Severe global developmental delay\n- Feeding difficulties\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Epicanthus\n- Hypertelorism\n- Recurrent otitis media\n- Delayed speech and language development\n- Hyperactivity\n- Intellectual disability, mild\n- Global developmental delay\n- Obesity\n- Recurrent respiratory infections\n- High hypermetropia\n- Midface retrusion\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Obesity\n- Neonatal hypoglycemia\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Obesity\n- Neonatal hypoglycemia\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypermetropia\n- Compulsive behaviors\n- Inflexible adherence to routines or rituals\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Allergic conjunctivitis\n- Obsessive-compulsive trait\n- Impaired ability to plan\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bifid uvula\n- Microcephaly\n- Epicanthus\n- Mandibular prognathia\n- Strabismus\n- Nystagmus\n- Autistic behavior\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Constipation\n- Gastroesophageal reflux\n- Sleep disturbance\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Flat face\n- Short palpebral fissure\n- Bifid ureter\n- Central nervous system cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Malar flattening\n- Anteverted nares\n- Aggressive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Self-mutilation\n- Delayed speech and language development\n- Reduced eye contact\n- Motor delay\n- Generalized hypotonia\n- Absent speech\n- Decreased fetal movement\n- Constipation\n- Gait ataxia\n- Drooling\n- Neonatal respiratory distress\n- Sudden episodic apnea\n- Short nose\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Impaired smooth pursuit\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Posterior plagiocephaly\n- Nasogastric tube feeding in infancy\n- Brain atrophy\n- Reduced social reciprocity\n- Mild myopia\n- Physiological reactivity to cues\n- Fixated interests\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Posteriorly rotated ears\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Delayed speech and language development\n- Gynecomastia\n- Enuresis\n- Reduced eye contact\n- Jaundice\n- Tapered finger\n- Hypotonia\n- Intellectual disability, mild\n- Obesity\n- Constipation\n- Phonophobia\n- Abnormal nasal morphology\n- Metacarpophalangeal joint hyperextensibility\n- Poor fine motor coordination\n- Poor gross motor coordination\n- Repetitive compulsive behavior\n- Radial deviation of the hand or of fingers of the hand\n- Sleep apnea\n- Receptive language delay\n- Midface retrusion\n- Nuchal cord\n- Reduced social reciprocity\n- Encopresis\n- Mild microcephaly\n- Persistent preoccupation with parts of objects or unusual objects\n- Fixated interests\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Delayed speech and language development\n- Seizure\n- Intellectual disability, mild\n- EEG abnormality\n- Expressive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hearing impairment\n- Strabismus\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Intellectual disability, mild\n- Motor delay\n- Pes planus\n- Sleep disturbance\n- Attention deficit hyperactivity disorder\n- Few cafe-au-lait spots\n- Pes valgus\n- Oppositional defiant disorder\n- Frequent temper tantrums\n- Otitis media with effusion\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/01683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad forehead\n- Delayed speech and language development\n- Pes planus\n- Curly hair\n- Absent eyebrow\n- Peripheral axonal neuropathy\n- Distal amyotrophy\n- Demyelinating peripheral neuropathy\n- Pes valgus\n- Foot dorsiflexor weakness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/01684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Myopia\n- Absent eyelashes\n- Decreased nerve conduction velocity\n- Mitral valve prolapse\n- Abnormal foot morphology\n- Curly hair\n- Absent eyebrow\n- Sensory axonal neuropathy\n- Somatic sensory dysfunction\n- Motor axonal neuropathy\n- Constrictive median neuropathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/01685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Narrow forehead\n- Low-set ears\n- Short neck\n- Thickened nuchal skin fold\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Proptosis\n- Hypotonia\n- Pulmonic stenosis\n- Frontal bossing\n- Ventricular septal hypertrophy\n- Feeding difficulties\n- Tube feeding\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/01686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Narrow forehead\n- Low-set ears\n- Short neck\n- Thickened nuchal skin fold\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Proptosis\n- Hypotonia\n- Pulmonic stenosis\n- Frontal bossing\n- Ventricular septal hypertrophy\n- Feeding difficulties\n- Tube feeding\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/01687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Coarse facial features\n- Hypertelorism\n- Narrow forehead\n- Anteverted nares\n- Short neck\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Nystagmus\n- Delayed speech and language development\n- Pectus excavatum\n- Motor delay\n- Failure to thrive\n- Secundum atrial septal defect\n- Deep philtrum\n- Downturned corners of mouth\n- Short stature\n- Relative macrocephaly\n- Depressed nasal bridge\n- Severe global developmental delay\n- Feeding difficulties\n- Hepatic hemangioma\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/01688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Coarse facial features\n- Hypertelorism\n- Narrow forehead\n- Anteverted nares\n- Short neck\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Nystagmus\n- Delayed speech and language development\n- Pectus excavatum\n- Motor delay\n- Failure to thrive\n- Secundum atrial septal defect\n- Deep philtrum\n- Downturned corners of mouth\n- Short stature\n- Relative macrocephaly\n- Depressed nasal bridge\n- Severe global developmental delay\n- Feeding difficulties\n- Hepatic hemangioma\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/01689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Low-set ears\n- Webbed neck\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Hyperpigmentation of the skin\n- Cafe-au-lait spot\n- Seizure\n- Global developmental delay\n- Joint hypermobility\n- Growth delay\n- Atrial septal defect\n- Pulmonic stenosis\n- Ventricular hypertrophy\n- Deep plantar creases\n- Delayed skeletal maturation\n- Cubitus valgus\n- Short stature\n- Relative macrocephaly\n- Depressed nasal bridge\n- Deep palmar crease\n- Wide intermamillary distance\n- Thickened ears\n- Dry hair\n- Feeding difficulties\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/01690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Overfolded helix\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Thick eyebrow\n- Delayed speech and language development\n- Soft skin\n- Hemangioma\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Growth delay\n- Ventricular septal defect\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Right ventricular hypertrophy\n- Deep plantar creases\n- Neonatal hypoglycemia\n- Gastroesophageal reflux\n- Apnea\n- Short stature\n- Malnutrition\n- Deep palmar crease\n- Impaired smooth pursuit\n- Sparse hair\n- Feeding difficulties\n- Sparse eyebrow\n- Premature closure of the ductus arteriosus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/01691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent occiput\n- Mandibular prognathia\n- Short philtrum\n- Low-set ears\n- Autistic behavior\n- Tapered finger\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Hypernasal speech\n- Pes planus\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- High hypermetropia\n- Prominent forehead\n- Caesarian section\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Malar flattening\n- Mandibular prognathia\n- Nystagmus\n- Autism\n- Abnormal repetitive mannerisms\n- Seizure\n- Hypotonia\n- Motor delay\n- Specific learning disability\n- Absent speech\n- Scoliosis\n- Recurrent infections\n- Short stature\n- Decreased body weight\n- Persistence of primary teeth\n- Caesarian section\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Conductive hearing impairment\n- Sensorineural hearing impairment\n- Torticollis\n- Strabismus\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Plagiocephaly\n- Low posterior hairline\n- Localized hirsutism\n- High-pitched cry\n- Cyanotic episode\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Short philtrum\n- Delayed speech and language development\n- Sacral dimple\n- Hypotonia\n- Motor delay\n- Plagiocephaly\n- Talipes calcaneovalgus\n- Microtia\n- Uplifted earlobe\n- Ankyloglossia\n- Shoulder dimple\n- Caesarian section\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Autism\n- Tapered finger\n- Hypotonia\n- Hoarse voice\n- Aortic regurgitation\n- Short foot\n- Expressive language delay\n- Delayed skeletal maturation\n- External genital hypoplasia\n- Short stature\n- Decreased body weight\n- Lower thoracic kyphosis\n- Depressed nasal bridge\n- Short finger\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Malar flattening\n- Esotropia\n- Upslanted palpebral fissure\n- Tooth malposition\n- Aggressive behavior\n- Anxiety\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Metatarsus adductus\n- Expressive language delay\n- Clinodactyly of the 5th finger\n- Short palm\n- Low hanging columella\n- Dyslexia\n- Delayed fine motor development\n- Abnormal external nose morphology\n- Occipital cortical atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low anterior hairline\n- Autism\n- Delayed speech and language development\n- Soft skin\n- Seizure\n- Motor delay\n- Joint hypermobility\n- Mixed hypo- and hyperpigmentation of the skin\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Deeply set eye\n- Hypotelorism\n- Optic atrophy\n- Delayed speech and language development\n- Delayed puberty\n- Motor delay\n- Tremor\n- Recurrent respiratory infections\n- Hypercholesterolemia\n- Dyslexia\n- Speech apraxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Short philtrum\n- Bulbous nose\n- Strabismus\n- Deeply set eye\n- Retinal hemorrhage\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hirsutism\n- Specific learning disability\n- Scoliosis\n- Somatic sensory dysfunction\n- Short stature\n- Intermittent hyperventilation\n- Echolalia\n- Horizontal eyebrow\n- Overhanging nasal tip\n- Stereotypical body rocking\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/01700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/01701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Skin rash\n- Cutaneous photosensitivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/01702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Depressed nasal ridge\n- Cutaneous photosensitivity\n- Facial erythema\n- Broad nail\n- Patchy alopecia\n- Short stature\n- Reticulated skin pigmentation\n- Short distal phalanx of finger\n- Localized skin lesion\n- Finger swelling\n- Scaling skin\n- Sparse eyebrow\n- Telangiectasia of the skin\n- Vesicular eruption\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/01703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the dentition\n- Low-set, posteriorly rotated ears\n- Depressed nasal ridge\n- Proptosis\n- Sparse eyelashes\n- Osteopenia\n- Hyperkeratosis\n- Hypohidrosis\n- Palmoplantar hyperkeratosis\n- Cutaneous photosensitivity\n- Poikiloderma\n- Abnormality of the nail\n- High pitched voice\n- Neutropenia\n- Anemia\n- Recurrent infections\n- Slender long bone\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Abnormal blistering of the skin\n- Mixed hypo- and hyperpigmentation of the skin\n- Concave nasal ridge\n- Midface retrusion\n- Abnormal skeletal morphology\n- Thick vermilion border\n- Onychauxis\n- Epidermal acanthosis\n- Vocal cord polyp\n- Ileitis\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/01704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Underdeveloped nasal alae\n- Depressed nasal ridge\n- Proptosis\n- Sparse eyelashes\n- Hypergonadotropic hypogonadism\n- Osteopenia\n- Hypohidrosis\n- Palmoplantar hyperkeratosis\n- Cutaneous photosensitivity\n- Poikiloderma\n- High pitched voice\n- Neutropenia\n- Anemia\n- Pneumonia\n- Recurrent infections\n- Slender long bone\n- Short nose\n- Short stature\n- Agenesis of permanent teeth\n- Intermittent generalized erythematous papular rash\n- Elevated circulating follicle stimulating hormone level\n- Concave nasal ridge\n- Midface retrusion\n- Elevated circulating luteinizing hormone level\n- Onychauxis\n- Vocal cord polyp\n- Decreased serum testosterone concentration\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/01705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Carious teeth\n- Cutaneous photosensitivity\n- Poikiloderma\n- Sparse scalp hair\n- Facial telangiectasia\n- Mixed hypo- and hyperpigmentation of the skin\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/01706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Pallor\n- Agenesis of corpus callosum\n- Subsarcolemmal accumulations of abnormally shaped mitochondria\n- Autophagic vacuoles\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/01707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Cataract\n- Pallor\n- Agenesis of corpus callosum\n- Failure to thrive\n- Cardiomyopathy\n- Abnormality of the immune system\n- Abnormality of the mitochondrion\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/01708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Cataract\n- Pallor\n- Agenesis of corpus callosum\n- Failure to thrive\n- Patent foramen ovale\n- Right ventricular hypertrophy\n- Abnormality of the immune system\n- Ventricular septal hypertrophy\n- Tented upper lip vermilion\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/01709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Micrognathia\n- Proptosis\n- Platyspondyly\n- Prominent superficial veins\n- Motor delay\n- Delayed closure of the anterior fontanelle\n- Talipes equinovarus\n- Short toe\n- Coxa valga\n- Flared metaphysis\n- Fibular hypoplasia\n- Irregular vertebral endplates\n- Short stature\n- Decreased body weight\n- Overtubulated long bones\n- Short phalanx of finger\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/01710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Wide anterior fontanel\n- Micrognathia\n- Convex nasal ridge\n- Narrow nasal bridge\n- Abnormal retinal morphology\n- Cataract\n- Proptosis\n- Blue sclerae\n- Delayed speech and language development\n- Abnormal sternum morphology\n- Platyspondyly\n- Prominent superficial veins\n- Brachydactyly\n- Motor delay\n- Delayed closure of the anterior fontanelle\n- Talipes equinovarus\n- Short toe\n- Short distal phalanx of toe\n- Neutropenia\n- Spinal cord compression\n- Coxa valga\n- Platybasia\n- Osteoarthritis\n- Flared metaphysis\n- Madelung-like forearm deformities\n- Irregular vertebral endplates\n- Severe short stature\n- Decreased body weight\n- Progeroid facial appearance\n- Overtubulated long bones\n- Hypoplasia of proximal fibula\n- Hypoplastic vertebral bodies\n- Bilateral sensorineural hearing impairment\n- Pseudoepiphyses of the metacarpals\n- Low hanging columella\n- Short phalanx of finger\n- Short distal phalanx of finger\n- Short metacarpal\n- Ivory epiphyses of the phalanges of the hand\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent forehead\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/01711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureteropelvic junction obstruction\n- Hydronephrosis\n- Abnormality of the dentition\n- Hydrocephalus\n- Triangular face\n- Conductive hearing impairment\n- Cataract\n- Myopia\n- Dental crowding\n- Cupped ribs\n- Jaundice\n- Prominent scalp veins\n- Brachydactyly\n- Limited elbow extension\n- Growth delay\n- Talipes equinovarus\n- Pes planus\n- Neutropenia\n- Frontal bossing\n- Constipation\n- Recurrent aspiration pneumonia\n- Recurrent respiratory infections\n- Proportionate short stature\n- Decreased body weight\n- Premature eruption of permanent teeth\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Anisometropia\n- Recurrent streptococcal infections\n- Exophoria\n- Sparse eyebrow\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/01712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Wide nasal bridge\n- Prominent nose\n- Delayed eruption of teeth\n- Microdontia\n- Decreased response to growth hormone stimulation test\n- Acanthosis nigricans\n- Poikiloderma\n- Hip dysplasia\n- Failure to thrive\n- Scoliosis\n- Coxa vara\n- Hypoplastic iliac wing\n- Flat acetabular roof\n- Narrow pelvis bone\n- Severe short stature\n- Obtuse angle of mandible\n- Atrophy of alveolar ridges\n- Short dental root\n- Pulp obliteration\n- Intellectual disability, borderline\n- Few cafe-au-lait spots\n- Low hanging columella\n- Rootless teeth\n- Increased overbite\n- Gingival recession\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/01713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Prominent nose\n- Microdontia\n- Cutis marmorata\n- Hypoplasia of the corpus callosum\n- Hypoplastic iliac wing\n- Narrow pelvis bone\n- Severe short stature\n- Decreased body weight\n- Multiple unerupted teeth\n- Low hanging columella\n- Increased overbite\n- Clinodactyly\n- Gingival recession\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/01714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Gingivitis\n- Microcephaly\n- Micrognathia\n- Wide nasal bridge\n- Prominent nose\n- Abnormality of the incisor\n- Microdontia\n- Poikiloderma\n- Scoliosis\n- Coxa vara\n- Hypoplastic iliac wing\n- Narrow pelvis bone\n- Severe short stature\n- Decreased body weight\n- Obtuse angle of mandible\n- Atrophy of alveolar ridges\n- Short dental root\n- Pulp obliteration\n- Few cafe-au-lait spots\n- Low hanging columella\n- Mesiodens\n- Rootless teeth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/01715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Wide nasal bridge\n- Prominent nose\n- Microphthalmia\n- Delayed eruption of teeth\n- Microdontia\n- Poikiloderma\n- Intellectual disability, mild\n- Coxa valga\n- Hypoplastic iliac wing\n- Narrow pelvis bone\n- Severe short stature\n- Decreased body weight\n- Atrophy of alveolar ridges\n- Short dental root\n- Pulp obliteration\n- Thick corpus callosum\n- Few cafe-au-lait spots\n- Low hanging columella\n- Tooth agenesis\n- Increased overbite\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/01716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Wide nasal bridge\n- Prominent nose\n- Downslanted palpebral fissures\n- Microdontia\n- Poikiloderma\n- Intellectual disability, mild\n- Thrombocytosis\n- Anemia\n- Coxa valga\n- Hypoplastic iliac wing\n- Narrow pelvis bone\n- Severe short stature\n- Decreased body weight\n- Obtuse angle of mandible\n- Atrophy of alveolar ridges\n- Short dental root\n- Pulp obliteration\n- Few cafe-au-lait spots\n- Unilateral ptosis\n- Tooth agenesis\n- Rootless teeth\n- Increased overbite\n- Tapered tooth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/01717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Narrow forehead\n- Long philtrum\n- Low-set ears\n- Webbed neck\n- Short neck\n- Long eyelashes\n- Optic nerve hypoplasia\n- Hyperpigmentation of the skin\n- Hemangioma\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Hepatosplenomegaly\n- Delayed closure of the anterior fontanelle\n- Large for gestational age\n- Polyhydramnios\n- Pulmonic stenosis\n- Deep philtrum\n- Pyloric stenosis\n- Ventriculomegaly\n- Fine hair\n- Sparse hair\n- Prominent forehead\n- Myelofibrosis\n- Widened subarachnoid space\n- Tube feeding\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/01718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Dolichocephaly\n- Long philtrum\n- High forehead\n- Low-set ears\n- Astigmatism\n- Strabismus\n- Long eyelashes\n- Nystagmus\n- Abnormal sternum morphology\n- Hyperpigmentation of the skin\n- Hemangioma\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Atrial septal defect\n- Patent ductus arteriosus\n- Deep philtrum\n- Ventriculomegaly\n- Slow-growing hair\n- Short stature\n- Palmoplantar cutis laxa\n- Sparse hair\n- Widened subarachnoid space\n- Periventricular nodular heterotopia\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/01719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Low-set ears\n- Strabismus\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Hypotonia\n- Short stature\n- Decreased body weight\n- Short uvula\n- Speech apraxia\n- Moderate global developmental delay\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/01720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Pointed chin\n- Hypertelorism\n- Smooth philtrum\n- Short philtrum\n- Posteriorly rotated ears\n- Macrotia\n- Prominent nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Long eyelashes\n- Short attention span\n- Pectus excavatum of inferior sternum\n- Abnormally large globe\n- Prominent fingertip pads\n- Intellectual disability, mild\n- Small for gestational age\n- Hypernasal speech\n- Broad foot\n- Sandal gap\n- Highly arched eyebrow\n- Short palm\n- Severe muscular hypotonia\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Prominent tragus\n- Esodeviation\n- Maintenance insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/01721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Brachycephaly\n- Low anterior hairline\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Protruding ear\n- Anteverted nares\n- Ptosis\n- Long palpebral fissure\n- Synophrys\n- Oligodontia\n- Cervical ribs\n- Short tubular bones of the hand\n- Intellectual disability, mild\n- Macrodontia\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Ulnar deviation of the 2nd finger\n- Cutaneous syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/01722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Brachycephaly\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Posteriorly rotated ears\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Long palpebral fissure\n- Synophrys\n- Oligodontia\n- Global developmental delay\n- Macrodontia\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Short palm\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/01723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Brachycephaly\n- Low anterior hairline\n- Pointed chin\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Long palpebral fissure\n- Synophrys\n- Short tubular bones of the hand\n- Seizure\n- Macrodontia\n- Low posterior hairline\n- Intellectual disability, moderate\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Ulnar deviation of the 2nd finger\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/01724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Macrotia\n- Recurrent otitis media\n- Hypermetropia\n- Small for gestational age\n- Poor suck\n- Hypoplasia of the corpus callosum\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Mild global developmental delay\n- Feeding difficulties\n- Stereotypical hand wringing\n- Setting-sun eye phenomenon\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/01725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Cranial asymmetry\n- Smooth philtrum\n- Macrotia\n- Pectus excavatum\n- Thin skin\n- Growth delay\n- Small for gestational age\n- Ventricular septal defect\n- Aortic regurgitation\n- Short distal phalanx of toe\n- Ventriculomegaly\n- Delayed gross motor development\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Scoliosis\n- Kyphosis\n- Decreased body weight\n- Flat occiput\n- Focal-onset seizure\n- Broad distal phalanx of finger\n- Short distal phalanx of finger\n- Broad distal phalanx of the toes\n- Abnormal number of hair whorls\n- Intellectual disability, severe\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/01726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Micrognathia\n- Small earlobe\n- Thickened helices\n- Macrotia\n- Bulbous nose\n- Deeply set eye\n- Macrodontia of permanent maxillary central incisor\n- Inappropriate laughter\n- Delayed speech and language development\n- Hyperactivity\n- Seizure\n- Hypotonia\n- Absent speech\n- Intrauterine growth retardation\n- Small for gestational age\n- Gait ataxia\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/01727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Microdontia\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Broad nail\n- Sleep disturbance\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Tented upper lip vermilion\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Microdontia\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Broad nail\n- Sleep disturbance\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Tented upper lip vermilion\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Cleft palate\n- Coarse facial features\n- Full cheeks\n- Wide nasal bridge\n- Broad nasal tip\n- Deeply set eye\n- Autistic behavior\n- Seizure\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Decreased fetal movement\n- Broad nail\n- Abdominal pain\n- Unsteady gait\n- Intestinal malrotation\n- Elevated circulating alkaline phosphatase concentration\n- Episodic hypersomnia\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Broad nail\n- Sleep disturbance\n- Poor speech\n- Elevated circulating alkaline phosphatase concentration\n- obsolete Slowly progressive spastic quadriparesis\n- Tented upper lip vermilion\n- Brain atrophy\n- obsolete Psychomotor retardation\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Cleft palate\n- Macrocephaly\n- Ptosis\n- Abnormal repetitive mannerisms\n- Split hand\n- Hypotonia\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Absent speech\n- Plagiocephaly\n- Prenatal movement abnormality\n- Talipes\n- Dysphagia\n- Delayed gross motor development\n- Elevated circulating alkaline phosphatase concentration\n- Dysplastic corpus callosum\n- Asymmetry of the ears\n- Frontal hirsutism\n- Question mark ear\n- Hypoplastic anterior commissure\n- Aplasia of the olfactory bulb\n- Tongue thrusting\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Vesicoureteral reflux\n- Wide mouth\n- Cleft palate\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Sloping forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Proptosis\n- Exotropia\n- Optic disc coloboma\n- Long palpebral fissure\n- Dental malocclusion\n- Cafe-au-lait spot\n- Postaxial hand polydactyly\n- Hypotonia\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Bicuspid aortic valve\n- Abnormal foot morphology\n- Overlapping toe\n- Anal atresia\n- Recurrent respiratory infections\n- Exaggerated cupid's bow\n- Poor speech\n- Polyphagia\n- Downturned corners of mouth\n- Syringomyelia\n- Lumbar scoliosis\n- Deep palmar crease\n- Eversion of lateral third of lower eyelids\n- Broad lateral eyebrow\n- Mild conductive hearing impairment\n- Feeding difficulties in infancy\n- Branchial cyst\n- Dilatation of the renal pelvis\n- Severe global developmental delay\n- Pineal cyst\n- Esodeviation\n- Overweight\n- Lagophthalmos\n- Keratosis pilaris\n- Synostosis of joints\n- Thyroiditis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/01733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Vesicoureteral reflux\n- Wide mouth\n- Cleft palate\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Sloping forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Proptosis\n- Exotropia\n- Optic disc coloboma\n- Long palpebral fissure\n- Dental malocclusion\n- Cafe-au-lait spot\n- Postaxial hand polydactyly\n- Hypotonia\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Bicuspid aortic valve\n- Abnormal foot morphology\n- Overlapping toe\n- Anal atresia\n- Recurrent respiratory infections\n- Exaggerated cupid's bow\n- Poor speech\n- Polyphagia\n- Downturned corners of mouth\n- Syringomyelia\n- Lumbar scoliosis\n- Deep palmar crease\n- Eversion of lateral third of lower eyelids\n- Broad lateral eyebrow\n- Mild conductive hearing impairment\n- Feeding difficulties in infancy\n- Branchial cyst\n- Dilatation of the renal pelvis\n- Severe global developmental delay\n- Pineal cyst\n- Esodeviation\n- Overweight\n- Lagophthalmos\n- Keratosis pilaris\n- Synostosis of joints\n- Thyroiditis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/01734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Vesicoureteral reflux\n- Wide mouth\n- Cleft palate\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Sloping forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Proptosis\n- Exotropia\n- Optic disc coloboma\n- Long palpebral fissure\n- Dental malocclusion\n- Cafe-au-lait spot\n- Postaxial hand polydactyly\n- Hypotonia\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Bicuspid aortic valve\n- Abnormal foot morphology\n- Overlapping toe\n- Anal atresia\n- Recurrent respiratory infections\n- Exaggerated cupid's bow\n- Poor speech\n- Polyphagia\n- Downturned corners of mouth\n- Syringomyelia\n- Lumbar scoliosis\n- Deep palmar crease\n- Eversion of lateral third of lower eyelids\n- Broad lateral eyebrow\n- Mild conductive hearing impairment\n- Feeding difficulties in infancy\n- Branchial cyst\n- Dilatation of the renal pelvis\n- Severe global developmental delay\n- Pineal cyst\n- Esodeviation\n- Overweight\n- Lagophthalmos\n- Keratosis pilaris\n- Synostosis of joints\n- Thyroiditis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/01735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Vesicoureteral reflux\n- Wide mouth\n- Cleft palate\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Sloping forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Proptosis\n- Exotropia\n- Optic disc coloboma\n- Long palpebral fissure\n- Dental malocclusion\n- Cafe-au-lait spot\n- Postaxial hand polydactyly\n- Hypotonia\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Bicuspid aortic valve\n- Abnormal foot morphology\n- Overlapping toe\n- Anal atresia\n- Recurrent respiratory infections\n- Exaggerated cupid's bow\n- Poor speech\n- Polyphagia\n- Downturned corners of mouth\n- Syringomyelia\n- Lumbar scoliosis\n- Deep palmar crease\n- Eversion of lateral third of lower eyelids\n- Broad lateral eyebrow\n- Mild conductive hearing impairment\n- Feeding difficulties in infancy\n- Branchial cyst\n- Dilatation of the renal pelvis\n- Severe global developmental delay\n- Pineal cyst\n- Esodeviation\n- Overweight\n- Lagophthalmos\n- Keratosis pilaris\n- Synostosis of joints\n- Thyroiditis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/01736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Short lingual frenulum\n- Round face\n- Broad forehead\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Webbed neck\n- Single transverse palmar crease\n- Hyperextensible skin\n- Soft skin\n- Brachydactyly\n- Joint hypermobility\n- Bilateral ptosis\n- Growth delay\n- Umbilical hernia\n- Mitral valve prolapse\n- Bicuspid aortic valve\n- Mitral regurgitation\n- Genu recurvatum\n- Genu valgum\n- Thoracic scoliosis\n- Short long bone\n- Spinal canal stenosis\n- Shoulder dislocation\n- Clinodactyly of the 5th finger\n- Short stature\n- Increased vertebral height\n- Hypoplastic sacrum\n- Cervical C2\/C3 vertebral fusion\n- Tricuspid regurgitation\n- Almond-shaped palpebral fissure\n- Bilateral conductive hearing impairment\n- Low hanging columella\n- Limb undergrowth\n- Biventricular noncompaction cardiomyopathy\n- Fractured metatarsal bone of digit 4\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/01737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Bifid uvula\n- Retrognathia\n- Round face\n- Broad forehead\n- Long philtrum\n- Micrognathia\n- Otosclerosis\n- Low-set ears\n- Prominent nose\n- Downslanted palpebral fissures\n- Soft skin\n- Joint hypermobility\n- Bilateral ptosis\n- Dilated cardiomyopathy\n- Mitral regurgitation\n- Aortic regurgitation\n- Aortic root aneurysm\n- Coxa valga\n- Limited elbow movement\n- Spondylolisthesis\n- Easy fatigability\n- Clinodactyly of the 5th finger\n- Short stature\n- Increased vertebral height\n- Lumbar spinal canal stenosis\n- Prominent nasolabial fold\n- Abnormal atrioventricular valve morphology\n- Bilateral conductive hearing impairment\n- Low hanging columella\n- Limb undergrowth\n- Bridged palmar crease\n- Arrhythmia\n- Lower limb pain\n- Mild myopia\n- Palmar hyperlinearity\n- Thyroiditis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/01738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Long palpebral fissure\n- Nystagmus\n- Autistic behavior\n- Hypotonia\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Hepatosplenomegaly\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Large earlobe\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Patent ductus arteriosus\n- Pulmonary arterial hypertension\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Bruxism\n- Large earlobe\n- Tented upper lip vermilion\n- Protruding tongue\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Hepatosplenomegaly\n- Atrial septal defect\n- Bilateral tonic-clonic seizure\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Inverted nipples\n- Short nose\n- Large earlobe\n- Tented upper lip vermilion\n- Protruding tongue\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Optic disc pallor\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Ventriculomegaly\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Large earlobe\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Clitoral hypoplasia\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Long palpebral fissure\n- Autistic behavior\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Large earlobe\n- Tented upper lip vermilion\n- Abnormal labia minora morphology\n- Myoclonic seizure\n- Aplasia\/Hypoplasia of the clitoris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Strabismus\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Motor delay\n- Ventriculomegaly\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Large earlobe\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Severe hearing impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Cleft palate\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Strabismus\n- Long palpebral fissure\n- Dental crowding\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Bilateral tonic-clonic seizure\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Bruxism\n- Large earlobe\n- Tented upper lip vermilion\n- Anal fissure\n- Chronic constipation\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Dandy-Walker malformation\n- Plagiocephaly\n- Ventriculomegaly\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Bruxism\n- Large earlobe\n- Tented upper lip vermilion\n- Myoclonic seizure\n- Lateral ventricular asymmetry\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Strabismus\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Bruxism\n- High hypermetropia\n- Large earlobe\n- Tented upper lip vermilion\n- Generalized myoclonic-tonic-clonic seizure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Narrow mouth\n- Micrognathia\n- Talipes equinovarus\n- Abnormality of tibia morphology\n- Aplasia\/Hypoplasia of fingers\n- Agenesis of mandibular central incisor\n- Clinodactyly\n- Abnormal radial ray morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/01748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micrognathia\n- Pectus excavatum\n- Abnormality of the larynx\n- Abnormal foot morphology\n- Abnormality of tibia morphology\n- Short finger\n- Short thumb\n- Abnormal radial ray morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/01749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Malar flattening\n- Short philtrum\n- Macrotia\n- Prominent nasal bridge\n- Abnormal nasal tip morphology\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Aggressive behavior\n- Anxiety\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Sandal gap\n- Constipation\n- Inverted nipples\n- Prominent metopic ridge\n- Single interphalangeal crease of fifth finger\n- Skin-picking\n- Flat face\n- Encopresis\n- Arachnoid cyst\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/01750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Abnormality of the urinary system\n- Horseshoe kidney\n- Abnormality of the genitourinary system\n- High palate\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Ptosis\n- Blepharophimosis\n- Amblyopia\n- Enuresis\n- Sacral dimple\n- Intellectual disability\n- Growth delay\n- Highly arched eyebrow\n- Skull asymmetry\n- Recurrent infections\n- Radioulnar synostosis\n- Limited elbow movement\n- Short stature\n- Moderate sensorineural hearing impairment\n- Deviated nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/01751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the urinary system\n- Horseshoe kidney\n- Hypertelorism\n- Triangular face\n- Abnormal pinna morphology\n- Sacral dimple\n- Intellectual disability\n- Global developmental delay\n- Growth delay\n- Umbilical hernia\n- Frontal bossing\n- Highly arched eyebrow\n- Skull asymmetry\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/01752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the urinary system\n- Hydronephrosis\n- Broad forehead\n- Posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Blepharophimosis\n- Amblyopia\n- Enuresis\n- Sacral dimple\n- Intellectual disability\n- Global developmental delay\n- Growth delay\n- Umbilical hernia\n- Highly arched eyebrow\n- Short stature\n- Decreased body weight\n- Preauricular pit\n- Premature loss of primary teeth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/01753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Hypermetropia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Joint laxity\n- Disproportionate tall stature\n- Vomiting\n- Gastroesophageal reflux\n- Sleep disturbance\n- Hyperextensibility of the knee\n- Overfriendliness\n- Early satiety\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Nystagmus\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Seizure\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Joint laxity\n- Cerebral atrophy\n- Ventriculomegaly\n- Developmental regression\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Abnormal hippocampus morphology\n- Periventricular white matter hyperintensities\n- Overfriendliness\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Anxiety\n- Global developmental delay\n- Generalized-onset seizure\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Short philtrum\n- Low-set ears\n- Narrow nose\n- Deeply set eye\n- Autism\n- Aggressive behavior\n- Anxiety\n- Single transverse palmar crease\n- Dry skin\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Intellectual disability, moderate\n- Long nose\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Microtia\n- Dry hair\n- Chronic fatigue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Prominent fingertip pads\n- Hypotonia\n- Motor delay\n- Joint laxity\n- Pes planus\n- Thrombocytopenia\n- Intellectual disability, moderate\n- Kyphosis\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Pes valgus\n- Speech apraxia\n- Moderate global developmental delay\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Prominent nose\n- Abnormal repetitive mannerisms\n- Anxiety\n- Inappropriate laughter\n- Seizure\n- Global developmental delay\n- Dystonia\n- Short foot\n- Bilateral tonic-clonic seizure\n- Apnea\n- Sleep disturbance\n- Developmental regression\n- Scoliosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Intermittent hyperventilation\n- Intellectual disability, severe\n- Myoclonic absence seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Broad nasal tip\n- Abnormal repetitive mannerisms\n- Anxiety\n- Seizure\n- Global developmental delay\n- Atrial septal defect\n- Patent ductus arteriosus\n- Intellectual disability, moderate\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Abnormality of the chin\n- Bulbous nose\n- Strabismus\n- Hypermetropia\n- Autism\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Slender finger\n- Seizure\n- Global developmental delay\n- Constipation\n- Sleep disturbance\n- Bruxism\n- Attention deficit hyperactivity disorder\n- Few cafe-au-lait spots\n- Abnormal columella morphology\n- Intellectual disability, severe\n- Midface retrusion\n- Pica\n- Hair-pulling\n- Self-injurious behavior\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Short philtrum\n- Underdeveloped nasal alae\n- Deeply set eye\n- Autism\n- Abnormal repetitive mannerisms\n- Anxiety\n- Hypothyroidism\n- Hirsutism\n- Acne\n- Slender finger\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Disproportionate tall stature\n- Decreased fetal movement\n- Pes planus\n- Intellectual disability, moderate\n- EEG abnormality\n- Sleep disturbance\n- Developmental regression\n- Episodic vomiting\n- Scoliosis\n- Hyperventilation\n- Impaired pain sensation\n- Peripheral visual field loss\n- Sleep apnea\n- Increased serum testosterone level\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Short philtrum\n- Macrotia\n- Diastema\n- Abnormal repetitive mannerisms\n- Dry skin\n- Prominent fingertip pads\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Dystonia\n- Joint laxity\n- Drooling\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Abnormal columella morphology\n- Multifocal epileptiform discharges\n- EEG with multifocal slow activity\n- Intellectual disability, severe\n- Myoclonic absence seizure\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Anxiety\n- Intellectual disability, moderate\n- Delayed myelination\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Abnormal repetitive mannerisms\n- Purpura\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Developmental regression\n- Intellectual disability, severe\n- Continuous spike and waves during slow sleep\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/01765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Myopia\n- Autism\n- Seizure\n- Absent speech\n- Plagiocephaly\n- Gait imbalance\n- Sleep disturbance\n- Highly arched eyebrow\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n- Thick nasal alae\n- Broad hallux\n- Severe global developmental delay\n- Thick vermilion border\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/01766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Smooth philtrum\n- Short philtrum\n- Downslanted palpebral fissures\n- Periorbital fullness\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Short nose\n- Sparse lateral eyebrow\n- Frequent temper tantrums\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/01767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n- Hip dysplasia\n- Frontal bossing\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Speech articulation difficulties\n- Infra-orbital crease\n- Recurrent ear infections\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/01768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Open mouth\n- Coarse facial features\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Autism\n- Reduced eye contact\n- Prominent fingertip pads\n- Hypotonia\n- Absent speech\n- Plagiocephaly\n- Small nail\n- Short distal phalanx of toe\n- Ventriculomegaly\n- Gait imbalance\n- Depressed nasal bridge\n- Focal-onset seizure\n- Edema of the dorsum of hands\n- Increased adipose tissue\n- Short distal phalanx of finger\n- Everted upper lip vermilion\n- Severe global developmental delay\n- Brain atrophy\n- Thick vermilion border\n- Wide nasal ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/01769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, mild\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/01770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Anteverted nares\n- Telecanthus\n- Hypotonia\n- Global developmental delay\n- Short columella\n- Vomiting\n- Diarrhea\n- Hypoplasia of the corpus callosum\n- Fine hair\n- Slow-growing hair\n- Short nose\n- Tented upper lip vermilion\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/01771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Long eyelashes\n- Edema\n- Hypotonia\n- Myoclonus\n- Absent speech\n- Large for gestational age\n- Short toe\n- Bilateral tonic-clonic seizure\n- Depressed nasal bridge\n- Broad phalanx\n- Edema of the dorsum of hands\n- Short phalanx of finger\n- Severe global developmental delay\n- Delayed myelination\n- Thick vermilion border\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/01772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Triangular face\n- Intellectual disability\n- Global developmental delay\n- Constipation\n- Abnormality of neuronal migration\n- Poor speech\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/01773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Abnormality of the outer ear\n- Low-set ears\n- Depressed nasal ridge\n- Short neck\n- Downslanted palpebral fissures\n- Autistic behavior\n- Hypotonia\n- Absent speech\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/01774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocephalus\n- Retrognathia\n- Hearing impairment\n- Strabismus\n- Epicanthus inversus\n- Absent speech\n- Polyhydramnios\n- Ventricular septal defect\n- Ventriculomegaly\n- Tracheobronchomalacia\n- Multiple joint contractures\n- Short stature\n- Decreased body weight\n- Tricuspid regurgitation\n- Periventricular leukomalacia\n- Stridor\n- Severe global developmental delay\n- Retractile testis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/01775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Deeply set eye\n- Proptosis\n- Dental malocclusion\n- Anxiety\n- Intellectual disability, mild\n- Motor delay\n- Hypernasal speech\n- Exaggerated cupid's bow\n- Sleep disturbance\n- Scoliosis\n- Enamel hypomineralization\n- Enamel hypoplasia\n- Prominent floating ribs\n- Axial hypotonia\n- Chin with vertical crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Downslanted palpebral fissures\n- Global developmental delay\n- Delayed closure of the anterior fontanelle\n- Abnormality of connective tissue\n- Excessive wrinkled skin\n- Metopic depression\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/01777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Coarse facial features\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Atypical behavior\n- Pterygium\n- Seizure\n- Joint laxity\n- Delayed closure of the anterior fontanelle\n- Pneumothorax\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Excessive wrinkled skin\n- Joint subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/01778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Hypertelorism\n- Prominent supraorbital ridges\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Sleep disturbance\n- Developmental regression\n- Abnormality of the gastrointestinal tract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Hypertelorism\n- Prominent supraorbital ridges\n- Downslanted palpebral fissures\n- Autistic behavior\n- Anxiety\n- Seizure\n- Sleep disturbance\n- Abnormality of the gastrointestinal tract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Prominent supraorbital ridges\n- Autistic behavior\n- Anxiety\n- Intellectual disability\n- Seizure\n- Pes planus\n- Sleep disturbance\n- Abnormality of the gastrointestinal tract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Prominent supraorbital ridges\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Developmental regression\n- Abnormality of the gastrointestinal tract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Prominent supraorbital ridges\n- Downslanted palpebral fissures\n- Intellectual disability\n- Abnormality of the gastrointestinal tract\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/01783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Tall stature\n- Polycystic ovaries\n- Macrocephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Pointed chin\n- Downslanted palpebral fissures\n- Aggressive behavior\n- Delayed speech and language development\n- Irregular menstruation\n- Hirsutism\n- Large hands\n- Hypotonia\n- Joint laxity\n- Polyphagia\n- Accelerated skeletal maturation\n- High anterior hairline\n- Prominent forehead\n- Abnormal temper tantrums\n- Overweight\n- Long fingers\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/01784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Long face\n- Pointed chin\n- Astigmatism\n- Downslanted palpebral fissures\n- Atypical behavior\n- Impaired social interactions\n- Delayed speech and language development\n- Hirsutism\n- Numerous nevi\n- Accelerated skeletal maturation\n- Slowed slurred speech\n- Overweight\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/01785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Sensorineural hearing impairment\n- Strabismus\n- Visual impairment\n- Spasticity\n- Motor delay\n- Dystonia\n- Absent speech\n- Hyperreflexia\n- Hip dysplasia\n- Bilateral tonic-clonic seizure\n- Developmental regression\n- EEG with focal spikes\n- Delayed myelination\n- Recurrent gastroenteritis\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/01786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Macrocephaly\n- Pointed chin\n- Triangular face\n- Short chin\n- Narrow forehead\n- Deeply set eye\n- Autism\n- Delayed speech and language development\n- Hyperactivity\n- Large hands\n- Intellectual disability\n- Megalencephaly\n- Large for gestational age\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/01787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Open mouth\n- Macrocephaly\n- Hypertelorism\n- Smooth philtrum\n- Strabismus\n- Hyperpigmentation of the skin\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Large for gestational age\n- Neonatal hypoglycemia\n- Large forehead\n- Ventriculomegaly\n- Gliosis\n- Venous malformation\n- Distributed along Blaschko lines\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/01788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Smooth philtrum\n- Posteriorly rotated ears\n- Delayed speech and language development\n- Hypotonia\n- Large for gestational age\n- Bilateral talipes equinovarus\n- Ventriculomegaly\n- Delayed skeletal maturation\n- Reduced subcutaneous adipose tissue\n- Progressive macrocephaly\n- Intellectual disability, severe\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/01789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic male external genitalia\n- High palate\n- Autistic behavior\n- Nephrolithiasis\n- Tapered finger\n- Hypotonia\n- Motor delay\n- Absent speech\n- Joint laxity\n- Pes planus\n- Constipation\n- Broad-based gait\n- EEG abnormality\n- Focal impaired awareness seizure\n- Scoliosis\n- Genu valgum\n- Inverted nipples\n- Short stature\n- Intellectual disability, severe\n- Feeding difficulties\n- Delayed myelination\n- Overweight\n- Tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Delayed speech and language development\n- Soft skin\n- Hypotonia\n- Motor delay\n- Pes planus\n- Dysphagia\n- Broad-based gait\n- Intellectual disability, moderate\n- Short stature\n- Intellectual disability, severe\n- Feeding difficulties\n- Delayed myelination\n- Overweight\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Protruding ear\n- Strabismus\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Tapered finger\n- Hypotonia\n- Motor delay\n- Absent speech\n- Pes planus\n- Dysphagia\n- Apnea\n- Broad-based gait\n- Hyperbilirubinemia\n- Mild short stature\n- Central hypoventilation\n- Almond-shaped palpebral fissure\n- High hypermetropia\n- High anterior hairline\n- Intellectual disability, severe\n- Feeding difficulties\n- Delayed myelination\n- Decreased serum iron\n- Low levels of vitamin D\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Facial hypotonia\n- Strabismus\n- Ptosis\n- Nystagmus\n- Abnormal repetitive mannerisms\n- Delayed puberty\n- Soft skin\n- Tapered finger\n- Seizure\n- Ataxia\n- Hypotonia\n- Motor delay\n- Absent speech\n- Hip dysplasia\n- Joint laxity\n- Pes planus\n- Short foot\n- Dysphagia\n- Constipation\n- Apnea\n- Broad-based gait\n- Exaggerated startle response\n- EEG abnormality\n- Scoliosis\n- Abnormal pattern of respiration\n- Short palm\n- Decreased skull ossification\n- Temperature instability\n- Feeding difficulties in infancy\n- Broad columella\n- Intellectual disability, severe\n- Delayed myelination\n- Decreased hemoglobin concentration\n- Tube feeding\n- Low levels of vitamin D\n- Cerebral visual impairment\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Tapered finger\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Constipation\n- Apnea\n- Abnormal pattern of respiration\n- Babinski sign\n- Short palm\n- Temperature instability\n- Congenital megaureter\n- Feeding difficulties in infancy\n- Tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypermetropia\n- Nystagmus\n- Abnormality of visual evoked potentials\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Hip dysplasia\n- Joint laxity\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Exaggerated startle response\n- EEG abnormality\n- Abnormal cerebral white matter morphology\n- Abnormal pattern of respiration\n- Short palm\n- Temperature instability\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Dysphagia\n- Gastroesophageal reflux\n- Generalized non-motor (absence) seizure\n- Abnormal pattern of respiration\n- Temperature instability\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Strabismus\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Pes planus\n- Dysphagia\n- EEG abnormality\n- Sleep disturbance\n- Scoliosis\n- Abnormal pattern of respiration\n- Deep palmar crease\n- Stooped posture\n- Abnormal muscle fiber-type distribution\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Downslanted palpebral fissures\n- Telecanthus\n- Nystagmus\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Dysphagia\n- Constipation\n- Generalized non-motor (absence) seizure\n- Recurrent lower respiratory tract infections\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Frequent temper tantrums\n- Tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Abnormality of refraction\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Ventricular septal defect\n- Dysphagia\n- Exaggerated startle response\n- Unsteady gait\n- EEG abnormality\n- Hypercholesterolemia\n- High anterior hairline\n- Delayed myelination\n- Short palpebral fissure\n- Motor regression\n- Low levels of vitamin D\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Eczema\n- Soft skin\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Joint laxity\n- Pes planus\n- Dysphagia\n- Constipation\n- Exaggerated startle response\n- EEG abnormality\n- Abnormal pattern of respiration\n- Temperature instability\n- Focal-onset seizure\n- Feeding difficulties in infancy\n- Abnormality of the palmar creases\n- Intellectual disability, severe\n- Self-biting\n- Hooded eyelid\n- Motor regression\n- Tube feeding\n- obsolete Toe walking\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Facial hypotonia\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Tremor\n- Absent speech\n- Exaggerated startle response\n- Hyperbilirubinemia\n- Almond-shaped palpebral fissure\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Facial hypotonia\n- Protruding ear\n- Strabismus\n- Delayed speech and language development\n- Prominent fingertip pads\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Hip dysplasia\n- Dysphagia\n- Constipation\n- Bilateral tonic-clonic seizure\n- Apnea\n- Ventriculomegaly\n- Generalized non-motor (absence) seizure\n- EEG abnormality\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Limb hypertonia\n- Scoliosis\n- Abnormal pattern of respiration\n- Mild short stature\n- Temperature instability\n- Almond-shaped palpebral fissure\n- Feeding difficulties in infancy\n- High anterior hairline\n- Long toe\n- Atonic seizure\n- Intellectual disability, severe\n- Unilateral cryptorchidism\n- Tube feeding\n- Cerebral visual impairment\n- Hypersomnia\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Delayed speech and language development\n- Seizure\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Absent speech\n- Hip dysplasia\n- Patent ductus arteriosus\n- Short foot\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- EEG abnormality\n- Scoliosis\n- Abnormal pattern of respiration\n- Short palm\n- Short stature\n- Temperature instability\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Overweight\n- Tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Protruding ear\n- Atypical behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Short foot\n- Status epilepticus\n- Intellectual disability, moderate\n- Increased variability in muscle fiber diameter\n- Short palm\n- Almond-shaped palpebral fissure\n- Feeding difficulties in infancy\n- Leg muscle stiffness\n- High anterior hairline\n- EEG with temporal sharp waves\n- Generalized atonic seizure\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypotonia\n- Neonatal hypotonia\n- Intellectual disability, moderate\n- EEG abnormality\n- Elevated circulating thyroid-stimulating hormone concentration\n- Almond-shaped palpebral fissure\n- High anterior hairline\n- Myoclonic seizure\n- Low levels of vitamin D\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Facial hypotonia\n- Delayed speech and language development\n- Soft skin\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Joint laxity\n- Pes planus\n- Dysphagia\n- Broad-based gait\n- Intellectual disability, moderate\n- Coxa valga\n- Decreased body weight\n- High anterior hairline\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Uterine prolapse\n- High palate\n- Epicanthus\n- Facial hypotonia\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Jaundice\n- Soft skin\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Joint laxity\n- Pes planus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Broad-based gait\n- Generalized-onset seizure\n- Exaggerated startle response\n- Drooling\n- Intellectual disability, moderate\n- EEG abnormality\n- Abnormal pattern of respiration\n- Depressed nasal bridge\n- Temperature instability\n- Almond-shaped palpebral fissure\n- Feeding difficulties in infancy\n- Premature thelarche\n- Intellectual disability, severe\n- Hyperplastic labia majora\n- Hooded eyelid\n- Motor regression\n- Tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Anteverted nares\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Motor delay\n- Dysphagia\n- Gastroesophageal reflux\n- Exaggerated startle response\n- Drooling\n- Depressed nasal bridge\n- Apneic episodes in infancy\n- Feeding difficulties in infancy\n- Abnormality of movement\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/01808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Trigonocephaly\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Coloboma\n- Short attention span\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Pachygyria\n- Broad nail\n- Ventriculomegaly\n- Highly arched eyebrow\n- Short stature\n- Thick corpus callosum\n- Congenital ptosis\n- Microtia\n- Dilation of Virchow-Robin spaces\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/01809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureterocele\n- Vesicoureteral reflux\n- Long face\n- Retrognathia\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Bulbous nose\n- Abnormal nasal bridge morphology\n- Prominent nasal bridge\n- Wide nasal bridge\n- Anteverted nares\n- Thick eyebrow\n- Synophrys\n- Growth delay\n- Macrodontia\n- Hypernasal speech\n- Abnormal facial shape\n- Frontal bossing\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Atrioventricular canal defect\n- Short metacarpal\n- Caesarian section\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/01810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureterocele\n- Long face\n- Retrognathia\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Bulbous nose\n- Abnormal nasal bridge morphology\n- Prominent nasal bridge\n- Wide nasal bridge\n- Anteverted nares\n- Thick eyebrow\n- Growth delay\n- Macrodontia\n- Hypernasal speech\n- Abnormal facial shape\n- Frontal bossing\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Atrioventricular canal defect\n- Short metacarpal\n- Caesarian section\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/01811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Full cheeks\n- Hypertelorism\n- Hearing impairment\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Long palpebral fissure\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Cerebellar vermis hypoplasia\n- Small nail\n- Ventriculomegaly\n- Elevated circulating alkaline phosphatase concentration\n- Decreased body weight\n- Depressed nasal bridge\n- Shortening of all distal phalanges of the fingers\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Midface retrusion\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/01812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Narrow forehead\n- Micrognathia\n- Anteverted nares\n- Strabismus\n- Ptosis\n- Short nose\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/01813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Narrow forehead\n- Micrognathia\n- Anteverted nares\n- Strabismus\n- Ptosis\n- Short nose\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/01814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Narrow forehead\n- Micrognathia\n- Anteverted nares\n- Strabismus\n- Ptosis\n- Short nose\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/01815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Oligodontia\n- Single transverse palmar crease\n- Brachydactyly\n- Intellectual disability, mild\n- Hypernasal speech\n- Small nail\n- Short distal phalanx of toe\n- Scoliosis\n- Short nose\n- Short stature\n- Decreased body weight\n- Short third metatarsal\n- Short fourth metatarsal\n- Midface retrusion\n- Feeding difficulties\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent nose\n- Narrow nose\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- High forehead\n- Hearing impairment\n- Strabismus\n- Downslanted palpebral fissures\n- Telecanthus\n- Proptosis\n- Oligodontia\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Craniosynostosis\n- Hypernasal speech\n- Overlapping toe\n- Short distal phalanx of toe\n- Chiari malformation\n- Short nose\n- Short third metatarsal\n- Short fourth metatarsal\n- Short fifth metatarsal\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent nose\n- Narrow nose\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Hypertelorism\n- High forehead\n- Broad nasal tip\n- Short neck\n- Strabismus\n- Motor delay\n- Craniosynostosis\n- Short nose\n- Coronal craniosynostosis\n- 2-3 toe syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Osteoporosis\n- Hemangioma\n- Seizure\n- Hypotonia\n- Motor delay\n- Hypertonia\n- Absent speech\n- Chiari malformation\n- Intellectual disability, moderate\n- Sleep disturbance\n- Inability to walk\n- Short nose\n- Short stature\n- Decreased body weight\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent nose\n- Narrow nose\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Broad nasal tip\n- Short neck\n- Strabismus\n- Retinopathy\n- Deeply set eye\n- Hypermetropia\n- Nystagmus\n- Abnormal repetitive mannerisms\n- Brachydactyly\n- Hypotonia\n- Motor delay\n- Absent speech\n- Overlapping toe\n- Intellectual disability, moderate\n- Inability to walk\n- Short nose\n- Severe short stature\n- Decreased body weight\n- Intellectual disability, severe\n- Delayed myelination\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Strabismus\n- Hypermetropia\n- Blepharophimosis\n- Autistic behavior\n- Brachydactyly\n- Motor delay\n- Absent speech\n- Intellectual disability, moderate\n- Congenital bilateral hip dislocation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Short philtrum\n- Broad nasal tip\n- Strabismus\n- Deeply set eye\n- Blepharophimosis\n- Hypotelorism\n- Autistic behavior\n- Brachydactyly\n- Hypotonia\n- Motor delay\n- Absent speech\n- Overlapping toe\n- Intellectual disability, moderate\n- Short nose\n- Short stature\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Strabismus\n- Hypermetropia\n- Blepharophimosis\n- Autistic behavior\n- Brachydactyly\n- Motor delay\n- Absent speech\n- Intellectual disability, moderate\n- Congenital bilateral hip dislocation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Shawl scrotum\n- Thick lower lip vermilion\n- Long face\n- Epicanthus\n- Short philtrum\n- Posteriorly rotated ears\n- Broad nasal tip\n- Strabismus\n- Retinopathy\n- Deeply set eye\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Hypotelorism\n- Photophobia\n- Nystagmus\n- Optic atrophy\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Seizure\n- Hypotonia\n- Motor delay\n- Absent speech\n- Flexion contracture\n- Joint laxity\n- Pes planus\n- Constipation\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Intellectual disability, severe\n- Cerebral white matter hypoplasia\n- Transient neutropenia\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Shawl scrotum\n- Thick lower lip vermilion\n- Long face\n- Epicanthus\n- Short philtrum\n- Posteriorly rotated ears\n- Broad nasal tip\n- Strabismus\n- Retinopathy\n- Deeply set eye\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Hypotelorism\n- Photophobia\n- Nystagmus\n- Optic atrophy\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Seizure\n- Hypotonia\n- Motor delay\n- Absent speech\n- Flexion contracture\n- Joint laxity\n- Pes planus\n- Constipation\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Intellectual disability, severe\n- Cerebral white matter hypoplasia\n- Transient neutropenia\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Epicanthus\n- High forehead\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Intellectual disability, mild\n- Motor delay\n- Overlapping toe\n- Sleep disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Short philtrum\n- High forehead\n- Broad nasal tip\n- Strabismus\n- Deeply set eye\n- Hypotelorism\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Motor delay\n- Absent speech\n- Intellectual disability, moderate\n- Severe short stature\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Broad nasal tip\n- Astigmatism\n- Deeply set eye\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Sandal gap\n- Intellectual disability, moderate\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Strabismus\n- Retinopathy\n- Deeply set eye\n- Telecanthus\n- Hypermetropia\n- Autistic behavior\n- Nevus flammeus\n- Brachydactyly\n- Hypotonia\n- Motor delay\n- Absent speech\n- Umbilical hernia\n- Constipation\n- Intellectual disability, moderate\n- Severe short stature\n- Decreased body weight\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Shawl scrotum\n- Cleft palate\n- Thick lower lip vermilion\n- Microcephaly\n- Long face\n- Epicanthus\n- Short philtrum\n- Broad nasal tip\n- Deeply set eye\n- Blepharophimosis\n- Adducted thumb\n- Seizure\n- Motor delay\n- Absent speech\n- Overlapping toe\n- Intellectual disability, profound\n- Severe short stature\n- Decreased body weight\n- Short thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Microcephaly\n- Long face\n- Epicanthus\n- Short philtrum\n- High forehead\n- Broad nasal tip\n- Deeply set eye\n- Blepharophimosis\n- Abnormal repetitive mannerisms\n- Tapered finger\n- Hypotonia\n- Motor delay\n- Absent speech\n- Intellectual disability, moderate\n- Scoliosis\n- Short nose\n- Short stature\n- Progressive flexion contractures\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Hearing impairment\n- Broad nasal tip\n- Strabismus\n- Retinopathy\n- Deeply set eye\n- Blepharophimosis\n- Brachydactyly\n- Hypotonia\n- Motor delay\n- Absent speech\n- Flexion contracture\n- Anteriorly placed anus\n- Overlapping toe\n- Constipation\n- Intellectual disability, profound\n- Patellar dislocation\n- Short stature\n- Decreased body weight\n- Preauricular pit\n- High hypermetropia\n- Congenital bilateral hip dislocation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Hearing impairment\n- Broad nasal tip\n- Strabismus\n- Retinopathy\n- Deeply set eye\n- Blepharophimosis\n- Brachydactyly\n- Hypotonia\n- Motor delay\n- Absent speech\n- Flexion contracture\n- Anteriorly placed anus\n- Overlapping toe\n- Constipation\n- Intellectual disability, profound\n- Patellar dislocation\n- Short stature\n- Decreased body weight\n- Preauricular pit\n- High hypermetropia\n- Congenital bilateral hip dislocation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- High forehead\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Strabismus\n- Deeply set eye\n- Blepharophimosis\n- Hypotelorism\n- Nystagmus\n- Dental crowding\n- Abnormal repetitive mannerisms\n- Motor delay\n- Absent speech\n- Overlapping toe\n- Intellectual disability, profound\n- Severe short stature\n- Curved fingers\n- Decreased body weight\n- Impaired pain sensation\n- High hypermetropia\n- Clitoral hypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Epicanthus\n- High forehead\n- Broad nasal tip\n- Deeply set eye\n- Blepharophimosis\n- Hypotelorism\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Intellectual disability, moderate\n- Sleep disturbance\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Epicanthus\n- High forehead\n- Broad nasal tip\n- Deeply set eye\n- Blepharophimosis\n- Hypotelorism\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Intellectual disability, moderate\n- Sleep disturbance\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Shawl scrotum\n- Thin upper lip vermilion\n- Long face\n- Epicanthus\n- Short philtrum\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Hypermetropia\n- Blepharophimosis\n- Delayed speech and language development\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Motor delay\n- Flexion contracture\n- Short nail\n- Overlapping toe\n- Constipation\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Short stature\n- Decreased body weight\n- Lower limb hypertonia\n- Pes valgus\n- obsolete Infantile hypercalcemia\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Shawl scrotum\n- Thin upper lip vermilion\n- Long face\n- Epicanthus\n- Short philtrum\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Hypermetropia\n- Blepharophimosis\n- Delayed speech and language development\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Motor delay\n- Flexion contracture\n- Short nail\n- Overlapping toe\n- Constipation\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Short stature\n- Decreased body weight\n- Lower limb hypertonia\n- Pes valgus\n- obsolete Infantile hypercalcemia\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/01843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Micrognathia\n- Proptosis\n- Thin skin\n- Prominent scalp veins\n- Joint stiffness\n- Freckling\n- Failure to thrive\n- Growth delay\n- Alopecia\n- Hypoplastic toenails\n- Absent eyebrow\n- Kyphosis\n- Easy fatigability\n- Minimal subcutaneous fat\n- Reduced bone mineral density\n- Persistent open anterior fontanelle\n- Craniofacial disproportion\n- Excessive wrinkled skin\n- Exercise-induced leg cramps\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Circumoral cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/01844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Micrognathia\n- Absent earlobe\n- Convex nasal ridge\n- Triangular nasal tip\n- Narrow nose\n- Proptosis\n- Abnormal thorax morphology\n- Thin skin\n- Hypopigmentation of the skin\n- Prominent scalp veins\n- Thickened skin\n- Hemiparesis\n- High pitched voice\n- Abnormal myocardium morphology\n- Hemolytic anemia\n- Broad-based gait\n- Sparse scalp hair\n- Alopecia of scalp\n- Shuffling gait\n- Wormian bones\n- Hyperbilirubinemia\n- Enlarged joints\n- Limb muscle weakness\n- Minimal subcutaneous fat\n- Reduced bone mineral density\n- Poor appetite\n- Craniofacial disproportion\n- Thin calvarium\n- Erythroid hyperplasia\n- Cephalohematoma\n- Rete ridge flattening\n- Abnormal nasal cartilage morphology\n- Systolic heart murmur\n- Sparse eyebrow\n- Abnormality of movement\n- Facial cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/01845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glossoptosis\n- Cleft palate\n- Long philtrum\n- Micrognathia\n- Pectus excavatum\n- Brachydactyly\n- Patent foramen ovale\n- Sandal gap\n- Gastroesophageal reflux\n- Short stature\n- Decreased body weight\n- Deep palmar crease\n- Short 5th finger\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Cleft palate\n- Bifid uvula\n- High palate\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Synophrys\n- Abnormally large globe\n- Specific learning disability\n- Cholesteatoma\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft soft palate\n- Facial hemangioma\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Hypotonia\n- Hyporeflexia\n- Hip dysplasia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Lacrimal duct stenosis\n- Feeding difficulties\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pectus carinatum\n- Failure to thrive\n- Sandal gap\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Short stature\n- Spondylolisthesis at L5-S1\n- Short proximal phalanx of the 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Obstructive sleep apnea\n- Short nose\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Brachydactyly\n- Short nose\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Anteverted nares\n- Pectus excavatum\n- Failure to thrive\n- Ventricular septal defect\n- Wolff-Parkinson-White syndrome\n- Pleural effusion\n- Obstructive sleep apnea\n- Short nose\n- Single interphalangeal crease of fifth finger\n- Short 5th finger\n- Chylothorax\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pierre-Robin sequence\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Short nose\n- Short stature\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- High palate\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Thickened cortex of long bones\n- Short nose\n- Short stature\n- Lumbar scoliosis\n- Short 5th metacarpal\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/01855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Large fontanelles\n- Retrognathia\n- Hypertelorism\n- Short chin\n- Long philtrum\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Proptosis\n- Blue sclerae\n- Long palpebral fissure\n- Brachydactyly\n- Small for gestational age\n- Patent ductus arteriosus\n- Frontal bossing\n- Hypoplasia of the radius\n- Hypoplasia of the ulna\n- Short long bone\n- Mesomelia\n- Short nose\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Deep palmar crease\n- Wide intermamillary distance\n- Nail dystrophy\n- Upper limb undergrowth\n- Broad hallux\n- Short uvula\n- Midface retrusion\n- Clinodactyly of the 2nd finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Polycystic ovaries\n- Triangular mouth\n- Gingival overgrowth\n- Epicanthus\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Wide nasal bridge\n- Anteverted nares\n- Telecanthus\n- Developmental cataract\n- Proptosis\n- Blue sclerae\n- Abnormal sternum morphology\n- Brachydactyly\n- Ventricular septal defect\n- Scoliosis\n- Mesomelia\n- Short nose\n- Short stature\n- Premature ovarian insufficiency\n- Tooth agenesis\n- Bifid tongue\n- Midface retrusion\n- Clinodactyly\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypertelorism\n- Micrognathia\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Upslanted palpebral fissure\n- Brachydactyly\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Frontal bossing\n- Bilateral cleft lip and palate\n- Mesomelia\n- Short nose\n- Short middle phalanx of the 5th finger\n- Short stature\n- Tricuspid regurgitation\n- Depressed nasal bridge\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Clitoral hypoplasia\n- Vesicoureteral reflux\n- Cleft palate\n- Gingival overgrowth\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Upslanted palpebral fissure\n- Blue sclerae\n- Abnormal sternum morphology\n- Sacral dimple\n- Brachydactyly\n- Syndactyly\n- Omphalocele\n- Ventricular septal defect\n- Bifid distal phalanx of toe\n- Mesomelia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Abnormality of dental morphology\n- Short phalanx of finger\n- Duplication of the distal phalanx of hand\n- Broad hallux\n- Bifid tongue\n- Pulmonary valve atresia\n- Hypoplastic right heart\n- Broad thumb\n- Midface retrusion\n- Camptodactyly\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Macrocephaly\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Webbed neck\n- Telecanthus\n- Upslanted palpebral fissure\n- Brachydactyly\n- Umbilical hernia\n- Sandal gap\n- Frontal bossing\n- Downturned corners of mouth\n- Mesomelia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Tooth agenesis\n- Broad hallux\n- Bifid tongue\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypospadias\n- Abnormality of the dentition\n- Cleft soft palate\n- Gingival overgrowth\n- Macrocephaly\n- Wide anterior fontanel\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Proptosis\n- Upslanted palpebral fissure\n- Blue sclerae\n- Abnormal sternum morphology\n- Platyspondyly\n- Sacral dimple\n- Brachydactyly\n- Hip dysplasia\n- Small nail\n- Frontal bossing\n- Kyphoscoliosis\n- Mesomelia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the uvula\n- Hypoplasia of the anterior nasal spine\n- Increased bone mineral density\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Gingival overgrowth\n- Thin vermilion border\n- Hypertelorism\n- Broad forehead\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Brachydactyly\n- Micromelia\n- Clinodactyly of the 5th finger\n- Short stature\n- Relative macrocephaly\n- Broad hallux\n- Bifid tongue\n- Broad thumb\n- Midface retrusion\n- Hypoplastic female external genitalia\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Gingival overgrowth\n- Thin vermilion border\n- Hypertelorism\n- Broad forehead\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Brachydactyly\n- Mesomelia\n- Clinodactyly of the 5th finger\n- Short thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Gingival overgrowth\n- Thin vermilion border\n- Hypertelorism\n- Broad forehead\n- Low-set ears\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Brachydactyly\n- Mesomelia\n- External genital hypoplasia\n- Mild short stature\n- Broad hallux\n- Bifid tongue\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/01864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Round face\n- Hypertelorism\n- Abnormality of the eye\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Motor delay\n- Absent speech\n- Failure to thrive\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Round face\n- Hypertelorism\n- Abnormality of the eye\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Motor delay\n- Absent speech\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Round face\n- Hypertelorism\n- Abnormality of the eye\n- Atypical behavior\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Seizure\n- Motor delay\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Round face\n- Hypertelorism\n- Abnormality of the eye\n- Atypical behavior\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Motor delay\n- Absent speech\n- Failure to thrive\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Round face\n- Hypertelorism\n- Atypical behavior\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Motor delay\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Round face\n- Hypertelorism\n- Abnormality of the eye\n- Delayed speech and language development\n- Motor delay\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/01870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Male hypogonadism\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n- Gastroesophageal reflux\n- Sleep disturbance\n- Short stature\n- Attention deficit hyperactivity disorder\n- Sleep apnea\n- Feeding difficulties\n- Skin-picking\n- Chronic constipation\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n- Failure to thrive\n- Short foot\n- Gastroesophageal reflux\n- Poor suck\n- Kyphoscoliosis\n- Multiple joint contractures\n- Short palm\n- Short stature\n- Attention deficit hyperactivity disorder\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Asthma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Abnormality of the eye\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Short foot\n- Poor suck\n- Multiple joint contractures\n- Short palm\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Kyphoscoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Autistic behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Neonatal hypotonia\n- Absent speech\n- Hip dysplasia\n- Gastroesophageal reflux\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Atypical behavior\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Neonatal hypotonia\n- Failure to thrive\n- Decreased fetal movement\n- Gastroesophageal reflux\n- Chronic diarrhea\n- Sleep disturbance\n- Sleep apnea\n- Skin-picking\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Absent speech\n- Hip dysplasia\n- Failure to thrive\n- Short foot\n- Gastroesophageal reflux\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Atypical behavior\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Absent speech\n- Failure to thrive\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Global developmental delay\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Atypical behavior\n- Delayed speech and language development\n- Global developmental delay\n- Asthma\n- Sleep disturbance\n- Kyphoscoliosis\n- Increased body weight\n- Sleep apnea\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Atypical behavior\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Asthma\n- Sleep disturbance\n- Kyphoscoliosis\n- Increased body weight\n- Sleep apnea\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/01882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Optic atrophy\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Infantile spasms\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Optic atrophy\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Global developmental delay\n- Febrile seizure (within the age range of 3 months to 6 years)\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Optic atrophy\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Optic atrophy\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Optic atrophy\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Attention deficit hyperactivity disorder\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Global developmental delay\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Optic atrophy\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Optic atrophy\n- Autistic behavior\n- Intellectual disability\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/01893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Shawl scrotum\n- Hypertelorism\n- Long philtrum\n- Abnormality of the outer ear\n- Anteverted nares\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Pectus excavatum\n- Broad palm\n- Broad foot\n- Frontal bossing\n- Delayed skeletal maturation\n- Short nose\n- Short palm\n- Short stature\n- Exostoses\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/01894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Shawl scrotum\n- Hypertelorism\n- Abnormality of the outer ear\n- Preauricular skin tag\n- Anteverted nares\n- Single transverse palmar crease\n- Broad palm\n- Global developmental delay\n- Obesity\n- Delayed skeletal maturation\n- Short nose\n- Short palm\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/01895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypospadias\n- Shawl scrotum\n- Micropenis\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- Abnormality of the outer ear\n- Anteverted nares\n- Ptosis\n- Broad palm\n- Global developmental delay\n- Obesity\n- Umbilical hernia\n- Short nose\n- Mild short stature\n- Short palm\n- Short 5th finger\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/01896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/01897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Central diabetes insipidus\n- Partial agenesis of the corpus callosum\n- Growth delay\n- Lobar holoprosencephaly\n- Mild global developmental delay\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/01898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Central diabetes insipidus\n- Partial agenesis of the corpus callosum\n- Growth delay\n- Intellectual disability, moderate\n- Semilobar holoprosencephaly\n- Bilateral cleft lip and palate\n- Synostosis involving the 3rd metacarpal\n- Moderate global developmental delay\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/01899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Facial asymmetry\n- Abnormality of the inner ear\n- Hearing impairment\n- Bicornuate uterus\n- Cryptophthalmos\n- Laryngeal stenosis\n- Laryngeal web\n- Stridor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/01900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Underdeveloped nasal alae\n- Anophthalmia\n- Cryptophthalmos\n- Seizure\n- Agenesis of corpus callosum\n- Craniosynostosis\n- Laryngeal stenosis\n- Abnormal cortical gyration\n- Bilateral cleft lip and palate\n- Short stature\n- Decreased body weight\n- Preauricular pit\n- Laryngeal web\n- Abnormality of the palpebral fissures\n- Microtia\n- Aplasia\/Hypoplasia involving the nose\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/01901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Underdeveloped nasal alae\n- Narrow nose\n- Microcornea\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/01902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/01903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Underdeveloped nasal alae\n- Narrow nose\n- Microcornea\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/01904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Underdeveloped nasal alae\n- Narrow nose\n- Microcornea\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/01905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Depressed nasal tip\n- Broad nasal tip\n- Strabismus\n- Long eyelashes\n- Long palpebral fissure\n- Dental malocclusion\n- Atypical behavior\n- Hirsutism\n- Prominent fingertip pads\n- Hypotonia\n- Joint laxity\n- Atrial septal defect\n- Neonatal hypoglycemia\n- Short columella\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Short stature\n- Eversion of lateral third of lower eyelids\n- Feeding difficulties in infancy\n- Severe global developmental delay\n- Areolar fullness\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Protruding ear\n- Broad nasal tip\n- Strabismus\n- Long eyelashes\n- Long palpebral fissure\n- Atypical behavior\n- Hirsutism\n- Prominent fingertip pads\n- Joint laxity\n- Coarctation of aorta\n- Short stature\n- Decreased body weight\n- Sparse lateral eyebrow\n- Mild global developmental delay\n- Areolar fullness\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Cupped ear\n- Protruding ear\n- Depressed nasal tip\n- Broad nasal tip\n- Long eyelashes\n- Long palpebral fissure\n- Dental malocclusion\n- Hirsutism\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability, mild\n- Joint laxity\n- Neonatal hypoglycemia\n- Short columella\n- Highly arched eyebrow\n- Short stature\n- Decreased body weight\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n- Feeding difficulties in infancy\n- Moderate global developmental delay\n- Areolar fullness\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- High palate\n- Protruding ear\n- Depressed nasal tip\n- Long eyelashes\n- Long palpebral fissure\n- Brachydactyly\n- Prominent fingertip pads\n- Seizure\n- Global developmental delay\n- Joint laxity\n- Pulmonic stenosis\n- Right ventricular outlet tract obstruction\n- Highly arched eyebrow\n- Short stature\n- Decreased body weight\n- Hypoplasia of right ventricle\n- Atrioventricular canal defect\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- High palate\n- Thin upper lip vermilion\n- Short chin\n- Long palpebral fissure\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Joint laxity\n- Atrial septal defect\n- Pulmonic stenosis\n- Gastroesophageal reflux\n- Hypsarrhythmia\n- Downturned corners of mouth\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Protruding ear\n- Depressed nasal tip\n- Broad nasal tip\n- Long palpebral fissure\n- Highly arched eyebrow\n- Eversion of lateral third of lower eyelids\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Protruding ear\n- Depressed nasal tip\n- Broad nasal tip\n- Long palpebral fissure\n- Oligodontia\n- Sparse lateral eyebrow\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Chorioretinal coloboma\n- Iris coloboma\n- Hypotonia\n- Ventricular septal defect\n- Aortic valve stenosis\n- Coarctation of aorta\n- Subvalvular aortic stenosis\n- Hypoplastic left heart\n- Feeding difficulties in infancy\n- Double tooth\n- Mild global developmental delay\n- Labial adhesion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/01915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Short chin\n- Prominent supraorbital ridges\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Wrist flexion contracture\n- Broad finger\n- Fused cervical vertebrae\n- Dislocated radial head\n- Pes valgus\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/01916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Short chin\n- Prominent supraorbital ridges\n- Hearing impairment\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Wrist flexion contracture\n- Broad finger\n- Scoliosis\n- Flared metaphysis\n- Dislocated radial head\n- Undermodelled hand bones\n- Keloids\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/01917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Short chin\n- Prominent supraorbital ridges\n- Hearing impairment\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Wrist flexion contracture\n- Broad finger\n- Scoliosis\n- Flared metaphysis\n- Dislocated radial head\n- Undermodelled hand bones\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/01918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microglossia\n- Cleft palate\n- High palate\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Ptosis\n- Motor delay\n- Growth delay\n- Pulmonary arterial hypertension\n- Scoliosis\n- Congenital contracture\n- Myopathy\n- Pectoralis hypoplasia\n- Hypoplasia of the musculature\n- Feeding difficulties\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/01919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Ptosis\n- Motor delay\n- Growth delay\n- Congenital contracture\n- Hypoplasia of the musculature\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/01920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Ptosis\n- Motor delay\n- Growth delay\n- Talipes\n- Myopathy\n- Elevated circulating creatine kinase concentration\n- Pectoralis hypoplasia\n- Hypoplasia of the musculature\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/01921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Motor delay\n- Growth delay\n- Scoliosis\n- Elevated circulating creatine kinase concentration\n- Hypoplasia of the musculature\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/01922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microglossia\n- High palate\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Ptosis\n- Motor delay\n- Growth delay\n- Pectoralis hypoplasia\n- Hypoplasia of the musculature\n- Joint contracture of the 5th finger\n- Joint contracture of the 4th finger\n- Feeding difficulties\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/01923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Ptosis\n- Motor delay\n- Scoliosis\n- Myopathy\n- Elevated circulating creatine kinase concentration\n- Pectoralis hypoplasia\n- Hypoplasia of the musculature\n- Joint contracture of the 5th finger\n- Joint contracture of the 4th finger\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/01924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Pointed chin\n- Triangular face\n- Oligodontia\n- Widely spaced teeth\n- Osteopenia\n- Overlapping toe\n- Highly arched eyebrow\n- Scoliosis\n- Vertebral compression fracture\n- 2-3 toe syndactyly\n- Multiple rib fractures\n- Poor gross motor coordination\n- Midface retrusion\n- Esodeviation\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/01925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Epicanthus\n- Broad forehead\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Pear-shaped nose\n- Upslanted palpebral fissure\n- Delayed eruption of teeth\n- Atypical behavior\n- Dry skin\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Failure to thrive\n- Intrauterine growth retardation\n- Pes planus\n- Deep philtrum\n- Intellectual disability, moderate\n- Scoliosis\n- Hip dislocation\n- Abnormality of hair texture\n- Broad chin\n- Feeding difficulties\n- Laryngospasm\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/01926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Chronic otitis media\n- Bulbous nose\n- Wide nose\n- Ptosis\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Intrauterine growth retardation\n- Small for gestational age\n- Laryngomalacia\n- Atrial septal defect\n- Patent foramen ovale\n- Poor suck\n- Bilateral tonic-clonic seizure\n- Recurrent upper respiratory tract infections\n- Inverted nipples\n- Short stature\n- Deep palmar crease\n- Feeding difficulties\n- Short palpebral fissure\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/01927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Epicanthus\n- Mandibular prognathia\n- Hypertelorism\n- High forehead\n- Low-set ears\n- Protruding ear\n- Bulbous nose\n- Wide nose\n- Anteverted nares\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Pectus excavatum\n- Narrow chest\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Slender build\n- Asymmetry of the thorax\n- Pes planus\n- Poor suck\n- Microtia\n- Broad columella\n- Tented upper lip vermilion\n- Broad chin\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/01928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Long face\n- Epicanthus\n- Smooth philtrum\n- Bulbous nose\n- Pear-shaped nose\n- Webbed neck\n- Short neck\n- Telecanthus\n- Upslanted palpebral fissure\n- Microdontia\n- Sacral dimple\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Abnormal foot morphology\n- Pes planus\n- Fair hair\n- Short stature\n- Stridor\n- Broad chin\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/01929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Open mouth\n- Long face\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- High forehead\n- Recurrent otitis media\n- Prominent nasal bridge\n- Wide nose\n- Pear-shaped nose\n- Hypermetropia\n- Upslanted palpebral fissure\n- Single transverse palmar crease\n- Sacral dimple\n- Numerous nevi\n- Global developmental delay\n- Neonatal hypotonia\n- Joint laxity\n- Ventricular septal defect\n- Pes planus\n- Unsteady gait\n- Scoliosis\n- Bilateral cleft lip and palate\n- Inspiratory stridor\n- Feeding difficulties in infancy\n- Short palpebral fissure\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/01930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Brachycephaly\n- Retrognathia\n- Micrognathia\n- High forehead\n- Posteriorly rotated ears\n- Oligodontia\n- Widely spaced teeth\n- Thin ribs\n- Osteopenia\n- Tapered finger\n- Motor delay\n- Growth delay\n- Bell-shaped thorax\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Multiple rib fractures\n- Bilateral conductive hearing impairment\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/01931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Posteriorly rotated ears\n- Blue sclerae\n- Narrow chest\n- Patent foramen ovale\n- Highly arched eyebrow\n- Decreased body weight\n- Multiple prenatal fractures\n- Poor gross motor coordination\n- Rhizomelia\n- Tented upper lip vermilion\n- Midface retrusion\n- Left-to-right shunt\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/01932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Duplicated collecting system\n- High palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Square face\n- Long philtrum\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Abnormality of the middle ear\n- Depressed nasal tip\n- Abnormality of the eye\n- Visual impairment\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Umbilical hernia\n- Patent ductus arteriosus\n- Aortic regurgitation\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Recurrent upper respiratory tract infections\n- Hip dislocation\n- Thoracolumbar scoliosis\n- Patellar dislocation\n- Short stature\n- B Acute Lymphoblastic Leukemia\n- Depressed nasal bridge\n- Abnormality of dental eruption\n- Lacrimal duct stenosis\n- Distributed along Blaschko lines\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nephrocalcinosis\n- Hydronephrosis\n- Hypertelorism\n- Widow's peak\n- Posteriorly rotated ears\n- Recurrent otitis media\n- Conductive hearing impairment\n- Wide nasal bridge\n- Choanal atresia\n- Delayed speech and language development\n- Sacral dimple\n- Hypertrichosis\n- Postaxial hand polydactyly\n- Hypotonia\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Joint laxity\n- Atrial septal defect\n- Rocker bottom foot\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Hypoplastic nipples\n- Short stature\n- Abnormal thyroid-stimulating hormone level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Macrocephaly\n- Wide anterior fontanel\n- Long face\n- Smooth philtrum\n- Recurrent otitis media\n- Choanal atresia\n- Strabismus\n- Deeply set eye\n- Delayed speech and language development\n- Hypothyroidism\n- Hyperpigmentation of the skin\n- Hypertrichosis\n- Postaxial hand polydactyly\n- Tapered finger\n- Intellectual disability, mild\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Joint hypermobility\n- Anteriorly placed anus\n- Pes cavus\n- Hypoplasia of the corpus callosum\n- Thoracic kyphosis\n- Retrocerebellar cyst\n- Asymmetry of the breasts\n- Distributed along Blaschko lines\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Large fontanelles\n- Narrow face\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypothyroidism\n- Intellectual disability\n- Seizure\n- Motor delay\n- Dandy-Walker malformation\n- Ventriculomegaly\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Scoliosis\n- Areas of hypopigmentation and hyperpigmentation that do not follow Blaschko lines\n- Broad lateral eyebrow\n- Prominent forehead\n- Distributed along Blaschko lines\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin upper lip vermilion\n- Pointed chin\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Ptosis\n- Dental crowding\n- Aggressive behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Pectus excavatum\n- Sacral dimple\n- Intellectual disability\n- Motor delay\n- Dandy-Walker malformation\n- Hip dysplasia\n- Failure to thrive\n- Pes planus\n- Low posterior hairline\n- Sleep disturbance\n- Scoliosis\n- Genu valgum\n- Short stature\n- Prominent nasolabial fold\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Delayed speech and language development\n- Motor delay\n- Generalized hypotonia\n- Joint hypermobility\n- Hip dysplasia\n- Short stature\n- Prominent forehead\n- Nasogastric tube feeding in infancy\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Hearing impairment\n- Choanal atresia\n- Abnormality of the eye\n- Abnormal dental enamel morphology\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Anteriorly placed anus\n- Abnormal heart morphology\n- Ventriculomegaly\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- No permanent dentition\n- Distributed along Blaschko lines\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Abnormality of the dentition\n- Delayed speech and language development\n- Hypothyroidism\n- Intellectual disability\n- Motor delay\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Distributed along Blaschko lines\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Bifid uvula\n- Widow's peak\n- Posteriorly rotated ears\n- Hearing impairment\n- Recurrent otitis media\n- Wide nasal bridge\n- Depressed nasal tip\n- Choanal stenosis\n- Choanal atresia\n- Abnormality of the eye\n- Strabismus\n- Myopia\n- Delayed speech and language development\n- Sacral dimple\n- Hypertrichosis\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Dandy-Walker malformation\n- Cerebellar hypoplasia\n- Anteriorly placed anus\n- Abnormal heart morphology\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Highly arched eyebrow\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Short stature\n- Aplasia\/Hypoplasia of the cerebellar vermis\n- Distributed along Blaschko lines\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Micrognathia\n- Hearing impairment\n- Bulbous nose\n- Torticollis\n- Hypotelorism\n- Delayed speech and language development\n- Narrow chest\n- Abnormality of skin pigmentation\n- Intellectual disability, mild\n- Motor delay\n- Congenital hip dislocation\n- Joint hypermobility\n- Prominent nasolabial fold\n- Abnormality of dental eruption\n- Patellar aplasia\n- Down-sloping shoulders\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Rectovaginal fistula\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Facial asymmetry\n- Low-set ears\n- Recurrent otitis media\n- Conductive hearing impairment\n- Bulbous nose\n- Wide nasal bridge\n- Choanal atresia\n- Cataract\n- Delayed speech and language development\n- Short clavicles\n- Single transverse palmar crease\n- Sacral dimple\n- Motor delay\n- Dandy-Walker malformation\n- Polyhydramnios\n- Ventriculomegaly\n- Scoliosis\n- Osteosarcoma\n- Short palpebral fissure\n- Distributed along Blaschko lines\n- Postaxial polydactyly\n- Lower limb asymmetry\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Narrow forehead\n- Low-set ears\n- Sensorineural hearing impairment\n- Bulbous nose\n- Choanal atresia\n- Hypermetropia\n- Hypodontia\n- Delayed speech and language development\n- Short clavicles\n- Single umbilical artery\n- Intellectual disability\n- Motor delay\n- Hip dysplasia\n- Absent axillary hair\n- Scoliosis\n- Short stature\n- Short palpebral fissure\n- Distributed along Blaschko lines\n- Abnormal breast morphology\n- Postaxial polydactyly\n- Lower limb asymmetry\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- High palate\n- Mandibular prognathia\n- Broad forehead\n- High forehead\n- Posteriorly rotated ears\n- Low-set ears\n- Small earlobe\n- Overfolded helix\n- Conductive hearing impairment\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Depressed nasal tip\n- Periorbital fullness\n- Short sternum\n- Brachydactyly\n- Global developmental delay\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Brisk reflexes\n- Intrauterine growth retardation\n- Hypernasal speech\n- Patent ductus arteriosus\n- Pes planus\n- Short toe\n- Short columella\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Generalized non-motor (absence) seizure\n- Enlarged cisterna magna\n- Abnormal cortical gyration\n- Depressed nasal bridge\n- 2-5 finger cutaneous syndactyly\n- 2-3 toe cutaneous syndactyly\n- Wide intermamillary distance\n- Retrocerebellar cyst\n- Focal-onset seizure\n- Narrow naris\n- Prominent calcaneus\n- Short palpebral fissure\n- Postaxial polydactyly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Ptosis\n- Hypotelorism\n- Delayed speech and language development\n- Shield chest\n- Single transverse palmar crease\n- Hirsutism\n- Hypotonia\n- Motor delay\n- Joint laxity\n- Pes planus\n- Achilles tendon contracture\n- Short toe\n- Sandal gap\n- Anal atresia\n- Recurrent respiratory infections\n- Intellectual disability, moderate\n- Short palm\n- Short stature\n- Anal fistula\n- Mesiodens\n- Distributed along Blaschko lines\n- Narrow palpebral fissure\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/01946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Broad forehead\n- High forehead\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/01947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Full cheeks\n- Round face\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Anteverted nares\n- Esotropia\n- Upslanted palpebral fissure\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Shield chest\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Talipes equinovarus\n- Hepatomegaly\n- Obstructive sleep apnea\n- Relative macrocephaly\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Retrocerebellar cyst\n- Simplified gyral pattern\n- Tented upper lip vermilion\n- Horizontal eyebrow\n- Feeding difficulties\n- Clinodactyly\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/01948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Chronic otitis media\n- Protruding ear\n- Bulbous nose\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Obstructive sleep apnea\n- Depressed nasal bridge\n- Simplified gyral pattern\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/01949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Anteverted nares\n- Hypermetropia\n- Esotropia\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Excessive daytime somnolence\n- Global developmental delay\n- Short toe\n- Constipation\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Scoliosis\n- Tracheomalacia\n- Short palm\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Focal-onset seizure\n- Uplifted earlobe\n- Tented upper lip vermilion\n- Horizontal eyebrow\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/01950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Anteverted nares\n- Hypermetropia\n- Esotropia\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Excessive daytime somnolence\n- Global developmental delay\n- Short toe\n- Constipation\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Scoliosis\n- Tracheomalacia\n- Short palm\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Focal-onset seizure\n- Uplifted earlobe\n- Tented upper lip vermilion\n- Horizontal eyebrow\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/01951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Round face\n- Hypertelorism\n- Narrow forehead\n- Thickened helices\n- Wide nasal bridge\n- Ptosis\n- Upslanted palpebral fissure\n- Macrodontia of permanent maxillary central incisor\n- Widely spaced teeth\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Joint hypermobility\n- Polyhydramnios\n- Short foot\n- Metatarsus adductus\n- Toe clinodactyly\n- Constipation\n- Delayed gross motor development\n- Frontal upsweep of hair\n- Exaggerated cupid's bow\n- Sparse lateral eyebrow\n- Delayed fine motor development\n- Broad eyebrow\n- Flat face\n- Premature adrenarche\n- Hooded eyelid\n- Hyperintensity of cerebral white matter on MRI\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/01952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Dolichocephaly\n- Hypertelorism\n- Micrognathia\n- Bulbous nose\n- Wide nasal bridge\n- Blepharophimosis\n- Synophrys\n- Delayed speech and language development\n- Bruising susceptibility\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Frontal bossing\n- Apraxia\n- Exaggerated cupid's bow\n- EEG abnormality\n- Cubitus valgus\n- Nevus\n- 2-3 toe syndactyly\n- Esophageal ulceration\n- Feeding difficulties in infancy\n- Narrow naris\n- Abnormal hair whorl\n- Overjet\n- Horizontal eyebrow\n- Flat face\n- Overweight\n- Narrow palpebral fissure\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/01953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Round face\n- Hypertelorism\n- Wide nasal bridge\n- Ptosis\n- Blepharophimosis\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Joint hypermobility\n- Generalized non-motor (absence) seizure\n- Abnormal spinal cord morphology\n- Delayed gross motor development\n- Delayed fine motor development\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/01954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Round face\n- Hypertelorism\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Ptosis\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Joint hypermobility\n- Delayed gross motor development\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/01955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Low anterior hairline\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Widely spaced teeth\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Delayed gross motor development\n- Premature thelarche\n- Delayed fine motor development\n- Flat face\n- Cerebral white matter hypoplasia\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/01956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Round face\n- Hypertelorism\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Ptosis\n- Blepharophimosis\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Pulmonic stenosis\n- Delayed gross motor development\n- Feeding difficulties in infancy\n- Abnormality of the palmar creases\n- Flat face\n- Thick vermilion border\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/01957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Micrognathia\n- Posteriorly rotated ears\n- Underdeveloped nasal alae\n- Convex nasal ridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Microphthalmia\n- Entropion\n- Trichiasis\n- Failure to thrive\n- Laryngomalacia\n- Frontal bossing\n- Gastroesophageal reflux\n- Delayed skeletal maturation\n- Tracheomalacia\n- Short stature\n- Decreased body weight\n- Patellar aplasia\n- Microtia\n- Feeding difficulties in infancy\n- Abnormal reproductive system morphology\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micrognathia\n- High forehead\n- Underdeveloped nasal alae\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Failure to thrive\n- Emphysema\n- Delayed skeletal maturation\n- Lumbar hyperlordosis\n- Short stature\n- Decreased body weight\n- Patellar aplasia\n- Microtia\n- Urethral stenosis\n- Feeding difficulties in infancy\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Everted lower lip vermilion\n- Microcephaly\n- Micrognathia\n- High forehead\n- Posteriorly rotated ears\n- Underdeveloped nasal alae\n- Convex nasal ridge\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Lumbar hyperlordosis\n- Short stature\n- Patellar aplasia\n- Microtia\n- Feeding difficulties in infancy\n- Thick vermilion border\n- Sparse medial eyebrow\n- Hip subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/01961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/01962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Pointed chin\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/01963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Low-set ears\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/01964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long philtrum\n- Chronic otitis media\n- Anteverted nares\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/01965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Facial hypotonia\n- Reduced eye contact\n- Hypotonia\n- Muscle weakness\n- Short foot\n- Constipation\n- Bilateral tonic-clonic seizure\n- Inability to walk\n- Obstructive sleep apnea\n- Short palm\n- Intellectual disability, severe\n- Severe global developmental delay\n- Feeding difficulties\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/01966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Facial hypotonia\n- Alternating esotropia\n- Hypotonia\n- Constipation\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Inability to walk\n- Short stature\n- Multifocal epileptiform discharges\n- Intellectual disability, severe\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/01967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Esotropia\n- Hypotonia\n- Muscle weakness\n- Absent speech\n- Short foot\n- Constipation\n- Bilateral tonic-clonic seizure\n- Scoliosis\n- Abnormality of thyroid physiology\n- Short palm\n- Short stature\n- Atypical absence seizure\n- Atonic seizure\n- EEG with spike-wave complexes\n- Intellectual disability, severe\n- Severe global developmental delay\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/01968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hearing impairment\n- Blue sclerae\n- Autism\n- Pectus carinatum\n- Hypothyroidism\n- Periorbital hyperpigmentation\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Limited elbow extension\n- Growth delay\n- Abnormal heart morphology\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Gait imbalance\n- Brittle hair\n- 4-5 toe syndactyly\n- Vascular ring\n- Cleft anterior mitral valve leaflet\n- Double aortic arch\n- Clinodactyly\n- Abnormality of movement\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/01969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Cleft palate\n- Abnormal oral frenulum morphology\n- Microcephaly\n- Hearing impairment\n- Otitis media\n- Torticollis\n- Upslanted palpebral fissure\n- Blue sclerae\n- Synophrys\n- Pectus excavatum\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Joint laxity\n- Growth delay\n- Anteriorly placed anus\n- Rotary nystagmus\n- Abnormal heart morphology\n- Gastroesophageal reflux\n- Lower limb spasticity\n- Recurrent aspiration pneumonia\n- Gait imbalance\n- Downturned corners of mouth\n- Kyphoscoliosis\n- 4-5 toe syndactyly\n- Ankyloglossia\n- Vascular ring\n- Double aortic arch\n- Clinodactyly\n- Abnormality of movement\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/01970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Esotropia\n- Intellectual disability\n- Gait imbalance\n- Sleep disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/01971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Open mouth\n- Microcephaly\n- Smooth philtrum\n- Short philtrum\n- Chronic otitis media\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Nasolacrimal duct obstruction\n- Intellectual disability\n- Ataxia\n- Dysphagia\n- Gait imbalance\n- Sleep disturbance\n- Kyphoscoliosis\n- Short stature\n- Decreased body weight\n- Lower limb hypertonia\n- Clinodactyly\n- Abnormality of movement\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/01972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Delayed gross motor development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Delayed gross motor development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Hypotelorism\n- Thickened skin\n- Brachydactyly\n- Delayed skeletal maturation\n- Short stature\n- Depressed nasal bridge\n- Midface retrusion\n- Thick vermilion border\n- Stiff finger\n- Internal notch of the femoral head\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Hypotelorism\n- Thickened skin\n- Brachydactyly\n- Delayed skeletal maturation\n- Short stature\n- Depressed nasal bridge\n- Midface retrusion\n- Thick vermilion border\n- Stiff finger\n- Internal notch of the femoral head\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Hypotelorism\n- Thickened skin\n- Brachydactyly\n- Delayed skeletal maturation\n- Short stature\n- Depressed nasal bridge\n- Midface retrusion\n- Thick vermilion border\n- Stiff finger\n- Internal notch of the femoral head\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Hypotelorism\n- Thickened skin\n- Brachydactyly\n- Delayed skeletal maturation\n- Short stature\n- Depressed nasal bridge\n- Midface retrusion\n- Thick vermilion border\n- Stiff finger\n- Internal notch of the femoral head\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Thick eyebrow\n- Synophrys\n- Delayed eruption of teeth\n- Seizure\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Dandy-Walker malformation\n- Cerebellar hypoplasia\n- Deep philtrum\n- Large forehead\n- Frontal bossing\n- Increased intracranial pressure\n- Recurrent infections\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Thick nasal alae\n- Intellectual disability, severe\n- Feeding difficulties\n- Narrow palpebral fissure\n- Testicular torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Thick eyebrow\n- Synophrys\n- Delayed eruption of teeth\n- Seizure\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Dandy-Walker malformation\n- Cerebellar hypoplasia\n- Deep philtrum\n- Large forehead\n- Frontal bossing\n- Increased intracranial pressure\n- Recurrent infections\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Thick nasal alae\n- Intellectual disability, severe\n- Feeding difficulties\n- Narrow palpebral fissure\n- Testicular torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Thickened skin\n- Short stature\n- Depressed nasal bridge\n- Midface retrusion\n- Thick vermilion border\n- Stiff finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Thickened skin\n- Short stature\n- Depressed nasal bridge\n- Midface retrusion\n- Thick vermilion border\n- Stiff finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Anteriorly placed anus\n- Bicoronal synostosis\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Periorbital fullness\n- Atypical behavior\n- Hypotonia\n- Umbilical hernia\n- Deep philtrum\n- Large forehead\n- Frontal bossing\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Thick nasal alae\n- Short metacarpal\n- Short metatarsal\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Bowing of the legs\n- Short stature\n- Decreased body weight\n- Aplasia\/Hypoplasia of the patella\n- Microtia\n- Anorectal anomaly\n- Thin eyebrow\n- Copper beaten skull\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Periorbital fullness\n- Atypical behavior\n- Hypotonia\n- Umbilical hernia\n- Deep philtrum\n- Large forehead\n- Frontal bossing\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Thick nasal alae\n- Short metacarpal\n- Short metatarsal\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/01986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Hypotelorism\n- Thickened skin\n- Short stature\n- Acromelia\n- Midface retrusion\n- Stiff finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Round face\n- Bulbous nose\n- Wide nasal bridge\n- Hypotelorism\n- Thickened skin\n- Short stature\n- Acromelia\n- Midface retrusion\n- Stiff finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Low-set ears\n- Proptosis\n- Anteriorly placed anus\n- Ventricular septal defect\n- Short stature\n- Decreased body weight\n- Microtia\n- Mild conductive hearing impairment\n- Bicoronal synostosis\n- Bilambdoid synostosis\n- Thin eyebrow\n- Duodenal stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micropenis\n- High palate\n- Aplasia\/Hypoplasia of the patella\n- Microtia\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Decreased body weight\n- Widely patent sagittal suture\n- Abnormality of the metopic suture\n- Microtia\n- Bicoronal synostosis\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hearing impairment\n- Aplasia\/Hypoplasia of the patella\n- Microtia\n- Bicoronal synostosis\n- Heart block\n- Thin eyebrow\n- Breast aplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/01993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Joint stiffness\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short foot\n- Hepatomegaly\n- J-shaped sella turcica\n- Lumbar hyperlordosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Cone-shaped epiphysis\n- Midface retrusion\n- Thick vermilion border\n- Limited shoulder flexion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/01999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Round face\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Abnormality of the vertebral column\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Hyperreflexia\n- Obesity\n- Patent ductus arteriosus\n- Splenomegaly\n- Constipation\n- Pulmonary arterial hypertension\n- Asthma\n- Coarse hair\n- Short stature\n- Chronic lung disease\n- Sleep apnea\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/02000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Short toe\n- Short stature\n- Disproportionate short-limb short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/02001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Short toe\n- Short stature\n- Disproportionate short-limb short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/02002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Bulbous nose\n- Wide nasal bridge\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short stature\n- Relative macrocephaly\n- Short chordae tendineae of the mitral valve\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/02003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Bulbous nose\n- Wide nasal bridge\n- Abnormal mitral valve morphology\n- Mitral regurgitation\n- Short stature\n- Relative macrocephaly\n- Short chordae tendineae of the mitral valve\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/02004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long face\n- Short chin\n- High forehead\n- Low-set, posteriorly rotated ears\n- Prominent nasal bridge\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Motor delay\n- Small for gestational age\n- Deep philtrum\n- Horizontal eyebrow\n- Broad chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/02005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Long face\n- Short chin\n- High forehead\n- Small earlobe\n- Prominent nasal bridge\n- Strabismus\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability\n- Dysarthria\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Thin nail\n- Deep philtrum\n- Gastroesophageal reflux\n- Attention deficit hyperactivity disorder\n- Horizontal eyebrow\n- Broad chin\n- Increased femoral anteversion\n- Thick vermilion border\n- Eosinophilic infiltration of the esophagus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/02006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Increased body weight\n- Depressed nasal bridge\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/02007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High forehead\n- Strabismus\n- Long eyelashes\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Ataxia\n- Motor delay\n- Deep philtrum\n- Relative macrocephaly\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/02008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Smooth philtrum\n- High forehead\n- Prominent nasal bridge\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Dimple chin\n- Broad chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/02009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Low-set ears\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Phimosis\n- Bilateral talipes equinovarus\n- Constipation\n- Axial hypotonia\n- Thin lower lip vermilion\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/02010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- Widow's peak\n- Thick eyebrow\n- Delayed speech and language development\n- Joint laxity\n- Unilateral ptosis\n- Abnormality of the hairline\n- Dilatation of the renal pelvis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- Widow's peak\n- Thick eyebrow\n- Delayed speech and language development\n- Joint laxity\n- Unilateral ptosis\n- Abnormality of the hairline\n- Dilatation of the renal pelvis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- Widow's peak\n- Thick eyebrow\n- Delayed speech and language development\n- Joint laxity\n- Unilateral ptosis\n- Abnormality of the hairline\n- Dilatation of the renal pelvis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- Widow's peak\n- Thick eyebrow\n- Delayed speech and language development\n- Joint laxity\n- Unilateral ptosis\n- Abnormality of the hairline\n- Dilatation of the renal pelvis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- Widow's peak\n- Thick eyebrow\n- Delayed speech and language development\n- Joint laxity\n- Unilateral ptosis\n- Abnormality of the hairline\n- Dilatation of the renal pelvis\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Wide nasal bridge\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Sleep disturbance\n- Short stature\n- Unilateral ptosis\n- Horizontal eyebrow\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Strabismus\n- Nystagmus\n- Seizure\n- Ventriculomegaly\n- Areflexia of lower limbs\n- Severe muscular hypotonia\n- Periventricular leukomalacia\n- Severe global developmental delay\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/02017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Gingival overgrowth\n- Microcephaly\n- Retrognathia\n- Hypertelorism\n- High forehead\n- Anteverted nares\n- Widely spaced teeth\n- Single transverse palmar crease\n- Slender finger\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Joint laxity\n- Frontal bossing\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Kyphosis\n- Butterfly vertebrae\n- Short stature\n- Dysplastic pulmonary valve\n- Cholesteatoma\n- Sleep apnea\n- Feeding difficulties\n- Camptodactyly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Reduced tendon reflexes\n- Ventriculomegaly\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/02019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Macrodontia of permanent maxillary central incisor\n- Delayed speech and language development\n- Specific learning disability\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Reduced tendon reflexes\n- Severe muscular hypotonia\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/02021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Low-set ears\n- Downslanted palpebral fissures\n- Short attention span\n- Decreased response to growth hormone stimulation test\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Achilles tendon contracture\n- Sleep disturbance\n- Hyperkinetic movements\n- Highly arched eyebrow\n- Kyphosis\n- Hip dislocation\n- Bruxism\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Bilateral single transverse palmar creases\n- Almond-shaped palpebral fissure\n- Prominent forehead\n- Hypoplastic fifth toenail\n- Bronchiolitis\n- Feeding difficulties\n- Frequent temper tantrums\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Open mouth\n- Mandibular prognathia\n- Broad forehead\n- Hearing impairment\n- Bulbous nose\n- Atypical behavior\n- Hypotonia\n- Abnormal periventricular white matter morphology\n- Delayed skeletal maturation\n- Severe global developmental delay\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/02023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Broad forehead\n- Short neck\n- Hypotonia\n- Abnormal periventricular white matter morphology\n- Delayed skeletal maturation\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/02024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Macroglossia\n- Macrocephaly\n- Coarse facial features\n- Thick eyebrow\n- Hyperthyroidism\n- Seizure\n- Reduced tendon reflexes\n- Scoliosis\n- Severe muscular hypotonia\n- Severe global developmental delay\n- Periventricular white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/02025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hearing impairment\n- Preauricular skin tag\n- Downslanted palpebral fissures\n- Delayed puberty\n- Bilateral ptosis\n- Mild short stature\n- Duplication of thumb phalanx\n- Severe global developmental delay\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/02026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Plagiocephaly\n- Highly arched eyebrow\n- Short nose\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/02027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Posteriorly rotated ears\n- Abnormal pinna morphology\n- Strabismus\n- Downslanted palpebral fissures\n- Nystagmus\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Recurrent respiratory infections\n- Lymphoma\n- High, narrow palate\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Duplication of phalanx of hallux\n- 1-2 toe syndactyly\n- Intellectual disability, severe\n- High myopia\n- Prominent forehead\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Posteriorly rotated ears\n- Abnormal pinna morphology\n- Strabismus\n- Downslanted palpebral fissures\n- Nystagmus\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Recurrent respiratory infections\n- Lymphoma\n- High, narrow palate\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Duplication of phalanx of hallux\n- 1-2 toe syndactyly\n- Intellectual disability, severe\n- High myopia\n- Prominent forehead\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Scoliosis\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/02030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/02031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Nystagmus\n- Restlessness\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Growth delay\n- Umbilical hernia\n- Recurrent respiratory infections\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Bilateral postaxial polydactyly\n- Duplication of phalanx of hallux\n- Intellectual disability, severe\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Nystagmus\n- Restlessness\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Growth delay\n- Umbilical hernia\n- Recurrent respiratory infections\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Bilateral postaxial polydactyly\n- Duplication of phalanx of hallux\n- Intellectual disability, severe\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Nystagmus\n- Restlessness\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Growth delay\n- Umbilical hernia\n- Recurrent respiratory infections\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Bilateral postaxial polydactyly\n- Duplication of phalanx of hallux\n- Intellectual disability, severe\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Ptosis\n- Scoliosis\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/02035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/02036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Large fontanelles\n- Narrow face\n- Long face\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Broad forehead\n- High forehead\n- Wide nose\n- Depressed nasal ridge\n- Short neck\n- Telecanthus\n- Prominent fingertip pads\n- Hypotonia\n- Small nail\n- Hypoplasia of the corpus callosum\n- Expressive language delay\n- Highly arched eyebrow\n- Kyphoscoliosis\n- Depressed nasal bridge\n- Asymmetry of the ears\n- Prominent forehead\n- Severe global developmental delay\n- Postaxial polydactyly\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Large fontanelles\n- Narrow face\n- Long face\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Broad forehead\n- High forehead\n- Wide nose\n- Depressed nasal ridge\n- Short neck\n- Telecanthus\n- Prominent fingertip pads\n- Hypotonia\n- Small nail\n- Hypoplasia of the corpus callosum\n- Expressive language delay\n- Highly arched eyebrow\n- Kyphoscoliosis\n- Depressed nasal bridge\n- Asymmetry of the ears\n- Prominent forehead\n- Severe global developmental delay\n- Postaxial polydactyly\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/02039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Ophthalmoplegia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/02040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Myopia\n- Upslanted palpebral fissure\n- Hypotonia\n- Intellectual disability, mild\n- Diastasis recti\n- Hypoplasia of the corpus callosum\n- Enlarged cisterna magna\n- Hip dislocation\n- Thoracic kyphosis\n- Depressed nasal bridge\n- Bilateral postaxial polydactyly\n- Prominent forehead\n- Severe global developmental delay\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Myopia\n- Upslanted palpebral fissure\n- Hypotonia\n- Intellectual disability, mild\n- Diastasis recti\n- Hypoplasia of the corpus callosum\n- Enlarged cisterna magna\n- Hip dislocation\n- Thoracic kyphosis\n- Depressed nasal bridge\n- Bilateral postaxial polydactyly\n- Prominent forehead\n- Severe global developmental delay\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Scoliosis\n- Short nose\n- Depressed nasal bridge\n- Microtia\n- Short thumb\n- Broad hallux\n- Short hallux\n- Intracranial cystic lesion\n- Intellectual disability, severe\n- Prominent forehead\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/02043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Hypotonia\n- Global developmental delay\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Depressed nasal bridge\n- Pes valgus\n- Abnormal distal phalanx morphology of finger\n- Stridor\n- Tented upper lip vermilion\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Hypotonia\n- Global developmental delay\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Depressed nasal bridge\n- Pes valgus\n- Abnormal distal phalanx morphology of finger\n- Stridor\n- Tented upper lip vermilion\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Macrocephaly\n- Delayed cranial suture closure\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Tapered finger\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Joint hypermobility\n- Molar tooth sign on MRI\n- Depressed nasal bridge\n- Short finger\n- Duplication of phalanx of hallux\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Macrocephaly\n- Delayed cranial suture closure\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Tapered finger\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Joint hypermobility\n- Molar tooth sign on MRI\n- Depressed nasal bridge\n- Short finger\n- Duplication of phalanx of hallux\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Macrocephaly\n- Delayed cranial suture closure\n- Broad forehead\n- Wide nasal bridge\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Tapered finger\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Joint hypermobility\n- Molar tooth sign on MRI\n- Depressed nasal bridge\n- Short finger\n- Duplication of phalanx of hallux\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Calcaneovalgus deformity\n- Expressive language delay\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Cutaneous finger syndactyly\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Cupped ear\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Nevus flammeus\n- Hypotonia\n- Atrial septal defect\n- Patent ductus arteriosus\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Increased body weight\n- Accelerated skeletal maturation\n- Deep palmar crease\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Calcaneovalgus deformity\n- Expressive language delay\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Cutaneous finger syndactyly\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Cupped ear\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Nevus flammeus\n- Hypotonia\n- Atrial septal defect\n- Patent ductus arteriosus\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Increased body weight\n- Accelerated skeletal maturation\n- Deep palmar crease\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Broad nasal tip\n- Proptosis\n- Long eyelashes\n- Synophrys\n- Nevus flammeus\n- Hypotonia\n- Atrial septal defect\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Kyphosis\n- Deep palmar crease\n- Moderate global developmental delay\n- Feeding difficulties\n- Abnormal cardiac ventricular function\n- Choroid plexus papilloma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Broad nasal tip\n- Proptosis\n- Long eyelashes\n- Synophrys\n- Nevus flammeus\n- Hypotonia\n- Atrial septal defect\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Kyphosis\n- Deep palmar crease\n- Moderate global developmental delay\n- Feeding difficulties\n- Abnormal cardiac ventricular function\n- Choroid plexus papilloma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Intellectual disability\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Calcaneovalgus deformity\n- Expressive language delay\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- 2-5 finger cutaneous syndactyly\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Nystagmus\n- Oculomotor apraxia\n- Intellectual disability\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Calcaneovalgus deformity\n- Expressive language delay\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- 2-5 finger cutaneous syndactyly\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Macrocephaly\n- Long face\n- Hypertelorism\n- Posteriorly rotated ears\n- Proptosis\n- Hypotonia\n- Overlapping toe\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Recurrent fractures\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Macrocephaly\n- Long face\n- Hypertelorism\n- Posteriorly rotated ears\n- Proptosis\n- Hypotonia\n- Overlapping toe\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Recurrent fractures\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Macrocephaly\n- Long face\n- Hypertelorism\n- Posteriorly rotated ears\n- Proptosis\n- Hypotonia\n- Overlapping toe\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Recurrent fractures\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Unilateral renal agenesis\n- Thin upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Proptosis\n- Long eyelashes\n- Prominent fingertip pads\n- Hypotonia\n- Intrauterine growth retardation\n- Ventriculomegaly\n- Highly arched eyebrow\n- Intellectual disability, borderline\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Unilateral renal agenesis\n- Thin upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Proptosis\n- Long eyelashes\n- Prominent fingertip pads\n- Hypotonia\n- Intrauterine growth retardation\n- Ventriculomegaly\n- Highly arched eyebrow\n- Intellectual disability, borderline\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Malar flattening\n- Hypertelorism\n- Short philtrum\n- Broad nasal tip\n- Ptosis\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Short distal phalanx of toe\n- Deep plantar creases\n- Neonatal hypoglycemia\n- Intellectual disability, moderate\n- Thickened calvaria\n- High, narrow palate\n- Relative macrocephaly\n- Cervical C2\/C3 vertebral fusion\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Deep palmar crease\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n- Large earlobe\n- Short distal phalanx of finger\n- Short metacarpal\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Malar flattening\n- Hypertelorism\n- Short philtrum\n- Broad nasal tip\n- Ptosis\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Short distal phalanx of toe\n- Deep plantar creases\n- Neonatal hypoglycemia\n- Intellectual disability, moderate\n- Thickened calvaria\n- High, narrow palate\n- Relative macrocephaly\n- Cervical C2\/C3 vertebral fusion\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Deep palmar crease\n- Nevus flammeus of the forehead\n- Feeding difficulties in infancy\n- Large earlobe\n- Short distal phalanx of finger\n- Short metacarpal\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/02063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Delayed speech and language development\n- Global developmental delay\n- Small nail\n- Short distal phalanx of the thumb\n- Tented upper lip vermilion\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Long palpebral fissure\n- Pectus excavatum\n- Global developmental delay\n- Absent speech\n- Small nail\n- Short 5th metacarpal\n- Tented upper lip vermilion\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Recurrent otitis media\n- Bulbous nose\n- Anteverted nares\n- Torticollis\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Constipation\n- Gastroesophageal reflux\n- Spastic gait\n- Ventriculomegaly\n- Coarse hair\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Short nasal bridge\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Marcus Gunn jaw winking synkinesis\n- Thick hair\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Anteverted nares\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Pectus excavatum\n- Hypotonia\n- Global developmental delay\n- Broad-based gait\n- Mild short stature\n- Prominent nasolabial fold\n- Prominent nasal tip\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Abnormality of upper lip vermillion\n- Pineal cyst\n- Arachnoid cyst\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Full cheeks\n- Short philtrum\n- Anteverted nares\n- Upslanted palpebral fissure\n- Amblyopia\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Sacral dimple\n- Hypotonia\n- Failure to thrive\n- Gastroesophageal reflux\n- Broad-based gait\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Mild global developmental delay\n- Hepatitis\n- Pineal cyst\n- Elevated circulating alanine aminotransferase concentration\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Full cheeks\n- Short philtrum\n- Widely spaced teeth\n- Anxiety\n- Delayed speech and language development\n- Eczema\n- Global developmental delay\n- Brisk reflexes\n- Pes cavus\n- Achilles tendon contracture\n- Poor suck\n- Asthma\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Short nasal bridge\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Sparse lateral eyebrow\n- Feeding difficulties\n- Stereotypical hand wringing\n- Thick vermilion border\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Cleft soft palate\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Posteriorly rotated ears\n- Recurrent otitis media\n- Anteverted nares\n- Upslanted palpebral fissure\n- Intellectual disability\n- Global developmental delay\n- Brisk reflexes\n- Failure to thrive\n- Constipation\n- Bilateral tonic-clonic seizure\n- Recurrent aspiration pneumonia\n- Ventriculomegaly\n- Broad-based gait\n- Limb hypertonia\n- Inverted nipples\n- Prominent nasal tip\n- Sparse lateral eyebrow\n- Limited hip movement\n- Feeding difficulties in infancy\n- Limitation of knee mobility\n- Thick vermilion border\n- Arachnoid cyst\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Anteverted nares\n- Upslanted palpebral fissure\n- Diastema\n- Delayed speech and language development\n- Seizure\n- Motor delay\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/02073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Underdeveloped nasal alae\n- Delayed speech and language development\n- Motor delay\n- Pes planus\n- Clinodactyly of the 5th finger\n- Broad hallux\n- Short hallux\n- Intellectual disability, severe\n- Monocular strabismus\n- Severe global developmental delay\n- Long nasal bridge\n- Fibular deviation of the 2nd toe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/02074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Prominent nose\n- Autistic behavior\n- Delayed speech and language development\n- Slender finger\n- Intellectual disability, moderate\n- Low hanging columella\n- Slender toe\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/02075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Broad nasal tip\n- Myopia\n- Tooth malposition\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Small for gestational age\n- Overlapping toe\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Excessive wrinkling of palmar skin\n- Small sella turcica\n- Intellectual disability, severe\n- Severe global developmental delay\n- Short palpebral fissure\n- Esodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/02076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Microcephaly\n- Micrognathia\n- Protruding ear\n- Underdeveloped nasal alae\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Small for gestational age\n- Long nose\n- Short stature\n- Decreased body weight\n- Premature eruption of permanent teeth\n- Hypointensity of cerebral white matter on MRI\n- Broad hallux\n- Mild global developmental delay\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/02077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Micrognathia\n- Cataract\n- Hypermetropia\n- Aggressive behavior\n- Short attention span\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Sandal gap\n- Intellectual disability, moderate\n- Sleep disturbance\n- Abnormal periventricular white matter morphology\n- Decreased body weight\n- Moderate global developmental delay\n- Long nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/02078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Telecanthus\n- Myopia\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Hip dysplasia\n- Short palm\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/02079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Retinopathy\n- Oculomotor apraxia\n- Intellectual disability, mild\n- Dysarthria\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Frontal bossing\n- Gait ataxia\n- Polymicrogyria\n- EEG abnormality\n- Depressed nasal bridge\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Nystagmus\n- Oculomotor apraxia\n- Postaxial hand polydactyly\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Frontal bossing\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Nystagmus\n- Oculomotor apraxia\n- Seizure\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Frontal bossing\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/02082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypoplasia of the maxilla\n- Low-set ears\n- Sensorineural hearing impairment\n- Ptosis\n- Exotropia\n- Synophrys\n- Hypothyroidism\n- Interphalangeal joint contracture of finger\n- Motor delay\n- Hydrops fetalis\n- Hallux valgus\n- Thrombocytopenia\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Pleural effusion\n- Recurrent lower respiratory tract infections\n- Decreased circulating antibody level\n- Intellectual disability, severe\n- Midface retrusion\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Triangular face\n- Short chin\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Telecanthus\n- Specific learning disability\n- Macrodontia\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Deep palmar crease\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/02084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Triangular face\n- Short chin\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Telecanthus\n- Specific learning disability\n- Macrodontia\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Deep palmar crease\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/02085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Epicanthus\n- Pointed chin\n- Smooth philtrum\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Telecanthus\n- Specific learning disability\n- Intellectual disability, moderate\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Intellectual disability, severe\n- Malar rash\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/02086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Smooth philtrum\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Telecanthus\n- Delayed speech and language development\n- Nevus flammeus\n- Specific learning disability\n- Intellectual disability, moderate\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Intellectual disability, severe\n- Malar rash\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/02087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Smooth philtrum\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Strabismus\n- Telecanthus\n- Delayed speech and language development\n- Specific learning disability\n- Intellectual disability, moderate\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/02088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Short philtrum\n- Widely spaced teeth\n- Umbilical hernia\n- Pes planus\n- Dysphagia\n- Gastroesophageal reflux\n- Asthma\n- Short nose\n- Decreased body weight\n- Joint contracture of the 3rd finger\n- Flexion contracture of the 2nd finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Epicanthus\n- Widely spaced teeth\n- Tetralogy of Fallot\n- Scoliosis\n- Short nose\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Widely spaced teeth\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Neonatal hypotonia\n- Joint hypermobility\n- Short nose\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Narrow mouth\n- Brachycephaly\n- Wide anterior fontanel\n- Mandibular prognathia\n- Broad forehead\n- Downslanted palpebral fissures\n- Hypermetropia\n- Hypertrichosis\n- obsolete Decreased subcutaneous fat\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Umbilical hernia\n- Small nail\n- Coarse hair\n- Short stature\n- Coronal craniosynostosis\n- Partial abdominal muscle agenesis\n- Excessive wrinkled skin\n- Abnormality of the hairline\n- Underdeveloped supraorbital ridges\n- Dermal translucency\n- Primary microcephaly\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/02092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Hydrocephalus\n- Brachycephaly\n- Wide anterior fontanel\n- Mandibular prognathia\n- Broad forehead\n- Low-set ears\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Hypermetropia\n- Microphthalmia\n- Microdontia\n- Delayed speech and language development\n- Hypertrichosis\n- obsolete Decreased subcutaneous fat\n- Syndactyly\n- Motor delay\n- Muscle weakness\n- Failure to thrive\n- Intrauterine growth retardation\n- Umbilical hernia\n- Atrial septal defect\n- Patent ductus arteriosus\n- obsolete Aortic dilatation\n- Small nail\n- Gastroesophageal reflux\n- Prominent glabella\n- Pulmonary arterial hypertension\n- Hemiplegia\n- Short stature\n- Coronal craniosynostosis\n- Partial abdominal muscle agenesis\n- Excessive wrinkled skin\n- Abnormality of the hairline\n- Short distal phalanx of finger\n- Underdeveloped supraorbital ridges\n- Dermal translucency\n- Primary microcephaly\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/02093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Hydrocephalus\n- Brachycephaly\n- Wide anterior fontanel\n- Mandibular prognathia\n- Broad forehead\n- Low-set ears\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Hypermetropia\n- Microphthalmia\n- Microdontia\n- Delayed speech and language development\n- Hypertrichosis\n- obsolete Decreased subcutaneous fat\n- Syndactyly\n- Motor delay\n- Muscle weakness\n- Failure to thrive\n- Intrauterine growth retardation\n- Umbilical hernia\n- Atrial septal defect\n- Patent ductus arteriosus\n- obsolete Aortic dilatation\n- Small nail\n- Gastroesophageal reflux\n- Prominent glabella\n- Pulmonary arterial hypertension\n- Hemiplegia\n- Short stature\n- Coronal craniosynostosis\n- Partial abdominal muscle agenesis\n- Excessive wrinkled skin\n- Abnormality of the hairline\n- Short distal phalanx of finger\n- Underdeveloped supraorbital ridges\n- Dermal translucency\n- Primary microcephaly\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/02094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Neonatal hypotonia\n- Dysphagia\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Motor delay\n- Neonatal hypotonia\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Short nose\n- Depressed nasal bridge\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Short philtrum\n- Widely spaced teeth\n- Delayed speech and language development\n- Eczema\n- Motor delay\n- Short nose\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Large fontanelles\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Convex nasal ridge\n- obsolete Decreased subcutaneous fat\n- Prominent superficial veins\n- Craniosynostosis\n- Hepatic steatosis\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Umbilical hernia\n- Oligohydramnios\n- Bicuspid aortic valve\n- Small nail\n- Pulmonary arterial hypertension\n- Decreased skull ossification\n- Hypoplasia of the abdominal wall musculature\n- Excessive wrinkled skin\n- Prematurely aged appearance\n- Short distal phalanx of finger\n- Abnormality of the scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/02098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Large fontanelles\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Convex nasal ridge\n- obsolete Decreased subcutaneous fat\n- Prominent superficial veins\n- Craniosynostosis\n- Hepatic steatosis\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Umbilical hernia\n- Oligohydramnios\n- Bicuspid aortic valve\n- Small nail\n- Pulmonary arterial hypertension\n- Decreased skull ossification\n- Hypoplasia of the abdominal wall musculature\n- Excessive wrinkled skin\n- Prematurely aged appearance\n- Short distal phalanx of finger\n- Abnormality of the scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/02099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Widely spaced teeth\n- Neonatal hypotonia\n- Short stature\n- Decreased body weight\n- Cutaneous syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/02100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Large fontanelles\n- Triangular face\n- Low-set ears\n- Convex nasal ridge\n- obsolete Decreased subcutaneous fat\n- Prominent superficial veins\n- Cerebellar hypoplasia\n- Craniosynostosis\n- Intrauterine growth retardation\n- Small for gestational age\n- Umbilical hernia\n- Oligohydramnios\n- Small nail\n- Respiratory distress\n- Abnormal cortical gyration\n- Hypoplasia of the abdominal wall musculature\n- Periventricular heterotopia\n- Excessive wrinkled skin\n- Prematurely aged appearance\n- Short distal phalanx of finger\n- Abnormality of the scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/02101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the philtrum\n- Hypertelorism\n- Wide nasal bridge\n- Blepharophimosis\n- Abnormality of the ear\n- Atypical behavior\n- Delayed speech and language development\n- Hypotonia\n- Abnormal joint morphology\n- Intellectual disability, moderate\n- Midface retrusion\n- Feeding difficulties\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Horseshoe kidney\n- Delayed speech and language development\n- Hypothyroidism\n- Sacral dimple\n- Cutis marmorata\n- Motor delay\n- Limitation of joint mobility\n- Small for gestational age\n- Ventricular septal defect\n- Intellectual disability, moderate\n- Focal-onset seizure\n- Bilateral single transverse palmar creases\n- Postnatal growth retardation\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Horseshoe kidney\n- Delayed speech and language development\n- Hypothyroidism\n- Sacral dimple\n- Cutis marmorata\n- Motor delay\n- Limitation of joint mobility\n- Small for gestational age\n- Ventricular septal defect\n- Intellectual disability, moderate\n- Focal-onset seizure\n- Bilateral single transverse palmar creases\n- Postnatal growth retardation\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Pelvic kidney\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Small for gestational age\n- Gastroesophageal reflux\n- Asthma\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Postnatal growth retardation\n- Mild global developmental delay\n- Feeding difficulties\n- Allergy\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Pelvic kidney\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Small for gestational age\n- Gastroesophageal reflux\n- Asthma\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Postnatal growth retardation\n- Mild global developmental delay\n- Feeding difficulties\n- Allergy\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the philtrum\n- Hypertelorism\n- Wide nasal bridge\n- Strabismus\n- Blepharophimosis\n- Abnormality of the ear\n- Atypical behavior\n- Delayed speech and language development\n- Gynecomastia\n- Hypotonia\n- Abnormal joint morphology\n- Pes planus\n- Intellectual disability, moderate\n- Sleep disturbance\n- Midface retrusion\n- Feeding difficulties\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Delayed speech and language development\n- Eczema\n- Motor delay\n- Small for gestational age\n- Asthma\n- Intellectual disability, moderate\n- Scoliosis\n- Postnatal growth retardation\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Abnormal joint morphology\n- Pes planus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Intellectual disability, mild\n- Hiatus hernia\n- Multiple renal cysts\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Motor delay\n- Small for gestational age\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- 3-4 toe syndactyly\n- Moderate global developmental delay\n- Feeding difficulties\n- Multifocal hyperintensity of cerebral white matter on MRI\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Strabismus\n- Blepharophimosis\n- Atypical behavior\n- Gynecomastia\n- Hypotonia\n- Pes planus\n- Sleep disturbance\n- Intellectual disability, borderline\n- Midface retrusion\n- Feeding difficulties\n- Abnormality of brain morphology\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal cyst\n- Hypermetropia\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Motor delay\n- Atrial septal defect\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Radial bowing\n- Periventricular heterotopia\n- Absent thumb\n- Forearm undergrowth\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Abnormality of the philtrum\n- Wide nasal bridge\n- Atypical behavior\n- Hypotonia\n- Intellectual disability, mild\n- Abnormal joint morphology\n- Pes planus\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Keratoconus\n- Delayed speech and language development\n- Eczema\n- Tapered finger\n- Prominent fingertip pads\n- Seizure\n- Intellectual disability, mild\n- Motor delay\n- Limited elbow extension\n- Ventricular septal defect\n- Asthma\n- Scoliosis\n- 2-3 toe syndactyly\n- Attention deficit hyperactivity disorder\n- Posterior subcapsular cataract\n- Short thumb\n- Mild global developmental delay\n- Hair-pulling\n- Camptodactyly\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Pierre-Robin sequence\n- Astigmatism\n- Autistic behavior\n- Delayed speech and language development\n- Single transverse palmar crease\n- Brachydactyly\n- Prominent fingertip pads\n- Hypotonia\n- Motor delay\n- Camptodactyly of toe\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Dislocated radial head\n- Narrow nail\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Abnormality of the philtrum\n- Hypertelorism\n- Wide nasal bridge\n- Strabismus\n- Atypical behavior\n- Midface retrusion\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Small for gestational age\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Wide nasal bridge\n- Blepharophimosis\n- Atypical behavior\n- Delayed speech and language development\n- Hypotonia\n- Pes planus\n- Intellectual disability, moderate\n- Sleep disturbance\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hearing impairment\n- Tapered finger\n- Prominent fingertip pads\n- Intellectual disability, moderate\n- Scoliosis\n- Total anomalous pulmonary venous return\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Horseshoe kidney\n- Hydronephrosis\n- Hearing impairment\n- Strabismus\n- Delayed speech and language development\n- Motor delay\n- Ventricular septal defect\n- Intellectual disability, moderate\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Mixed hearing impairment\n- Autistic behavior\n- Delayed speech and language development\n- Congenital diaphragmatic hernia\n- Renal cortical cysts\n- Eczema\n- Brachydactyly\n- Prominent fingertip pads\n- Hypotonia\n- Motor delay\n- Gastroesophageal reflux\n- Gray matter heterotopia\n- Intellectual disability, moderate\n- Scoliosis\n- Postnatal growth retardation\n- Moderate global developmental delay\n- Feeding difficulties\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Abnormality of the philtrum\n- Wide nasal bridge\n- Atypical behavior\n- Delayed speech and language development\n- Global developmental delay\n- Pes planus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/02123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hyperactivity\n- Pectus excavatum\n- Hypertrichosis\n- Tapered finger\n- Motor delay\n- Dystonia\n- Short foot\n- Overlapping toe\n- Esophageal atresia\n- Intellectual disability, moderate\n- Tracheoesophageal fistula\n- Feeding difficulties in infancy\n- Postnatal growth retardation\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Intellectual disability, mild\n- Parietal foramina\n- Increased number of skin folds\n- Feeding difficulties in infancy\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal dysplasia\n- Wide mouth\n- Cleft palate\n- Thin upper lip vermilion\n- Broad forehead\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Broad nasal tip\n- Strabismus\n- Hypermetropia\n- Optic atrophy\n- Widely spaced teeth\n- Numerous nevi\n- Syndactyly\n- Intellectual disability\n- Global developmental delay\n- Bilateral ptosis\n- Small for gestational age\n- Pericardial effusion\n- Scoliosis\n- Recurrent infections\n- Immunodeficiency\n- Thick corpus callosum\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Increased corneal thickness\n- Increased mean platelet volume\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Thickened helices\n- Wide nasal bridge\n- Flared nostrils\n- Broad nasal tip\n- Webbed neck\n- Strabismus\n- Abnormal sternum morphology\n- Intellectual disability\n- Global developmental delay\n- Flexion contracture\n- Hypertrophic cardiomyopathy\n- Thrombocytopenia\n- Ventriculomegaly\n- Recurrent infections\n- Sparse hair\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Prominent forehead\n- Midface retrusion\n- Sparse eyebrow\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Thickened helices\n- Wide nasal bridge\n- Flared nostrils\n- Broad nasal tip\n- Webbed neck\n- Strabismus\n- Abnormal sternum morphology\n- Intellectual disability\n- Global developmental delay\n- Flexion contracture\n- Hypertrophic cardiomyopathy\n- Thrombocytopenia\n- Ventriculomegaly\n- Recurrent infections\n- Sparse hair\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Prominent forehead\n- Midface retrusion\n- Sparse eyebrow\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hydrocephalus\n- Broad forehead\n- Long philtrum\n- Low-set ears\n- Wide nasal bridge\n- Strabismus\n- Widely spaced teeth\n- Hypothyroidism\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Coarctation of aorta\n- Scoliosis\n- Recurrent infections\n- Total anomalous pulmonary venous return\n- Abnormal hair whorl\n- Prominent forehead\n- Broad jaw\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hydrocephalus\n- Broad forehead\n- Long philtrum\n- Low-set ears\n- Wide nasal bridge\n- Strabismus\n- Widely spaced teeth\n- Hypothyroidism\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Coarctation of aorta\n- Scoliosis\n- Recurrent infections\n- Total anomalous pulmonary venous return\n- Abnormal hair whorl\n- Prominent forehead\n- Broad jaw\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Hypertelorism\n- Wide nasal bridge\n- Flared nostrils\n- Strabismus\n- Widely spaced teeth\n- Syndactyly\n- Intellectual disability\n- Global developmental delay\n- Flexion contracture\n- Bilateral ptosis\n- Pericardial effusion\n- Ventriculomegaly\n- Abnormal cerebellar vermis morphology\n- Recurrent infections\n- Sparse hair\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Prominent forehead\n- Increased mean platelet volume\n- Camptodactyly\n- Broad jaw\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Hypertelorism\n- Wide nasal bridge\n- Flared nostrils\n- Strabismus\n- Widely spaced teeth\n- Syndactyly\n- Intellectual disability\n- Global developmental delay\n- Flexion contracture\n- Bilateral ptosis\n- Pericardial effusion\n- Ventriculomegaly\n- Abnormal cerebellar vermis morphology\n- Recurrent infections\n- Sparse hair\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Prominent forehead\n- Increased mean platelet volume\n- Camptodactyly\n- Broad jaw\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Wide mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Hypertelorism\n- Downslanted palpebral fissures\n- Myopia\n- Thick eyebrow\n- Synophrys\n- Widely spaced teeth\n- Delayed speech and language development\n- Slender finger\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Metatarsus adductus\n- Neutropenia\n- Enlarged cisterna magna\n- Downturned corners of mouth\n- Hyperactive deep tendon reflexes\n- Focal-onset seizure\n- Incisor macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/02133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Downslanted palpebral fissures\n- Long palpebral fissure\n- Widely spaced teeth\n- Diastema\n- Delayed speech and language development\n- Large for gestational age\n- Intellectual disability, moderate\n- Downturned corners of mouth\n- 2-3 toe syndactyly\n- Incisor macrodontia\n- Tented philtrum\n- Neonatal seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/02134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypospadias\n- Wide mouth\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Strabismus\n- Long palpebral fissure\n- Syndactyly\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Partial agenesis of the corpus callosum\n- Flexion contracture\n- Bilateral ptosis\n- Small for gestational age\n- Patent foramen ovale\n- Abnormal brainstem morphology\n- Enlarged posterior fossa\n- Cerebellar dysplasia\n- Sparse hair\n- Postnatal growth retardation\n- Prominent forehead\n- Midface retrusion\n- Abnormal cerebellar peduncle morphology\n- Oculomotor nerve palsy\n- Camptodactyly\n- Abnormal hippocampus morphology\n- Hyperintensity of cerebral white matter on MRI\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypospadias\n- Wide mouth\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Strabismus\n- Long palpebral fissure\n- Syndactyly\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Partial agenesis of the corpus callosum\n- Flexion contracture\n- Bilateral ptosis\n- Small for gestational age\n- Patent foramen ovale\n- Abnormal brainstem morphology\n- Enlarged posterior fossa\n- Cerebellar dysplasia\n- Sparse hair\n- Postnatal growth retardation\n- Prominent forehead\n- Midface retrusion\n- Abnormal cerebellar peduncle morphology\n- Oculomotor nerve palsy\n- Camptodactyly\n- Abnormal hippocampus morphology\n- Hyperintensity of cerebral white matter on MRI\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Wide nasal bridge\n- Strabismus\n- Visual impairment\n- Upslanted palpebral fissure\n- Nystagmus\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Anemia\n- Bilateral tonic-clonic seizure\n- Enlarged cisterna magna\n- Muscle stiffness\n- Clinodactyly of the 5th finger\n- Inferior cerebellar vermis hypoplasia\n- Primary microcephaly\n- Short palpebral fissure\n- Clonic seizure\n- Neonatal seizure\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/02137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Hearing impairment\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Cafe-au-lait spot\n- Global developmental delay\n- Anemia\n- Recurrent respiratory infections\n- Downturned corners of mouth\n- Short nasal bridge\n- Depressed nasal bridge\n- Retrocerebellar cyst\n- Inferior cerebellar vermis hypoplasia\n- Focal-onset seizure\n- Uplifted earlobe\n- Feeding difficulties\n- Upper limb hypertonia\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/02138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Thin upper lip vermilion\n- Brachycephaly\n- Smooth philtrum\n- Long philtrum\n- Recurrent otitis media\n- Bulbous nose\n- Hyperopic astigmatism\n- Long palpebral fissure\n- Nystagmus\n- Widely spaced teeth\n- Atypical behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Precocious puberty\n- Tapered finger\n- Global developmental delay\n- Broad finger\n- Pyloric stenosis\n- Bilateral tonic-clonic seizure\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Inferior cerebellar vermis hypoplasia\n- Thick corpus callosum\n- Focal-onset seizure\n- Short finger\n- Feeding difficulties\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/02139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Unilateral renal agenesis\n- Wide mouth\n- Low-set ears\n- Recurrent otitis media\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Broad nasal tip\n- Myopia\n- Long palpebral fissure\n- Synophrys\n- Hypotonia\n- Global developmental delay\n- Scoliosis\n- Downturned corners of mouth\n- Recurrent infections\n- Prominent metopic ridge\n- Attention deficit hyperactivity disorder\n- Multiple cafe-au-lait spots\n- Postnatal growth retardation\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Unilateral renal agenesis\n- Wide mouth\n- Low-set ears\n- Recurrent otitis media\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Broad nasal tip\n- Myopia\n- Long palpebral fissure\n- Synophrys\n- Hypotonia\n- Global developmental delay\n- Scoliosis\n- Downturned corners of mouth\n- Recurrent infections\n- Prominent metopic ridge\n- Attention deficit hyperactivity disorder\n- Multiple cafe-au-lait spots\n- Postnatal growth retardation\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Unilateral renal agenesis\n- Wide mouth\n- Low-set ears\n- Recurrent otitis media\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Broad nasal tip\n- Myopia\n- Long palpebral fissure\n- Synophrys\n- Hypotonia\n- Global developmental delay\n- Scoliosis\n- Downturned corners of mouth\n- Recurrent infections\n- Prominent metopic ridge\n- Attention deficit hyperactivity disorder\n- Multiple cafe-au-lait spots\n- Postnatal growth retardation\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Microcephaly\n- Epicanthus\n- Short philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Long neck\n- Long palpebral fissure\n- Optic atrophy\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Scoliosis\n- Downturned corners of mouth\n- Unilateral ptosis\n- Postnatal growth retardation\n- Low hanging columella\n- Cerebellar agenesis\n- Clinodactyly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Macrotia\n- Wide nasal bridge\n- Flared nostrils\n- Broad nasal tip\n- Webbed neck\n- Strabismus\n- Myopia\n- Long palpebral fissure\n- Abnormal sternum morphology\n- Numerous nevi\n- Bilateral ptosis\n- Deep philtrum\n- Eversion of lateral third of lower eyelids\n- Sparse hair\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Low-set ears\n- Wide nasal bridge\n- Flared nostrils\n- Broad nasal tip\n- Webbed neck\n- Strabismus\n- Optic atrophy\n- Bilateral ptosis\n- Small for gestational age\n- Pulmonic stenosis\n- Downturned corners of mouth\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/02146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/02147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/02148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/02149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/02150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Anophthalmia\n- Autistic behavior\n- Intellectual disability, moderate\n- Skeletal dysplasia\n- Short stature\n- Contractures of the large joints\n- Rhizomelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/02151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Long philtrum\n- Retinal coloboma\n- Strabismus\n- Visual impairment\n- Long eyelashes\n- Periorbital fullness\n- Deep philtrum\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/02152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Long philtrum\n- Retinal coloboma\n- Strabismus\n- Visual impairment\n- Long eyelashes\n- Microphthalmia\n- Exotropia\n- Periorbital fullness\n- Deep philtrum\n- Short long bone\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/02153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcornea\n- Microphthalmia\n- Coloboma\n- 2-3 toe syndactyly\n- Recurrent patellar dislocation\n- 3-4 finger syndactyly\n- Bilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/02154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Optic disc pallor\n- Optic nerve hypoplasia\n- Global developmental delay\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/02155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Optic disc pallor\n- Intellectual disability, mild\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/02156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Optic disc pallor\n- Compulsive behaviors\n- Autistic behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/02157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Microcephaly\n- Micrognathia\n- Narrow nasal ridge\n- Intellectual disability\n- Ataxia\n- Global developmental delay\n- Cerebellar atrophy\n- Cerebral atrophy\n- Vertigo\n- Decreased body weight\n- Low hanging columella\n- Incisor macrodontia\n- Focal tonic seizure\n- Fatigue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/02158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Recurrent otitis media\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Brachydactyly\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Hypoplastic toenails\n- Sparse scalp hair\n- Decreased body weight\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Delayed speech and language development\n- Motor delay\n- Cerebellar atrophy\n- Abnormal heart morphology\n- Hypoplastic toenails\n- Constipation\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Delayed speech and language development\n- Motor delay\n- Cerebellar atrophy\n- Abnormal heart morphology\n- Hypoplastic toenails\n- Constipation\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Everted lower lip vermilion\n- Macrocephaly\n- Narrow face\n- Long face\n- Mandibular prognathia\n- High forehead\n- Strabismus\n- Downslanted palpebral fissures\n- Hypermetropia\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Delayed speech and language development\n- Brachydactyly\n- Motor delay\n- Abnormal heart morphology\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Sparse scalp hair\n- Mild short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Intellectual disability, borderline\n- Mild global developmental delay\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Delayed speech and language development\n- Brachydactyly\n- Motor delay\n- Abnormal heart morphology\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Sparse scalp hair\n- Mild short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Intellectual disability, borderline\n- Mild global developmental delay\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Narrow face\n- Long face\n- High forehead\n- Astigmatism\n- Hypermetropia\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Brachydactyly\n- Global developmental delay\n- Hypoplastic toenails\n- Constipation\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Hypoplastic fifth toenail\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Everted lower lip vermilion\n- Macrocephaly\n- Narrow face\n- Long face\n- High forehead\n- Strabismus\n- Downslanted palpebral fissures\n- Nystagmus\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Ventriculomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- High forehead\n- Hearing impairment\n- Proptosis\n- Blue sclerae\n- Ventriculomegaly\n- Abnormal respiratory system physiology\n- Short nose\n- Abnormal bone ossification\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Recurrent otitis media\n- Delayed speech and language development\n- Brachydactyly\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Hypoplastic toenails\n- Constipation\n- Sparse scalp hair\n- Mild short stature\n- Clinodactyly of the 5th finger\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Sensorineural hearing impairment\n- Ptosis\n- Exotropia\n- Upslanted palpebral fissure\n- Dental malocclusion\n- Lymphedema\n- Global developmental delay\n- Ventriculomegaly\n- Abnormal intestine morphology\n- Highly arched eyebrow\n- Ectropion of lower eyelids\n- Midface retrusion\n- Increased mean platelet volume\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Retrognathia\n- High forehead\n- Abnormality of the outer ear\n- Proptosis\n- Blue sclerae\n- Hypertrichosis\n- Short nose\n- Severe global developmental delay\n- Midface retrusion\n- Abnormal bone ossification\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Gingival overgrowth\n- Everted lower lip vermilion\n- Retrognathia\n- High forehead\n- Hearing impairment\n- Glaucoma\n- Proptosis\n- Blue sclerae\n- Hypertrichosis\n- Hypoplasia of the corpus callosum\n- Abnormality of the respiratory system\n- Short nose\n- Everted upper lip vermilion\n- Moderate global developmental delay\n- Midface retrusion\n- Abnormal bone ossification\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Retrognathia\n- High forehead\n- Proptosis\n- Blue sclerae\n- Global developmental delay\n- Abnormality of the respiratory system\n- Scoliosis\n- Kyphosis\n- Everted upper lip vermilion\n- Moderate global developmental delay\n- Severe global developmental delay\n- Midface retrusion\n- Long fingers\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- High forehead\n- Proptosis\n- Delayed speech and language development\n- Hypertrichosis\n- Ventricular septal defect\n- Kyphosis\n- Moderate global developmental delay\n- Abnormal bone ossification\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin upper lip vermilion\n- Short philtrum\n- Ptosis\n- Exotropia\n- Dental malocclusion\n- Eczema\n- Lymphedema\n- Global developmental delay\n- Flexion contracture\n- Patent ductus arteriosus\n- Thrombocytopenia\n- Intention tremor\n- Eversion of lateral third of lower eyelids\n- Midface retrusion\n- Increased mean platelet volume\n- Impaired tandem gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/02175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Everted lower lip vermilion\n- Retrognathia\n- High forehead\n- Hearing impairment\n- Choanal stenosis\n- Proptosis\n- Blue sclerae\n- Delayed speech and language development\n- Hypertrichosis\n- Umbilical hernia\n- Pyloric stenosis\n- Abnormality of the respiratory system\n- Scoliosis\n- Kyphosis\n- Short nose\n- Everted upper lip vermilion\n- Moderate global developmental delay\n- Midface retrusion\n- Abnormal bone ossification\n- Bone fracture\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Retrognathia\n- High forehead\n- Proptosis\n- Blue sclerae\n- Ventricular septal defect\n- Scoliosis\n- Nephroblastoma\n- Kyphosis\n- Short nose\n- Everted upper lip vermilion\n- Severe global developmental delay\n- Midface retrusion\n- Abnormal bone ossification\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- High forehead\n- Proptosis\n- Blue sclerae\n- Hypertrichosis\n- Abnormality of the respiratory system\n- Scoliosis\n- Kyphosis\n- Short nose\n- Everted upper lip vermilion\n- Severe global developmental delay\n- Midface retrusion\n- Abnormal bone ossification\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Facial hypotonia\n- Telecanthus\n- Delayed speech and language development\n- Precocious puberty\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Reduced tendon reflexes\n- Neonatal hypotonia\n- Apnea\n- Poor coordination\n- Generalized muscle weakness\n- Feeding difficulties in infancy\n- Prominent forehead\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Facial hypotonia\n- Telecanthus\n- Delayed speech and language development\n- Precocious puberty\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Reduced tendon reflexes\n- Neonatal hypotonia\n- Apnea\n- Poor coordination\n- Generalized muscle weakness\n- Feeding difficulties in infancy\n- Prominent forehead\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Facial hypotonia\n- Facial asymmetry\n- High forehead\n- Upslanted palpebral fissure\n- Macrodontia of permanent maxillary central incisor\n- Anxiety\n- Delayed speech and language development\n- Broad-based gait\n- Poor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Facial hypotonia\n- Facial asymmetry\n- High forehead\n- Upslanted palpebral fissure\n- Macrodontia of permanent maxillary central incisor\n- Anxiety\n- Delayed speech and language development\n- Broad-based gait\n- Poor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Full cheeks\n- High forehead\n- Telecanthus\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Neonatal hypotonia\n- Broad-based gait\n- Poor coordination\n- Generalized muscle weakness\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Full cheeks\n- High forehead\n- Telecanthus\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Neonatal hypotonia\n- Broad-based gait\n- Poor coordination\n- Generalized muscle weakness\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Facial hypotonia\n- Anxiety\n- Seizure\n- Global developmental delay\n- Generalized hypotonia\n- Reduced tendon reflexes\n- Neonatal hypotonia\n- Dystonia\n- Absent speech\n- Frontal bossing\n- Hypothermia\n- Poor coordination\n- Inability to walk\n- Central apnea\n- Generalized muscle weakness\n- Abnormality of primary teeth\n- Feeding difficulties in infancy\n- Epileptic spasm\n- Low levels of vitamin D\n- Dyskinesia\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/02185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Hypertelorism\n- Micrognathia\n- Posteriorly rotated ears\n- Anteverted nares\n- Astigmatism\n- Myopia\n- Natal tooth\n- Prominent scalp veins\n- Intrauterine growth retardation\n- Small for gestational age\n- Overlapping toe\n- Skull asymmetry\n- Patellar dislocation\n- Flared metaphysis\n- Short nose\n- Reduced subcutaneous adipose tissue\n- Relative macrocephaly\n- Multiple prenatal fractures\n- Abnormal subcutaneous fat tissue distribution\n- Microtia\n- Long toe\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Hypertelorism\n- Micrognathia\n- Posteriorly rotated ears\n- Anteverted nares\n- Astigmatism\n- Myopia\n- Natal tooth\n- Prominent scalp veins\n- Intrauterine growth retardation\n- Small for gestational age\n- Overlapping toe\n- Skull asymmetry\n- Patellar dislocation\n- Flared metaphysis\n- Short nose\n- Reduced subcutaneous adipose tissue\n- Relative macrocephaly\n- Multiple prenatal fractures\n- Abnormal subcutaneous fat tissue distribution\n- Microtia\n- Long toe\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Broad forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Failure to thrive\n- Intrauterine growth retardation\n- Reduced subcutaneous adipose tissue\n- Sparse hair\n- Hooded eyelid\n- Sparse eyebrow\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Broad forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Failure to thrive\n- Intrauterine growth retardation\n- Reduced subcutaneous adipose tissue\n- Sparse hair\n- Hooded eyelid\n- Sparse eyebrow\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Strabismus\n- Abnormality of vision\n- Generalized hypotonia\n- Failure to thrive\n- Feeding difficulties\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Pointed chin\n- Triangular face\n- Narrow forehead\n- Low-set ears\n- Thick eyebrow\n- Natal tooth\n- Abnormal skull morphology\n- Prominent superficial veins\n- Failure to thrive\n- Intrauterine growth retardation\n- Reduced subcutaneous adipose tissue\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- High palate\n- Brachycephaly\n- Hypertelorism\n- High forehead\n- Strabismus\n- Abnormality of vision\n- Hypotonia\n- Plagiocephaly\n- Decreased fetal movement\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Sleep disturbance\n- Skeletal muscle atrophy\n- Developmental stagnation\n- Feeding difficulties\n- Delayed myelination\n- Delayed ability to walk\n- Recurrent upper and lower respiratory tract infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Abnormality of vision\n- Tooth malposition\n- Aggressive behavior\n- Autistic behavior\n- Pectus excavatum\n- Generalized hypotonia\n- Gastroesophageal reflux\n- Sleep disturbance\n- Developmental stagnation\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Mandibular prognathia\n- Pointed chin\n- Narrow forehead\n- Hearing impairment\n- Recurrent otitis media\n- Depressed nasal tip\n- Convex nasal ridge\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Nystagmus\n- Natal tooth\n- Dry skin\n- Eczema\n- Prominent superficial veins\n- Intrauterine growth retardation\n- Small for gestational age\n- Difficulty walking\n- Short stature\n- Decreased body weight\n- Knee flexion contracture\n- Keloids\n- Abnormal buccal fat pad morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Mandibular prognathia\n- Pointed chin\n- Narrow forehead\n- Hearing impairment\n- Recurrent otitis media\n- Depressed nasal tip\n- Convex nasal ridge\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Nystagmus\n- Natal tooth\n- Dry skin\n- Eczema\n- Prominent superficial veins\n- Intrauterine growth retardation\n- Small for gestational age\n- Difficulty walking\n- Short stature\n- Decreased body weight\n- Knee flexion contracture\n- Keloids\n- Abnormal buccal fat pad morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- High forehead\n- Abnormality of vision\n- Visual impairment\n- Autistic behavior\n- Sleep disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin vermilion border\n- Mandibular prognathia\n- Triangular face\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Convex nasal ridge\n- Proptosis\n- Upslanted palpebral fissure\n- Natal tooth\n- Prominent superficial veins\n- Intrauterine growth retardation\n- Small for gestational age\n- Skull asymmetry\n- Reduced subcutaneous adipose tissue\n- Abnormal subcutaneous fat tissue distribution\n- Sparse hair\n- Nasogastric tube feeding\n- Abnormal buccal fat pad morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- High palate\n- Microcephaly\n- Strabismus\n- Abnormality of vision\n- Visual impairment\n- Seizure\n- Generalized hypotonia\n- Failure to thrive\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Sleep disturbance\n- Abnormal globus pallidus morphology\n- Skeletal muscle atrophy\n- Developmental stagnation\n- Feeding difficulties\n- Delayed ability to sit\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- High palate\n- Microcephaly\n- Hypertelorism\n- High forehead\n- Strabismus\n- Abnormality of vision\n- Visual impairment\n- Autistic behavior\n- Pectus excavatum\n- Generalized hypotonia\n- Sleep disturbance\n- Skeletal muscle atrophy\n- Feeding difficulties\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Aggressive behavior\n- Generalized hypotonia\n- Plagiocephaly\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Abnormal periventricular white matter morphology\n- Skeletal muscle atrophy\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Seizure\n- Generalized hypotonia\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Developmental stagnation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Tooth malposition\n- Generalized hypotonia\n- Decreased fetal movement\n- Recurrent respiratory infections\n- Feeding difficulties\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Hypertelorism\n- High forehead\n- Strabismus\n- Tooth malposition\n- Generalized hypotonia\n- Plagiocephaly\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Strabismus\n- Aggressive behavior\n- Pectus excavatum\n- Generalized hypotonia\n- Plagiocephaly\n- Failure to thrive\n- Decreased fetal movement\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Enlarged cisterna magna\n- Sleep disturbance\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Abnormality of vision\n- Visual impairment\n- Aggressive behavior\n- Autistic behavior\n- Seizure\n- Generalized hypotonia\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Sleep disturbance\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypertelorism\n- High forehead\n- Tooth malposition\n- Generalized hypotonia\n- Plagiocephaly\n- Recurrent respiratory infections\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/02206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Autistic behavior\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Vomiting\n- Migraine\n- Gait imbalance\n- Drooling\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Abnormality of the palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macrocephaly\n- Epicanthus\n- Full cheeks\n- Hypertelorism\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Failure to thrive\n- Short columella\n- Deep philtrum\n- Frontal bossing\n- Gliosis\n- Curly hair\n- Exaggerated cupid's bow\n- Decreased body weight\n- Depressed nasal bridge\n- Prolonged neonatal jaundice\n- Dysplastic corpus callosum\n- Limb undergrowth\n- High anterior hairline\n- Overlapping fingers\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Decreased fetal movement\n- Mitral regurgitation\n- Asthma\n- Drooling\n- Sleep disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Epicanthus\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Absent speech\n- Joint hypermobility\n- Intellectual disability, profound\n- Scoliosis\n- Axial hypotonia\n- Tonic seizure\n- Long fingers\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Epicanthus\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Absent speech\n- Joint hypermobility\n- Intellectual disability, profound\n- Scoliosis\n- Axial hypotonia\n- Long fingers\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Atrial septal defect\n- Highly arched eyebrow\n- Short nose\n- Decreased body weight\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Large earlobe\n- Long toe\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Alternating esotropia\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Talipes equinovarus\n- Polymicrogyria\n- Intellectual disability, moderate\n- Short stature\n- Decreased body weight\n- Relative macrocephaly\n- Dysplastic corpus callosum\n- Myoclonic seizure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Dolichocephaly\n- Epicanthus\n- Narrow forehead\n- High forehead\n- Delayed speech and language development\n- Global developmental delay\n- Generalized hypotonia\n- Hypoplasia of the corpus callosum\n- Sleep apnea\n- Delayed fine motor development\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Highly arched eyebrow\n- Short nose\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Large earlobe\n- Tetralogy of Fallot with pulmonary atresia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Brisk reflexes\n- Hypoglycemia\n- Polymicrogyria\n- Limb hypertonia\n- Tented upper lip vermilion\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/02216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Hypermetropia\n- Synophrys\n- Delayed speech and language development\n- Hyperactivity\n- Motor delay\n- Generalized hypotonia\n- Specific learning disability\n- Bilateral tonic-clonic seizure\n- Asthma\n- Highly arched eyebrow\n- Recurrent infections\n- Short nose\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ectopic kidney\n- Macrocephaly\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Synophrys\n- Delayed speech and language development\n- Pectus excavatum\n- Specific learning disability\n- Large for gestational age\n- Umbilical hernia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Secundum atrial septal defect\n- Highly arched eyebrow\n- Scoliosis\n- Bronchomalacia\n- Short nose\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Myopia\n- Nystagmus\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Ventricular septal defect\n- Patent foramen ovale\n- Neutropenia\n- Limb hypertonia\n- Highly arched eyebrow\n- Recurrent infections\n- Short nose\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Axial hypotonia\n- Large earlobe\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Shawl scrotum\n- Tall stature\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Macrotia\n- Webbed neck\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Ventricular septal defect\n- Tetralogy of Fallot\n- Secundum atrial septal defect\n- Overlapping toe\n- Long hallux\n- Highly arched eyebrow\n- Short nose\n- Increased body weight\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Triangular face\n- Prominent nose\n- Strabismus\n- Myopia\n- Synophrys\n- Delayed speech and language development\n- Numerous nevi\n- Motor delay\n- Specific learning disability\n- Omphalocele\n- Polyhydramnios\n- Patent ductus arteriosus\n- Exaggerated cupid's bow\n- Highly arched eyebrow\n- Intestinal malrotation\n- Narrow palm\n- Increased body weight\n- Generalized hypertrichosis\n- Atrioventricular canal defect\n- Abnormally folded helix\n- Large earlobe\n- Open bite\n- Parachute mitral valve\n- Thick vermilion border\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Pointed chin\n- Short philtrum\n- Triangular face\n- Prominent nose\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Muscle weakness\n- Specific learning disability\n- Large for gestational age\n- Polyhydramnios\n- Ventricular septal defect\n- Atrial septal defect\n- Double outlet right ventricle\n- Overlapping toe\n- Exaggerated cupid's bow\n- Highly arched eyebrow\n- Narrow palm\n- Increased body weight\n- Generalized hypertrichosis\n- Thoracic kyphoscoliosis\n- 2-3 toe cutaneous syndactyly\n- Focal-onset seizure\n- Progressive ptosis\n- Abnormally folded helix\n- Large earlobe\n- Thick vermilion border\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Pointed chin\n- Triangular face\n- Long philtrum\n- Low-set ears\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Ventricular septal defect\n- Atrial septal defect\n- Double outlet right ventricle\n- Dysphagia\n- Highly arched eyebrow\n- Short nose\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Large earlobe\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/02223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Full cheeks\n- Narrow forehead\n- Long philtrum\n- Broad nasal tip\n- Anteverted nares\n- Global developmental delay\n- Joint laxity\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Truncus arteriosus\n- Micromelia\n- Short stature\n- Laryngotracheomalacia\n- Prominent forehead\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/02224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Full cheeks\n- Narrow forehead\n- Long philtrum\n- Broad nasal tip\n- Anteverted nares\n- Global developmental delay\n- Joint laxity\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Truncus arteriosus\n- Micromelia\n- Short stature\n- Laryngotracheomalacia\n- Prominent forehead\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/02225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Autistic behavior\n- Pectus excavatum\n- Global developmental delay\n- Joint laxity\n- Aortic regurgitation\n- Scoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Pes valgus\n- Branchial cyst\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/02226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Autistic behavior\n- Pectus excavatum\n- Global developmental delay\n- Joint laxity\n- Aortic regurgitation\n- Scoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Pes valgus\n- Branchial cyst\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/02227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Autistic behavior\n- Pectus excavatum\n- Global developmental delay\n- Joint laxity\n- Aortic regurgitation\n- Scoliosis\n- Short middle phalanx of the 5th finger\n- Short stature\n- Pes valgus\n- Branchial cyst\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/02228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Pelvic kidney\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Long philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Short neck\n- Optic nerve hypoplasia\n- Brachydactyly\n- Global developmental delay\n- Joint laxity\n- Pes planus\n- Sandal gap\n- Hypoplasia of the corpus callosum\n- Short stature\n- Atrioventricular canal defect\n- Short hallux\n- Prominent forehead\n- Bilateral trilobed lung\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/02229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Conductive hearing impairment\n- Narrow nose\n- Hypotonia\n- Ventriculomegaly\n- Drooling\n- Delayed epiphyseal ossification\n- Kyphosis\n- Short stature\n- Hyperpigmented nevi\n- Sparse hair\n- Vertebral hypoplasia\n- Feeding difficulties\n- Flat face\n- Chronic constipation\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Short sternum\n- Failure to thrive\n- Aortic regurgitation\n- Abnormal left ventricle morphology\n- Frontal bossing\n- Early balding\n- Intellectual disability, moderate\n- Narrow palm\n- Prominent nasal tip\n- Wide intermamillary distance\n- Sparse hair\n- Long palm\n- Feeding difficulties\n- Chronic constipation\n- Short palpebral fissure\n- Morgagni diaphragmatic hernia\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Delayed speech and language development\n- Hyperactivity\n- Spastic diplegia\n- Motor delay\n- Patent ductus arteriosus\n- Constipation\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Polymicrogyria\n- Recurrent respiratory infections\n- Incoordination\n- Expressive language delay\n- Obstructive sleep apnea\n- Attention deficit hyperactivity disorder\n- Morgagni diaphragmatic hernia\n- Intraventricular hemorrhage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Bifid uvula\n- High palate\n- Large fontanelles\n- Epicanthus\n- Smooth philtrum\n- Triangular face\n- Facial hemangioma\n- Abnormal pinna morphology\n- Small earlobe\n- Stenosis of the external auditory canal\n- Recurrent otitis media\n- Broad nasal tip\n- Astigmatism\n- Long eyelashes\n- Hypermetropia\n- Upslanted palpebral fissure\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Hypertrichosis\n- Hypotonia\n- Plagiocephaly\n- Growth delay\n- Small for gestational age\n- Atrial septal defect\n- Mitral valve prolapse\n- Patent ductus arteriosus\n- Tricuspid valve prolapse\n- Incoordination\n- Nevus\n- Decreased body weight\n- Carotid artery tortuosity\n- Flat occiput\n- Sparse hair\n- Hypoplastic vertebral bodies\n- Medial flaring of the eyebrow\n- Absent crus of helix\n- Feeding difficulties\n- Flat face\n- Left-to-right shunt\n- Chronic constipation\n- Moderate conductive hearing impairment\n- Esodeviation\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- High palate\n- Mandibular prognathia\n- Hearing impairment\n- Low-set ears\n- Torticollis\n- Blepharophimosis\n- Pectus excavatum\n- Hypotonia\n- Dysarthria\n- Global developmental delay\n- Plagiocephaly\n- Failure to thrive\n- Intrauterine growth retardation\n- Polyhydramnios\n- Atrial septal defect\n- Patent ductus arteriosus\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Sleep disturbance\n- Corneal opacity\n- Sparse hair\n- Feeding difficulties in infancy\n- Abnormal helix morphology\n- Flat face\n- Anisometropia\n- Retinal vascular tortuosity\n- Hyperintensity of cerebral white matter on MRI\n- Nocturnal seizures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Torticollis\n- Exotropia\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Polyhydramnios\n- Hypoglycemia\n- Gastroesophageal reflux\n- Sleep disturbance\n- Aortic root aneurysm\n- Thoracolumbar scoliosis\n- Episodic metabolic acidosis\n- Microtia\n- Crumpled ear\n- Allergy\n- Chronic constipation\n- Dilation of Virchow-Robin spaces\n- Vertebrobasilar dolichoectasia\n- Deep cerebral white matter hyperintensities\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Triangular face\n- Abnormal pinna morphology\n- Telecanthus\n- Pectus carinatum\n- Global developmental delay\n- Neonatal hypotonia\n- Cerebellar vermis hypoplasia\n- Abnormal cortical gyration\n- Relative macrocephaly\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Hypertelorism\n- Posteriorly rotated ears\n- Recurrent otitis media\n- Pectus excavatum\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Growth delay\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Relative macrocephaly\n- Supraventricular tachycardia\n- Ascending tubular aorta aneurysm\n- Depressed nasal bridge\n- Deep cerebral white matter hyperintensities\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Low-set ears\n- Abnormal pinna morphology\n- Prominent nose\n- Astigmatism\n- Microdontia\n- Short attention span\n- Adducted thumb\n- Plagiocephaly\n- Failure to thrive\n- Intrauterine growth retardation\n- Constipation\n- Gastroesophageal reflux\n- Hypoventilation\n- Decreased body weight\n- Sparse hair\n- Increased nuchal translucency\n- Echogenic fetal bowel\n- Feeding difficulties\n- Phonic tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Brachycephaly\n- Anteverted nares\n- Anxiety\n- Hypotonia\n- Global developmental delay\n- Vomiting\n- Polymicrogyria\n- Cavum septum pellucidum\n- Short nose\n- Decreased body weight\n- Redundant neck skin\n- Microtia\n- Feeding difficulties\n- Flat face\n- Deep cerebral white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/02240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Motor delay\n- Agenesis of corpus callosum\n- Intellectual disability, borderline\n- Frequent temper tantrums\n- Sleep onset insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- High palate\n- Macrocephaly\n- Malar flattening\n- Long face\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Joint laxity\n- Decreased fetal movement\n- Sleep disturbance\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Flat face\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- High palate\n- Macrocephaly\n- Malar flattening\n- Long face\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Joint laxity\n- Decreased fetal movement\n- Sleep disturbance\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Flat face\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Macrocephaly\n- High forehead\n- Anteverted nares\n- Nasolacrimal duct obstruction\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Patent ductus arteriosus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Absent earlobe\n- Broad nasal tip\n- Deeply set eye\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Aggressive behavior\n- Anxiety\n- Delayed speech and language development\n- Single transverse palmar crease\n- Brachydactyly\n- Prominent fingertip pads\n- Attention deficit hyperactivity disorder\n- Microtia\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Macrocephaly\n- Retrognathia\n- Smooth philtrum\n- Recurrent otitis media\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Aggressive behavior\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Large for gestational age\n- Pes planus\n- Sandal gap\n- Ventriculomegaly\n- Inverted nipples\n- Increased body weight\n- Sparse lateral eyebrow\n- Recurrent pneumonia\n- Microtia\n- Long toe\n- Abnormal temper tantrums\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Macrocephaly\n- Retrognathia\n- Smooth philtrum\n- Recurrent otitis media\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Aggressive behavior\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Large for gestational age\n- Pes planus\n- Sandal gap\n- Ventriculomegaly\n- Inverted nipples\n- Increased body weight\n- Sparse lateral eyebrow\n- Recurrent pneumonia\n- Microtia\n- Long toe\n- Abnormal temper tantrums\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Narrow mouth\n- Everted lower lip vermilion\n- Epicanthus\n- Low-set ears\n- Narrow nasal bridge\n- Hypermetropia\n- Esotropia\n- Autistic behavior\n- Delayed speech and language development\n- Hypertrichosis\n- Prominent fingertip pads\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Specific learning disability\n- Bicuspid aortic valve\n- Recurrent infections\n- Short nose\n- Tricuspid regurgitation\n- Sparse lateral eyebrow\n- Attention deficit hyperactivity disorder\n- Microtia\n- Radial deviation of the 4th finger\n- Short 4th metacarpal\n- Short 5th metacarpal\n- Broad thumb\n- Feeding difficulties\n- Short palpebral fissure\n- Systolic heart murmur\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Trigonocephaly\n- Epicanthus\n- Long philtrum\n- Low-set ears\n- Psychotic episodes\n- Autistic behavior\n- Impaired social interactions\n- Anxiety\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Bicuspid aortic valve\n- Abdominal distention\n- Attention deficit hyperactivity disorder\n- Microtia\n- Abdominal wall muscle weakness\n- Feeding difficulties\n- Unilateral cryptorchidism\n- Short palpebral fissure\n- Auditory sensitivity\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Trigonocephaly\n- Epicanthus\n- Long philtrum\n- Low-set ears\n- Psychotic episodes\n- Autistic behavior\n- Impaired social interactions\n- Anxiety\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Bicuspid aortic valve\n- Abdominal distention\n- Attention deficit hyperactivity disorder\n- Microtia\n- Abdominal wall muscle weakness\n- Feeding difficulties\n- Unilateral cryptorchidism\n- Short palpebral fissure\n- Auditory sensitivity\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Tall stature\n- Macrocephaly\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Cerebral atrophy\n- Intellectual disability, moderate\n- Meningocele\n- Intracranial cystic lesion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/02251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Decreased fetal movement\n- Short foot\n- Gastroesophageal reflux\n- Kyphoscoliosis\n- Short stature\n- Temperature instability\n- Sleep apnea\n- Feeding difficulties\n- Chronic constipation\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Feeding difficulties\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Flexion contracture\n- Short foot\n- Short stature\n- Sleep apnea\n- Skin-picking\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Decreased fetal movement\n- Short foot\n- Gastroesophageal reflux\n- Short stature\n- Temperature instability\n- Sleep apnea\n- Feeding difficulties\n- Chronic constipation\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the eye\n- Hypotonia\n- Neonatal hypotonia\n- Flexion contracture\n- Kyphoscoliosis\n- Short stature\n- Increased body weight\n- Sleep apnea\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Decreased fetal movement\n- Short stature\n- Sleep apnea\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the eye\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Short foot\n- Gastroesophageal reflux\n- Polyphagia\n- Short stature\n- Increased body weight\n- Sleep apnea\n- Feeding difficulties\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Gastroesophageal reflux\n- Short stature\n- Temperature instability\n- Feeding difficulties\n- Skin-picking\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the eye\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Decreased fetal movement\n- Short foot\n- Kyphoscoliosis\n- Feeding difficulties\n- Skin-picking\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Wide mouth\n- Coarse facial features\n- Autistic behavior\n- Tapered finger\n- Intellectual disability\n- Lethargy\n- Global developmental delay\n- Neonatal hypotonia\n- Brisk reflexes\n- Joint hypermobility\n- Weak cry\n- Talipes equinovarus\n- Constipation\n- Poor suck\n- Scoliosis\n- Increased body weight\n- Feeding difficulties\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Wide mouth\n- Coarse facial features\n- Autistic behavior\n- Tapered finger\n- Intellectual disability\n- Lethargy\n- Global developmental delay\n- Neonatal hypotonia\n- Brisk reflexes\n- Joint hypermobility\n- Weak cry\n- Talipes equinovarus\n- Constipation\n- Poor suck\n- Scoliosis\n- Increased body weight\n- Feeding difficulties\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Hypogonadism\n- Wide mouth\n- Macroglossia\n- Prominent nasal bridge\n- Abnormality of the eye\n- Strabismus\n- Deeply set eye\n- Aggressive behavior\n- Autistic behavior\n- Decreased response to growth hormone stimulation test\n- Tapered finger\n- Hypotonia\n- Lethargy\n- Absent speech\n- Umbilical hernia\n- Weak cry\n- Fair hair\n- Congenital contracture\n- Elbow flexion contracture\n- Limb joint contracture\n- Short stature\n- Prominent nasal tip\n- Sparse hair\n- Speech articulation difficulties\n- Low hanging columella\n- Severe global developmental delay\n- Feeding difficulties\n- Skin-picking\n- Camptodactyly\n- Abnormal temper tantrums\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Hypothyroidism\n- Intellectual disability, mild\n- Motor delay\n- Neonatal hypotonia\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Scoliosis\n- Congenital contracture\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Dyslexia\n- Sleep apnea\n- Feeding difficulties\n- Reduced social reciprocity\n- Abnormal temper tantrums\n- Nasogastric tube feeding\n- Mania\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Hypothyroidism\n- Intellectual disability, mild\n- Motor delay\n- Neonatal hypotonia\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Scoliosis\n- Congenital contracture\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Dyslexia\n- Sleep apnea\n- Feeding difficulties\n- Reduced social reciprocity\n- Abnormal temper tantrums\n- Nasogastric tube feeding\n- Mania\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Hypothyroidism\n- Intellectual disability, mild\n- Motor delay\n- Neonatal hypotonia\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Scoliosis\n- Congenital contracture\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Dyslexia\n- Sleep apnea\n- Feeding difficulties\n- Reduced social reciprocity\n- Abnormal temper tantrums\n- Nasogastric tube feeding\n- Mania\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Hypothyroidism\n- Intellectual disability, mild\n- Motor delay\n- Neonatal hypotonia\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Scoliosis\n- Congenital contracture\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Dyslexia\n- Sleep apnea\n- Feeding difficulties\n- Reduced social reciprocity\n- Abnormal temper tantrums\n- Nasogastric tube feeding\n- Mania\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Motor delay\n- Neonatal hypotonia\n- Constipation\n- Poor suck\n- Scoliosis\n- Congenital contracture\n- Sleep-wake cycle disturbance\n- Feeding difficulties in infancy\n- Sleep apnea\n- Atypical repetitive behaviors\n- Nasogastric tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Motor delay\n- Neonatal hypotonia\n- Constipation\n- Poor suck\n- Scoliosis\n- Congenital contracture\n- Sleep-wake cycle disturbance\n- Feeding difficulties in infancy\n- Sleep apnea\n- Atypical repetitive behaviors\n- Nasogastric tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Motor delay\n- Neonatal hypotonia\n- Constipation\n- Poor suck\n- Scoliosis\n- Congenital contracture\n- Sleep-wake cycle disturbance\n- Feeding difficulties in infancy\n- Sleep apnea\n- Atypical repetitive behaviors\n- Nasogastric tube feeding\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Excessive daytime somnolence\n- Motor delay\n- Neonatal hypotonia\n- Specific learning disability\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Feeding difficulties in infancy\n- Reduced social reciprocity\n- Atypical repetitive behaviors\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Excessive daytime somnolence\n- Motor delay\n- Neonatal hypotonia\n- Specific learning disability\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Feeding difficulties in infancy\n- Reduced social reciprocity\n- Atypical repetitive behaviors\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Excessive daytime somnolence\n- Motor delay\n- Neonatal hypotonia\n- Specific learning disability\n- Decreased fetal movement\n- Constipation\n- Poor suck\n- Polyphagia\n- Increased body weight\n- Sleep-wake cycle disturbance\n- Feeding difficulties in infancy\n- Reduced social reciprocity\n- Atypical repetitive behaviors\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anxiety\n- Motor delay\n- Polyphagia\n- Scoliosis\n- Congenital contracture\n- Sleep-wake cycle disturbance\n- Skin-picking\n- Reduced social reciprocity\n- Atypical repetitive behaviors\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anxiety\n- Motor delay\n- Polyphagia\n- Scoliosis\n- Congenital contracture\n- Sleep-wake cycle disturbance\n- Skin-picking\n- Reduced social reciprocity\n- Atypical repetitive behaviors\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/02275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Macrotia\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Global developmental delay\n- Atrial septal defect\n- Hypoplastic fingernail\n- Anal atresia\n- Large fleshy ears\n- Expressive language delay\n- Delayed skeletal maturation\n- Elevated circulating alkaline phosphatase concentration\n- Perineal fistula\n- Shortening of all distal phalanges of the fingers\n- Large earlobe\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Aniridia\n- Microphthalmia\n- Thin skin\n- Syndactyly\n- Gastroesophageal reflux\n- Recurrent aspiration pneumonia\n- Nail dysplasia\n- Absent nipple\n- Short stature\n- Ectrodactyly\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/02277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Chorioretinal coloboma\n- Microphthalmia\n- Sparse eyelashes\n- Hypodontia\n- Dry skin\n- Short stature\n- Decreased body weight\n- Generalized abnormality of skin\n- Midface retrusion\n- Sparse eyebrow\n- Ectrodactyly\n- Toenail dysplasia\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/02278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Small earlobe\n- Protruding ear\n- Anophthalmia\n- Hypodontia\n- Syndactyly\n- Absent fingernail\n- Scoliosis\n- Decreased body weight\n- Focal dermal aplasia\/hypoplasia\n- Ectrodactyly\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/02279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Cryptorchidism\n- Macroglossia\n- Cleft palate\n- Long face\n- Short philtrum\n- Broad forehead\n- Micrognathia\n- High forehead\n- Low-set ears\n- Prominent nasal bridge\n- Nasolacrimal duct obstruction\n- Dacryocystitis\n- Microdontia\n- Diastema\n- Aggressive behavior\n- Thin skin\n- Cerebellar hypoplasia\n- Absent speech\n- Talipes equinovarus\n- Dysphagia\n- Poor suck\n- Ventriculomegaly\n- Broad-based gait\n- Curly hair\n- Fair hair\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Hypoplastic nipples\n- Flat occiput\n- Sparse hair\n- Decreased testicular size\n- Postnatal growth retardation\n- Axial hypotonia\n- Intellectual disability, severe\n- Head-banging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/02280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Abnormality of the dentition\n- High palate\n- Microcephaly\n- Facial asymmetry\n- Recurrent otitis media\n- Prominent nasal bridge\n- Wide nasal bridge\n- Retinal coloboma\n- Iris coloboma\n- Dacryocystitis\n- Atypical behavior\n- Restlessness\n- Emotional lability\n- Autistic behavior\n- Hyperactivity\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Dysphagia\n- Poor suck\n- Thoracic kyphosis\n- Prominent metopic ridge\n- Sparse hair\n- Postnatal growth retardation\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/02281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Narrow face\n- Long face\n- Micrognathia\n- Low-set ears\n- Prominent nose\n- Downslanted palpebral fissures\n- Dental crowding\n- Restlessness\n- Emotional lability\n- Hyperactivity\n- Arachnodactyly\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Fine hair\n- Abnormal patella morphology\n- Feeding difficulties\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/02282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Cleft palate\n- Narrow palate\n- Mandibular prognathia\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Cupped ear\n- Protruding ear\n- Anteverted nares\n- Downslanted palpebral fissures\n- Dental crowding\n- Pectus excavatum\n- Hypotonia\n- Joint laxity\n- Broad-based gait\n- Postural instability\n- Broad hallux\n- Broad thumb\n- Moderate global developmental delay\n- Feeding difficulties\n- Nasogastric tube feeding\n- Agenesis of maxillary incisor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/02283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Recurrent otitis media\n- Anteverted nares\n- Dental crowding\n- Aggressive behavior\n- Hypotonia\n- Short nose\n- Short stature\n- Decreased body weight\n- Prominent forehead\n- Severe global developmental delay\n- Feeding difficulties\n- Tip-toe gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/02284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Hypotonia\n- Curly hair\n- Generalized hypopigmentation\n- Mild global developmental delay\n- Feeding difficulties\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/02285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft soft palate\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Abnormality of the ear\n- Sparse eyelashes\n- Abnormal thumb morphology\n- Radioulnar synostosis\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Downslanted palpebral fissures\n- Abnormality of the ear\n- Congenital diaphragmatic hernia\n- Abnormal thumb morphology\n- Ventricular septal defect\n- Radioulnar synostosis\n- Midface retrusion\n- Abnormal radial ray morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Downslanted palpebral fissures\n- Abnormality of the ear\n- Global developmental delay\n- Abnormal foot morphology\n- Abnormal metacarpal morphology\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Downslanted palpebral fissures\n- Genu valgum\n- Radioulnar synostosis\n- Pes valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Abnormality of the ear\n- Sparse eyelashes\n- Short thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Abnormality of the ear\n- Abnormal thumb morphology\n- Absent lower eyelashes\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Hearing impairment\n- Downslanted palpebral fissures\n- Abnormality of the ear\n- Absent thumb\n- Short thumb\n- Abnormal soft palate morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/02292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Microcephaly\n- Micrognathia\n- Narrow chest\n- Missing ribs\n- Abnormality of the vertebral column\n- Failure to thrive\n- Ventricular septal defect\n- Gastroesophageal reflux\n- Scoliosis\n- Mild global developmental delay\n- Nasogastric tube feeding in infancy\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Narrow chest\n- Abnormality of the vertebral column\n- Polyhydramnios\n- Atrial septal defect\n- Short stature\n- Decreased body weight\n- Hyperechogenic kidneys\n- Mild global developmental delay\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Narrow chest\n- Abnormality of the vertebral column\n- Short stature\n- Nasogastric tube feeding in infancy\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Oligodontia\n- Delayed speech and language development\n- Narrow chest\n- Abnormality of the vertebral column\n- Decreased body weight\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Microcephaly\n- Micrognathia\n- Narrow chest\n- Small for gestational age\n- Patent ductus arteriosus\n- Gastroesophageal reflux\n- Cervical C2\/C3 vertebral fusion\n- Increased nuchal translucency\n- Nasogastric tube feeding in infancy\n- Posterior rib gap\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Narrow chest\n- Polyhydramnios\n- Nasogastric tube feeding in infancy\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Narrow chest\n- Abnormality of the vertebral column\n- Scoliosis\n- Decreased body weight\n- Increased nuchal translucency\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Chordee\n- Cleft palate\n- Microcephaly\n- Micrognathia\n- Narrow chest\n- Talipes equinovarus\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n- Nasogastric tube feeding in infancy\n- Rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/02300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Short foot\n- Short toe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Low-set ears\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low-set ears\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/02309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin vermilion border\n- Square face\n- Short philtrum\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Telecanthus\n- Long eyelashes\n- Hypermetropia\n- Autistic behavior\n- Intellectual disability, mild\n- Constipation\n- Migraine\n- Low posterior hairline\n- Recurrent upper respiratory tract infections\n- Increased body weight\n- Tooth agenesis\n- Cutaneous finger syndactyly\n- Fused teeth\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin vermilion border\n- Square face\n- Short philtrum\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Telecanthus\n- Long eyelashes\n- Hypermetropia\n- Autistic behavior\n- Intellectual disability, mild\n- Constipation\n- Migraine\n- Low posterior hairline\n- Recurrent upper respiratory tract infections\n- Increased body weight\n- Tooth agenesis\n- Cutaneous finger syndactyly\n- Fused teeth\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin vermilion border\n- Square face\n- Short philtrum\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Telecanthus\n- Long eyelashes\n- Hypermetropia\n- Autistic behavior\n- Intellectual disability, mild\n- Constipation\n- Migraine\n- Low posterior hairline\n- Recurrent upper respiratory tract infections\n- Increased body weight\n- Tooth agenesis\n- Cutaneous finger syndactyly\n- Fused teeth\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin vermilion border\n- Square face\n- Short philtrum\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Telecanthus\n- Long eyelashes\n- Hypermetropia\n- Autistic behavior\n- Intellectual disability, mild\n- Constipation\n- Migraine\n- Low posterior hairline\n- Recurrent upper respiratory tract infections\n- Increased body weight\n- Tooth agenesis\n- Cutaneous finger syndactyly\n- Fused teeth\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Thin upper lip vermilion\n- Square face\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Hypothyroidism\n- Acne\n- Seizure\n- Intellectual disability, mild\n- Pes cavus\n- Hammertoe\n- Constipation\n- Recurrent upper respiratory tract infections\n- Genu valgum\n- Swan neck-like deformities of the fingers\n- Multiple unerupted teeth\n- Cutaneous finger syndactyly\n- Feeding difficulties\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Underdeveloped nasal alae\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Autistic behavior\n- Brachydactyly\n- Limited elbow extension\n- Joint stiffness\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Constipation\n- Tethered cord\n- Dislocated radial head\n- Short stature\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Underdeveloped nasal alae\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Autistic behavior\n- Brachydactyly\n- Limited elbow extension\n- Joint stiffness\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Constipation\n- Tethered cord\n- Dislocated radial head\n- Short stature\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Underdeveloped nasal alae\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Autistic behavior\n- Brachydactyly\n- Limited elbow extension\n- Joint stiffness\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Constipation\n- Tethered cord\n- Dislocated radial head\n- Short stature\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Underdeveloped nasal alae\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Autistic behavior\n- Brachydactyly\n- Limited elbow extension\n- Joint stiffness\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Constipation\n- Tethered cord\n- Dislocated radial head\n- Short stature\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Underdeveloped nasal alae\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Autistic behavior\n- Brachydactyly\n- Limited elbow extension\n- Joint stiffness\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Constipation\n- Tethered cord\n- Dislocated radial head\n- Short stature\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Microcephaly\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Underdeveloped nasal alae\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Autistic behavior\n- Brachydactyly\n- Limited elbow extension\n- Joint stiffness\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Constipation\n- Tethered cord\n- Dislocated radial head\n- Short stature\n- Intellectual disability, severe\n- Prominent forehead\n- Feeding difficulties\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Small for gestational age\n- Umbilical hernia\n- Overlapping toe\n- Short columella\n- Short nose\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Sparse hair\n- Laryngeal cartilage malformation\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Small for gestational age\n- Umbilical hernia\n- Overlapping toe\n- Short columella\n- Short nose\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Sparse hair\n- Laryngeal cartilage malformation\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Small for gestational age\n- Umbilical hernia\n- Overlapping toe\n- Short columella\n- Short nose\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Sparse hair\n- Laryngeal cartilage malformation\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Thin upper lip vermilion\n- Long philtrum\n- Narrow nasal bridge\n- Cataract\n- Upslanted palpebral fissure\n- Autistic behavior\n- Intellectual disability, mild\n- Limited elbow extension\n- Umbilical hernia\n- Hammertoe\n- Sandal gap\n- Scoliosis\n- Kyphoscoliosis\n- Deviation of the hallux\n- Prominent inferior crus of antihelix\n- Feeding difficulties\n- Decreased circulating androgen concentration\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Everted lower lip vermilion\n- Microcephaly\n- Full cheeks\n- Microretrognathia\n- Square face\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Short columella\n- Deep philtrum\n- Highly arched eyebrow\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Sparse hair\n- Deviation of the hallux\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Flat face\n- Short palpebral fissure\n- Preaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Everted lower lip vermilion\n- Microcephaly\n- Full cheeks\n- Microretrognathia\n- Square face\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Short columella\n- Deep philtrum\n- Highly arched eyebrow\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Sparse hair\n- Deviation of the hallux\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Intellectual disability, severe\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Flat face\n- Short palpebral fissure\n- Preaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Full cheeks\n- Microretrognathia\n- Square face\n- Long philtrum\n- Low-set ears\n- Absent earlobe\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Small for gestational age\n- Overlapping toe\n- Sandal gap\n- Short columella\n- Intestinal malrotation\n- Short nose\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Sparse hair\n- Deviation of the hallux\n- Broad hallux\n- Bilateral fetal pyelectasis\n- Prominent forehead\n- Prominent inferior crus of antihelix\n- Feeding difficulties\n- Short palpebral fissure\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Hydronephrosis\n- Cleft palate\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Microretrognathia\n- Square face\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Overfolded helix\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Short neck\n- Strabismus\n- Telecanthus\n- Ptosis\n- Cataract\n- Microphthalmia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Blindness\n- Single transverse palmar crease\n- Seizure\n- Atrial septal defect\n- Patent ductus arteriosus\n- Short columella\n- Hypoplasia of the corpus callosum\n- Congenital contracture\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Depressed nasal bridge\n- Sparse hair\n- Deviation of the hallux\n- Cutaneous syndactyly of toes\n- Intellectual disability, severe\n- Prominent forehead\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Microretrognathia\n- Long philtrum\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Telecanthus\n- Ptosis\n- Hypermetropia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Agenesis of corpus callosum\n- Ventricular septal defect\n- Overlapping toe\n- Short columella\n- Deep philtrum\n- Constipation\n- Intellectual disability, moderate\n- Short nose\n- Depressed nasal bridge\n- Deviation of the hallux\n- Everted upper lip vermilion\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Short palpebral fissure\n- Colonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Microretrognathia\n- Long philtrum\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Telecanthus\n- Ptosis\n- Hypermetropia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Agenesis of corpus callosum\n- Ventricular septal defect\n- Overlapping toe\n- Short columella\n- Deep philtrum\n- Constipation\n- Intellectual disability, moderate\n- Short nose\n- Depressed nasal bridge\n- Deviation of the hallux\n- Everted upper lip vermilion\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Short palpebral fissure\n- Colonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Hearing impairment\n- Absent earlobe\n- Narrow nasal bridge\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sacral dimple\n- Motor delay\n- Joint hypermobility\n- Selective tooth agenesis\n- Overlapping toe\n- Sandal gap\n- Deep philtrum\n- Intellectual disability, moderate\n- Sleep disturbance\n- Highly arched eyebrow\n- Duodenal ulcer\n- Delayed skeletal maturation\n- Recurrent upper respiratory tract infections\n- Decreased circulating antibody level\n- Depressed nasal bridge\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Prominent forehead\n- Broad thumb\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n- Fibular deviation of toes\n- Long fingers\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Hearing impairment\n- Absent earlobe\n- Narrow nasal bridge\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sacral dimple\n- Motor delay\n- Joint hypermobility\n- Selective tooth agenesis\n- Overlapping toe\n- Sandal gap\n- Deep philtrum\n- Intellectual disability, moderate\n- Sleep disturbance\n- Highly arched eyebrow\n- Duodenal ulcer\n- Delayed skeletal maturation\n- Recurrent upper respiratory tract infections\n- Decreased circulating antibody level\n- Depressed nasal bridge\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Prominent forehead\n- Broad thumb\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n- Fibular deviation of toes\n- Long fingers\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Hearing impairment\n- Absent earlobe\n- Narrow nasal bridge\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sacral dimple\n- Motor delay\n- Joint hypermobility\n- Selective tooth agenesis\n- Overlapping toe\n- Sandal gap\n- Deep philtrum\n- Intellectual disability, moderate\n- Sleep disturbance\n- Highly arched eyebrow\n- Duodenal ulcer\n- Delayed skeletal maturation\n- Recurrent upper respiratory tract infections\n- Decreased circulating antibody level\n- Depressed nasal bridge\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Prominent forehead\n- Broad thumb\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n- Fibular deviation of toes\n- Long fingers\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Hearing impairment\n- Absent earlobe\n- Narrow nasal bridge\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sacral dimple\n- Motor delay\n- Joint hypermobility\n- Selective tooth agenesis\n- Overlapping toe\n- Sandal gap\n- Deep philtrum\n- Intellectual disability, moderate\n- Sleep disturbance\n- Highly arched eyebrow\n- Duodenal ulcer\n- Delayed skeletal maturation\n- Recurrent upper respiratory tract infections\n- Decreased circulating antibody level\n- Depressed nasal bridge\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Prominent forehead\n- Broad thumb\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n- Fibular deviation of toes\n- Long fingers\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Microretrognathia\n- Low-set ears\n- Overfolded helix\n- Protruding ear\n- Telecanthus\n- Long eyelashes\n- Autistic behavior\n- Hypertrichosis\n- Obesity\n- Sandal gap\n- Frontal upsweep of hair\n- Intellectual disability, moderate\n- Postnatal growth retardation\n- Ulnar deviation of the 2nd finger\n- Deviation of the hallux\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Microretrognathia\n- Low-set ears\n- Overfolded helix\n- Protruding ear\n- Telecanthus\n- Long eyelashes\n- Autistic behavior\n- Hypertrichosis\n- Obesity\n- Sandal gap\n- Frontal upsweep of hair\n- Intellectual disability, moderate\n- Postnatal growth retardation\n- Ulnar deviation of the 2nd finger\n- Deviation of the hallux\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Microretrognathia\n- Low-set ears\n- Overfolded helix\n- Protruding ear\n- Telecanthus\n- Long eyelashes\n- Autistic behavior\n- Hypertrichosis\n- Obesity\n- Sandal gap\n- Frontal upsweep of hair\n- Intellectual disability, moderate\n- Postnatal growth retardation\n- Ulnar deviation of the 2nd finger\n- Deviation of the hallux\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Square face\n- Long philtrum\n- Low-set ears\n- Overfolded helix\n- Anteverted nares\n- Deeply set eye\n- Upslanted palpebral fissure\n- Prominent fingertip pads\n- Sandal gap\n- Short columella\n- Short nose\n- Depressed nasal bridge\n- Broad hallux\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Autistic behavior\n- Postnatal growth retardation\n- Broad hallux\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Microcephaly\n- Dolichocephaly\n- Epicanthus\n- Microretrognathia\n- Long philtrum\n- Low-set ears\n- Cupped ear\n- Protruding ear\n- Depressed nasal ridge\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Seizure\n- Intrauterine growth retardation\n- Frontal upsweep of hair\n- 2-3 toe cutaneous syndactyly\n- Postnatal growth retardation\n- Deviation of the hallux\n- Broad hallux\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Short philtrum\n- Strabismus\n- Deeply set eye\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypertrichosis\n- Sandal gap\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Multiple unerupted teeth\n- Postnatal growth retardation\n- Ulnar deviation of finger\n- Low hanging columella\n- Deviation of the hallux\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Short philtrum\n- Strabismus\n- Deeply set eye\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypertrichosis\n- Sandal gap\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Multiple unerupted teeth\n- Postnatal growth retardation\n- Ulnar deviation of finger\n- Low hanging columella\n- Deviation of the hallux\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Short philtrum\n- Strabismus\n- Deeply set eye\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypertrichosis\n- Sandal gap\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Multiple unerupted teeth\n- Postnatal growth retardation\n- Ulnar deviation of finger\n- Low hanging columella\n- Deviation of the hallux\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Short philtrum\n- Strabismus\n- Deeply set eye\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypertrichosis\n- Sandal gap\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Multiple unerupted teeth\n- Postnatal growth retardation\n- Ulnar deviation of finger\n- Low hanging columella\n- Deviation of the hallux\n- Cutaneous syndactyly of toes\n- Everted upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Full cheeks\n- Microretrognathia\n- Low-set ears\n- Cupped ear\n- Overfolded helix\n- Protruding ear\n- Strabismus\n- Telecanthus\n- Intellectual disability, mild\n- Sandal gap\n- Clinodactyly of the 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the urinary system\n- Microcephaly\n- Square face\n- Broad nasal tip\n- Anteverted nares\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Tapered finger\n- Seizure\n- Sandal gap\n- Short nose\n- Deviation of the hallux\n- Everted upper lip vermilion\n- Intellectual disability, severe\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Overfolded helix\n- Protruding ear\n- Broad nasal tip\n- Depressed nasal ridge\n- Anteverted nares\n- Telecanthus\n- Ptosis\n- Upslanted palpebral fissure\n- Intrauterine growth retardation\n- Short columella\n- Deep philtrum\n- Short nose\n- Deviation of the hallux\n- Flat face\n- Camptodactyly\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Cupped ear\n- Absent earlobe\n- Protruding ear\n- Broad nasal tip\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Upslanted palpebral fissure\n- Tapered finger\n- Prominent fingertip pads\n- Overlapping toe\n- Short columella\n- Intellectual disability, moderate\n- Scoliosis\n- Short nose\n- Ulnar deviation of finger\n- Deviation of the hallux\n- Flat face\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Cupped ear\n- Absent earlobe\n- Protruding ear\n- Broad nasal tip\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Upslanted palpebral fissure\n- Tapered finger\n- Prominent fingertip pads\n- Overlapping toe\n- Short columella\n- Intellectual disability, moderate\n- Scoliosis\n- Short nose\n- Ulnar deviation of finger\n- Deviation of the hallux\n- Flat face\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Cupped ear\n- Absent earlobe\n- Protruding ear\n- Broad nasal tip\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Upslanted palpebral fissure\n- Tapered finger\n- Prominent fingertip pads\n- Overlapping toe\n- Short columella\n- Intellectual disability, moderate\n- Scoliosis\n- Short nose\n- Ulnar deviation of finger\n- Deviation of the hallux\n- Flat face\n- Short palpebral fissure\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/02350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival overgrowth\n- High palate\n- Long face\n- Coarse facial features\n- Bulbous nose\n- Psychosis\n- Hypertrichosis\n- Intellectual disability, mild\n- Small nail\n- Absent toenail\n- Short toe\n- Intellectual disability, moderate\n- Increased body weight\n- Short finger\n- Short distal phalanx of finger\n- Thick vermilion border\n- Absent thumbnail\n- Absent fifth fingernail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival overgrowth\n- High palate\n- Long face\n- Coarse facial features\n- Bulbous nose\n- Psychosis\n- Hypertrichosis\n- Intellectual disability, mild\n- Small nail\n- Absent toenail\n- Short toe\n- Intellectual disability, moderate\n- Increased body weight\n- Short finger\n- Short distal phalanx of finger\n- Thick vermilion border\n- Absent thumbnail\n- Absent fifth fingernail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Strabismus\n- Deeply set eye\n- Nystagmus\n- Atypical behavior\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Dysarthria\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/02353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Gingival overgrowth\n- Coarse facial features\n- Low anterior hairline\n- Narrow forehead\n- Wide nasal bridge\n- Broad nasal tip\n- Hypermetropia\n- Thick eyebrow\n- Synophrys\n- Triphalangeal thumb\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Patent ductus arteriosus\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Long hallux\n- Short distal phalanx of toe\n- Polycythemia\n- Supernumerary nipple\n- Thoracolumbar kyphoscoliosis\n- Postnatal macrocephaly\n- Poor gross motor coordination\n- Short distal phalanx of finger\n- Thick nasal alae\n- Short 1st metacarpal\n- Hyperacusis\n- Prominent eyelashes\n- Absent hallux\n- Hypoplastic thumbnail\n- Wide nasal base\n- Clinodactyly\n- Long thumb\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Gingival overgrowth\n- Coarse facial features\n- Low anterior hairline\n- Narrow forehead\n- Wide nasal bridge\n- Broad nasal tip\n- Hypermetropia\n- Thick eyebrow\n- Synophrys\n- Triphalangeal thumb\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Patent ductus arteriosus\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Long hallux\n- Short distal phalanx of toe\n- Polycythemia\n- Supernumerary nipple\n- Thoracolumbar kyphoscoliosis\n- Postnatal macrocephaly\n- Poor gross motor coordination\n- Short distal phalanx of finger\n- Thick nasal alae\n- Short 1st metacarpal\n- Hyperacusis\n- Prominent eyelashes\n- Absent hallux\n- Hypoplastic thumbnail\n- Wide nasal base\n- Clinodactyly\n- Long thumb\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Long philtrum\n- Cupped ear\n- Protruding ear\n- Broad nasal tip\n- Long eyelashes\n- Synophrys\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Patent ductus arteriosus\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Facial hypertrichosis\n- Limb hypertonia\n- Increased body weight\n- Short finger\n- Joint contracture of the hand\n- Short distal phalanx of finger\n- Short distal phalanx of hallux\n- obsolete Toe walking\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Long philtrum\n- Cupped ear\n- Protruding ear\n- Broad nasal tip\n- Long eyelashes\n- Synophrys\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Patent ductus arteriosus\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Facial hypertrichosis\n- Limb hypertonia\n- Increased body weight\n- Short finger\n- Joint contracture of the hand\n- Short distal phalanx of finger\n- Short distal phalanx of hallux\n- obsolete Toe walking\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Deeply set eye\n- Aggressive behavior\n- Low frustration tolerance\n- Delayed speech and language development\n- Seizure\n- Ataxia\n- Intellectual disability, mild\n- Dysmetria\n- Limited elbow extension\n- Ventriculomegaly\n- Limited knee flexion\/extension\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/02358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Atypical behavior\n- Specific learning disability\n- Ventriculomegaly\n- Speech apraxia\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/02359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Pointed chin\n- Strabismus\n- Short attention span\n- Anxiety\n- Low frustration tolerance\n- Delayed speech and language development\n- Seizure\n- Ataxia\n- Intellectual disability, moderate\n- Abnormality of the palpebral fissures\n- Delayed fine motor development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/02360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Wide mouth\n- Thin upper lip vermilion\n- Retrognathia\n- Pointed chin\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Hypotonia\n- Intellectual disability, mild\n- Joint hypermobility\n- Pes planus\n- Clinodactyly of the 5th toe\n- Dysphagia\n- Migraine\n- Inverted nipples\n- Mild short stature\n- Low hanging columella\n- Long fingers\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Pointed chin\n- Hypertelorism\n- Prominent nasal bridge\n- Broad nasal tip\n- Ptosis\n- Autistic behavior\n- Delayed speech and language development\n- Congenital diaphragmatic hernia\n- Global developmental delay\n- Umbilical hernia\n- Ventricular septal defect\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Dyslexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Pointed chin\n- Hypertelorism\n- Hearing impairment\n- Prominent nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Attention deficit hyperactivity disorder\n- Attached earlobe\n- Dyslexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Pointed chin\n- Broad nasal tip\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Autistic behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Joint hypermobility\n- Obesity\n- Umbilical hernia\n- Short foot\n- Sandal gap\n- Vomiting\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Short stature\n- Attention deficit hyperactivity disorder\n- Low hanging columella\n- Feeding difficulties\n- Hodgkin lymphoma\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Aggressive behavior\n- Delayed speech and language development\n- Hypopigmentation of the skin\n- Intellectual disability\n- Motor delay\n- Joint hypermobility\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Hypoplastic nasal bridge\n- Retrocerebellar cyst\n- Long toe\n- Long fingers\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Wide mouth\n- Thin upper lip vermilion\n- Pointed chin\n- Posteriorly rotated ears\n- Broad nasal tip\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Scoliosis\n- Short stature\n- Thick corpus callosum\n- Feeding difficulties in infancy\n- Low hanging columella\n- Narrow palpebral fissure\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Pointed chin\n- Broad nasal tip\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Hemiparesis\n- Motor delay\n- Obesity\n- Short foot\n- Intellectual disability, moderate\n- Scoliosis\n- Short palm\n- Short stature\n- Feeding difficulties in infancy\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Oligospermia\n- Intellectual disability, mild\n- Motor delay\n- Short stature\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/02368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Cleft palate\n- Lobulated tongue\n- Accessory oral frenulum\n- Short lingual frenulum\n- Gingival overgrowth\n- Delayed eruption of teeth\n- Syndactyly\n- Postaxial hand polydactyly\n- Hypotonia\n- Generalized hypotonia\n- Absent speech\n- Bifid distal phalanx of toe\n- Ventriculomegaly\n- Molar tooth sign on MRI\n- Short stature\n- Decreased body weight\n- Persistent open anterior fontanelle\n- Partial duplication of the distal phalanx of the hallux\n- Hamartoma of tongue\n- Nasogastric tube feeding\n- Preaxial polydactyly\n- Mesoaxial polydactyly\n- Agenesis of maxillary incisor\n- Agenesis of mandibular incisor\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/02369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Lobulated tongue\n- High palate\n- Short neck\n- Global developmental delay\n- Small for gestational age\n- Bilateral talipes equinovarus\n- Preaxial foot polydactyly\n- Frontal bossing\n- Dyspnea\n- Tachypnea\n- Thoracic kyphosis\n- Mesoaxial hand polydactyly\n- Axial hypotonia\n- Radial deviation of the hand or of fingers of the hand\n- Partial duplication of the distal phalanx of the hallux\n- Polydactyly\n- Abnormality of the hypothenar eminence\n- Abnormality of the palmar creases\n- Cutaneous finger syndactyly\n- Intracranial cystic lesion\n- Broad thumb\n- Systolic heart murmur\n- Agenesis of mandibular incisor\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/02370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Lobulated tongue\n- Carious teeth\n- Hand polydactyly\n- Foot polydactyly\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/02371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Lobulated tongue\n- Accessory oral frenulum\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Absent speech\n- Bilateral talipes equinovarus\n- Poor head control\n- Bilateral cleft lip and palate\n- Atrioventricular canal defect\n- Aplasia of the epiglottis\n- Metacarpal synostosis\n- Polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/02372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Lobulated tongue\n- Hypertelorism\n- Agenesis of corpus callosum\n- Dandy-Walker malformation\n- Cerebellar hypoplasia\n- Calvarial skull defect\n- Atrial septal defect\n- Patent foramen ovale\n- Encephalocele\n- Meningocele\n- Bilateral cleft lip and palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/02375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/02382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Hypotonia\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormal palate morphology\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Vitiligo\n- Hypotonia\n- Failure to thrive\n- Poor suck\n- Intellectual disability, moderate\n- Abnormal 5th finger morphology\n- Abnormal fifth toe morphology\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Anteverted nares\n- Atypical behavior\n- Delayed speech and language development\n- Eczema\n- Hypertrichosis\n- Hypotonia\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Scoliosis\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormal palate morphology\n- Ptosis\n- Long eyelashes\n- Thick eyebrow\n- Atypical behavior\n- Delayed speech and language development\n- Hypertrichosis\n- Hypotonia\n- Intellectual disability, mild\n- Failure to thrive\n- Poor suck\n- Abnormal 5th finger morphology\n- Feeding difficulties in infancy\n- Abnormal fifth toe morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Hypotonia\n- Poor suck\n- Abnormality of speech or vocalization\n- Feeding difficulties in infancy\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thick eyebrow\n- Atypical behavior\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Absent speech\n- Kyphosis\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Thick lower lip vermilion\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Atypical behavior\n- Seizure\n- Hypotonia\n- Absent speech\n- Failure to thrive\n- Poor suck\n- Scoliosis\n- CNS hypomyelination\n- Aortic aneurysm\n- Generalized cerebral atrophy\/hypoplasia\n- Feeding difficulties in infancy\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin upper lip vermilion\n- Atypical behavior\n- Hypotonia\n- Absent speech\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Small forehead\n- Thickened helices\n- Prominent nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Brachydactyly\n- Seizure\n- Cerebellar atrophy\n- Short toe\n- Bilateral tonic-clonic seizure\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Genu valgum\n- Increased body weight\n- Prominent nasal tip\n- Myoclonic absence seizure\n- Hyperpyrexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/02391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long face\n- Small forehead\n- Thickened helices\n- Prominent nasal bridge\n- Short neck\n- Thick eyebrow\n- Atypical behavior\n- Abnormality of the skeletal system\n- Brachydactyly\n- Seizure\n- Short toe\n- Bilateral tonic-clonic seizure\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Genu valgum\n- Prominent nasal tip\n- Myoclonic absence seizure\n- Hyperpyrexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/02392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypospadias\n- High palate\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Protruding ear\n- Anteverted nares\n- Exotropia\n- Delayed speech and language development\n- Motor delay\n- Pes planus\n- Talipes equinovalgus\n- Cerebral cortical atrophy\n- Scoliosis\n- Kyphosis\n- Short nose\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Prolonged neonatal jaundice\n- Lower limb hypertonia\n- Tented upper lip vermilion\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/02393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Everted lower lip vermilion\n- Dolichocephaly\n- Facial hypotonia\n- Macrotia\n- Short neck\n- Hypotelorism\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hallux valgus\n- Thoracic scoliosis\n- Clinodactyly of the 5th finger\n- Short palm\n- Increased body weight\n- 2-3 toe syndactyly\n- Abnormality of brain morphology\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Hypertelorism\n- Abnormality of the eye\n- Downslanted palpebral fissures\n- Glaucoma\n- Proptosis\n- Atypical behavior\n- Abnormal thorax morphology\n- Abnormal sternum morphology\n- Pectus excavatum\n- Abnormality of the skeletal system\n- Intellectual disability\n- Motor delay\n- Joint hypermobility\n- Joint laxity\n- Abnormal heart morphology\n- Hammertoe\n- Broad nail\n- Incoordination\n- Short 5th finger\n- Short 5th toe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Hearing impairment\n- Abnormality of the eye\n- Atypical behavior\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Short neck\n- Epicanthus inversus\n- Hypermetropia\n- Blepharophimosis\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Bradycardia\n- Autoimmune thrombocytopenia\n- Large forehead\n- Gastroesophageal reflux\n- Respiratory distress\n- 2-3 toe syndactyly\n- Prominent metopic ridge\n- Congenital sensorineural hearing impairment\n- Axial hypotonia\n- Sleep apnea\n- Feeding difficulties\n- Chronic constipation\n- Widened subarachnoid space\n- Insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Bifid uvula\n- High palate\n- Microcephaly\n- Triangular face\n- Broad forehead\n- Cupped ear\n- Small earlobe\n- Protruding ear\n- Anteverted nares\n- Abnormality of the eye\n- Thick eyebrow\n- Nasolacrimal duct obstruction\n- Long palpebral fissure\n- Dental crowding\n- Atypical behavior\n- Delayed speech and language development\n- Abnormal thorax morphology\n- Hyperkeratosis\n- Prominent fingertip pads\n- Intellectual disability\n- Motor delay\n- Small for gestational age\n- Short toe\n- Genu valgum\n- Short nose\n- Decreased body weight\n- Depressed nasal bridge\n- Prominent proximal interphalangeal joints\n- Attention deficit hyperactivity disorder\n- Microtia\n- Short 5th finger\n- Short thumb\n- Cone-shaped epiphysis\n- Broad columella\n- Broad eyebrow\n- Feeding difficulties\n- High insertion of columella\n- Wide nasal base\n- Clinodactyly\n- Grade III vesicoureteral reflux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Motor delay\n- Absent speech\n- Joint hypermobility\n- Small for gestational age\n- Severe global developmental delay\n- Feeding difficulties\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Hypertelorism\n- Narrow forehead\n- Macrotia\n- Protruding ear\n- Anteverted nares\n- Abnormality of the eye\n- Atypical behavior\n- Delayed speech and language development\n- Hypertension\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Oligohydramnios\n- Exaggerated cupid's bow\n- Highly arched eyebrow\n- Long eyebrows\n- Sparse hair\n- Maternal diabetes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Tall stature\n- Abnormality of the genitourinary system\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hearing impairment\n- Abnormality of the eye\n- Ptosis\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Joint hypermobility\n- Expressive language delay\n- Short stature\n- Bilateral conductive hearing impairment\n- Midface retrusion\n- Abnormality of brain morphology\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Retinal coloboma\n- Optic nerve hypoplasia\n- Delayed speech and language development\n- Intellectual disability\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Abnormality of the genitourinary system\n- Hydrocephalus\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Myelomeningocele\n- Skeletal muscle atrophy\n- Short stature\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Retrognathia\n- Epicanthus\n- Microretrognathia\n- Sensorineural hearing impairment\n- Blepharophimosis\n- Autistic behavior\n- Delayed speech and language development\n- Brachydactyly\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Joint hypermobility\n- Intrauterine growth retardation\n- Small for gestational age\n- Oligohydramnios\n- Talipes equinovarus\n- Lower limb spasticity\n- Short stature\n- 2-3 toe syndactyly\n- Prominent nasal tip\n- Intellectual disability, severe\n- Feeding difficulties\n- Abnormality of brain morphology\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Torticollis\n- Abnormality of the eye\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Abnormal heart morphology\n- Obstructive sleep apnea\n- Easy fatigability\n- Abnormality of brain morphology\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Abnormality of the genitourinary system\n- Narrow nasal bridge\n- Atypical behavior\n- Delayed speech and language development\n- Tapered finger\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Small for gestational age\n- Long hallux\n- Unsteady gait\n- Increased body weight\n- 2-3 toe syndactyly\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Broad-based gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/02408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Brachycephaly\n- Microcephaly\n- Epicanthus\n- Posteriorly rotated ears\n- Anteverted nares\n- Strabismus\n- Keratoconus\n- Seizure\n- Intellectual disability, mild\n- Generalized hypotonia\n- Ventricular septal defect\n- Constipation\n- Delayed CNS myelination\n- Short nose\n- Clinodactyly of the 5th finger\n- Feeding difficulties\n- Stellate iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Malar flattening\n- Posteriorly rotated ears\n- Anteverted nares\n- Deeply set eye\n- Specific learning disability\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Camptodactyly\n- Thick vermilion border\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Wide nasal bridge\n- Telecanthus\n- Lacrimal duct atresia\n- Ectropion\n- Global developmental delay\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Wide nasal bridge\n- Global developmental delay\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Upslanted palpebral fissure\n- Global developmental delay\n- Low hanging columella\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Anteverted nares\n- Telecanthus\n- Single transverse palmar crease\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Anteverted nares\n- Telecanthus\n- Single transverse palmar crease\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Anteverted nares\n- Telecanthus\n- Single transverse palmar crease\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal insufficiency\n- Wide nasal bridge\n- Deeply set eye\n- Hypothyroidism\n- Adrenal insufficiency\n- Global developmental delay\n- Supraventricular tachycardia\n- Laryngotracheomalacia\n- Sparse eyebrow\n- Type I diabetes mellitus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Mandibular prognathia\n- Global developmental delay\n- Supernumerary nipple\n- Median cleft lip and palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Mandibular prognathia\n- Global developmental delay\n- Supernumerary nipple\n- Median cleft lip and palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Mandibular prognathia\n- Global developmental delay\n- Supernumerary nipple\n- Median cleft lip and palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- Epicanthus\n- Global developmental delay\n- Highly arched eyebrow\n- Depressed nasal bridge\n- Prominent forehead\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Global developmental delay\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Low-set ears\n- Telecanthus\n- Global developmental delay\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Optic disc coloboma\n- Global developmental delay\n- Lacrimal duct aplasia\n- Blepharochalasis\n- Sparse medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Optic disc coloboma\n- Global developmental delay\n- Lacrimal duct aplasia\n- Blepharochalasis\n- Sparse medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Macrocephaly\n- Dolichocephaly\n- Long face\n- Coarse facial features\n- Autism\n- Hypertrichosis\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Hip dysplasia\n- Large for gestational age\n- Pes planus\n- Constipation\n- Gastroesophageal reflux\n- Scoliosis\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- Severe global developmental delay\n- Thick hair\n- Lateral ventricular asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Renal cyst\n- Macroglossia\n- Gingival overgrowth\n- Microcephaly\n- Seizure\n- Hypotonia\n- Large for gestational age\n- Intellectual disability, profound\n- Highly arched eyebrow\n- Thoracic scoliosis\n- Short stature\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Gingival overgrowth\n- Thick upper lip vermilion\n- Macrocephaly\n- Low anterior hairline\n- Thickened helices\n- Bulbous nose\n- Prominent nose\n- Myopia\n- Thick eyebrow\n- Oculomotor apraxia\n- Dental malocclusion\n- Hypertrichosis\n- Ataxia\n- Intellectual disability, mild\n- Intention tremor\n- Clumsiness\n- Scoliosis\n- Increased body weight\n- Focal-onset seizure\n- Few cafe-au-lait spots\n- Asymmetric growth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Global developmental delay\n- Short palpebral fissure\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Turricephaly\n- Facial hypotonia\n- Long philtrum\n- Long eyelashes\n- Pectus carinatum\n- Hirsutism\n- Seizure\n- Hypotonia\n- Motor delay\n- Bilateral ptosis\n- Anonychia\n- Short nail\n- Constipation\n- Truncal ataxia\n- Highly arched eyebrow\n- Thoracic kyphosis\n- Skeletal muscle atrophy\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- Protruding tongue\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Global developmental delay\n- Short palpebral fissure\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Deeply set eye\n- Upslanted palpebral fissure\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Deeply set eye\n- Upslanted palpebral fissure\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Global developmental delay\n- Wide nasal ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/02435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroorchidism\n- Macroglossia\n- Gingival overgrowth\n- Coarse facial features\n- Bulbous nose\n- Prominent nose\n- Bifid nasal tip\n- Synophrys\n- Hypotonia\n- Global developmental delay\n- Encephalopathy\n- Anonychia\n- Kyphosis\n- Hyperlordosis\n- Pes valgus\n- Aplasia of the distal phalanges of the hand\n- Unilateral deafness\n- Aplasia of the distal phalanges of the toes\n- Intellectual disability, severe\n- Thick vermilion border\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/02436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Glabellar hemangioma\n- Polyhydramnios\n- Supravalvular aortic stenosis\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/02437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival overgrowth\n- Macrocephaly\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Myopia\n- Delayed eruption of teeth\n- Decreased response to growth hormone stimulation test\n- Motor delay\n- Specific learning disability\n- Failure to thrive\n- Polyhydramnios\n- Ventricular septal defect\n- Lymphopenia\n- Ventriculomegaly\n- Chiari malformation\n- Feeding difficulties\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/02438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Ventricular septal defect\n- Partially duplicated kidney\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/02439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Ventricular septal defect\n- Partially duplicated kidney\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/02440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Downslanted palpebral fissures\n- Delayed puberty\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/02441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Hearing impairment\n- Wide nasal bridge\n- Visual impairment\n- Hypothyroidism\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Areflexia\n- Constipation\n- Recurrent respiratory infections\n- Spastic\/hyperactive bladder\n- Equinovarus deformity\n- Uplifted earlobe\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/02442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Downslanted palpebral fissures\n- Delayed puberty\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/02443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Overfolded helix\n- Wide nasal bridge\n- Visual impairment\n- Optic disc pallor\n- Single transverse palmar crease\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Areflexia\n- Exocrine pancreatic insufficiency\n- Constipation\n- Hepatomegaly\n- Axonal loss\n- Sensorimotor neuropathy\n- Protruding tongue\n- Fetal pyelectasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/02444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Retrognathia\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Bulbous nose\n- Wide nasal bridge\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Reduced tendon reflexes\n- Failure to thrive\n- Left ventricular hypertrophy\n- Small nail\n- Pneumonia\n- Pulmonary arterial hypertension\n- Respiratory insufficiency\n- Sudden episodic apnea\n- Elevated circulating alkaline phosphatase concentration\n- Shortening of all distal phalanges of the fingers\n- Lateral ventricle dilatation\n- Undetectable visual evoked potentials\n- Gastrostomy tube feeding in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/02445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micropenis\n- Thin upper lip vermilion\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Short chin\n- Long philtrum\n- Overfolded helix\n- Wide nose\n- Epicanthus inversus\n- Long palpebral fissure\n- Brachydactyly\n- Seizure\n- Dandy-Walker malformation\n- Cerebellar vermis hypoplasia\n- Absent toenail\n- Short columella\n- Polymicrogyria\n- Complex palmar dermatoglyphic pattern\n- Large earlobe\n- Broad eyebrow\n- Hypoplasia of the pons\n- Absent fifth fingernail\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/02446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Pointed chin\n- Smooth philtrum\n- Long philtrum\n- Hearing impairment\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Lethargy\n- Global developmental delay\n- Small nail\n- Short toe\n- Fever\n- Constipation\n- Poor suck\n- Facial hypertrichosis\n- Elevated circulating alkaline phosphatase concentration\n- Prominent nasal tip\n- Sensorimotor neuropathy\n- Short 5th finger\n- Aplasia of the distal phalanges of the hand\n- Uplifted earlobe\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- EEG with burst suppression\n- Chin with horizontal crease\n- Feeding difficulties\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/02447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Pointed chin\n- Smooth philtrum\n- Long philtrum\n- Hearing impairment\n- Macrotia\n- Thickened nuchal skin fold\n- Hypertrichosis\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Polyneuropathy\n- Protuberant abdomen\n- Polyhydramnios\n- Small nail\n- Short toe\n- Poor suck\n- Ventriculomegaly\n- Elevated circulating alkaline phosphatase concentration\n- Hypoplastic spleen\n- Neck muscle hypoplasia\n- Short 5th finger\n- Aplasia of the distal phalanx of the 5th finger\n- Uplifted earlobe\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- Chin with horizontal crease\n- Premature skin wrinkling\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/02448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Horizontal nystagmus\n- Hypotonia\n- Global developmental delay\n- Truncal ataxia\n- Cerebellar vermis atrophy\n- Delayed ability to walk\n- Paroxysmal tonic upgaze\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/02449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gaze-evoked nystagmus\n- Hypotonia\n- Limb ataxia\n- Truncal ataxia\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/02450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Oculomotor apraxia\n- Horizontal nystagmus\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Hyperreflexia\n- Limb ataxia\n- Truncal ataxia\n- Vertical nystagmus\n- Delayed ability to stand\n- Delayed ability to sit\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/02451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Oculomotor apraxia\n- Horizontal nystagmus\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Hyperreflexia\n- Limb ataxia\n- Truncal ataxia\n- Scoliosis\n- Thoracolumbar kyphosis\n- Vertical nystagmus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/02452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long eyelashes\n- Delayed speech and language development\n- Hirsutism\n- Global developmental delay\n- Specific learning disability\n- Overlapping toe\n- Postural instability\n- Recurrent respiratory infections\n- Highly arched eyebrow\n- Aspiration\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Broad distal phalanx of the thumb\n- Low hanging columella\n- Broad distal phalanx of finger\n- Delayed fine motor development\n- Nasogastric tube feeding in infancy\n- Tufted hairs\n- Abnormality of the tympanic membrane\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long eyelashes\n- Delayed speech and language development\n- Hirsutism\n- Global developmental delay\n- Specific learning disability\n- Overlapping toe\n- Postural instability\n- Recurrent respiratory infections\n- Highly arched eyebrow\n- Aspiration\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Broad distal phalanx of the thumb\n- Low hanging columella\n- Broad distal phalanx of finger\n- Delayed fine motor development\n- Nasogastric tube feeding in infancy\n- Tufted hairs\n- Abnormality of the tympanic membrane\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Myopia\n- Carious teeth\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Specific learning disability\n- Ventricular septal defect\n- Dysphagia\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Genu valgum\n- Pes valgus\n- Broad hallux\n- Increased overbite\n- Broad thumb\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Myopia\n- Carious teeth\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Specific learning disability\n- Ventricular septal defect\n- Dysphagia\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Genu valgum\n- Pes valgus\n- Broad hallux\n- Increased overbite\n- Broad thumb\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Myopia\n- Carious teeth\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Specific learning disability\n- Ventricular septal defect\n- Dysphagia\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Genu valgum\n- Pes valgus\n- Broad hallux\n- Increased overbite\n- Broad thumb\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Retrognathia\n- Protruding ear\n- Short attention span\n- Delayed speech and language development\n- Jaundice\n- Hypotonia\n- Motor delay\n- Plagiocephaly\n- Neonatal hypoglycemia\n- Highly arched eyebrow\n- Flat occiput\n- Broad hallux\n- Broad thumb\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n- Long eyelashes\n- Blue irides\n- Hypotonia\n- Joint laxity\n- Hypoplastic toenails\n- Delayed gross motor development\n- Sleep disturbance\n- Mild short stature\n- Prolonged neonatal jaundice\n- Few cafe-au-lait spots\n- Feeding difficulties in infancy\n- Head-banging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Anteverted nares\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Single transverse palmar crease\n- Soft skin\n- Tapered finger\n- Slender finger\n- Global developmental delay\n- Joint laxity\n- Sandal gap\n- Difficulty climbing stairs\n- Decreased body weight\n- Coronal hypospadias\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Thin vermilion border\n- Epicanthus\n- Prominent nasal bridge\n- Strabismus\n- Upslanted palpebral fissure\n- Tapered finger\n- Slender finger\n- Seizure\n- Global developmental delay\n- Plagiocephaly\n- Joint laxity\n- Pes planus\n- Sandal gap\n- Recurrent upper respiratory tract infections\n- Clinodactyly of the 5th finger\n- Attention deficit hyperactivity disorder\n- Attached earlobe\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Broad philtrum\n- Microretrognathia\n- Bulbous nose\n- Underdeveloped nasal alae\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Irritability\n- Delayed speech and language development\n- Reduced eye contact\n- Brachydactyly\n- Vomiting\n- Constipation\n- Sleep disturbance\n- Recurrent upper respiratory tract infections\n- Short stature\n- Attention deficit hyperactivity disorder\n- Pain insensitivity\n- Midface retrusion\n- Abnormal temper tantrums\n- Overweight\n- Cerebral visual impairment\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Microretrognathia\n- High forehead\n- Bulbous nose\n- Underdeveloped nasal alae\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Brachydactyly\n- Motor delay\n- Plagiocephaly\n- Joint laxity\n- Obesity\n- Broad foot\n- Thin nail\n- Poor suck\n- Short nose\n- Short middle phalanx of the 5th finger\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Axial hypotonia\n- Short middle phalanx of the 2nd finger\n- Broad hallux\n- Abnormality of pain sensation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Smooth philtrum\n- Anxiety\n- Prominent fingertip pads\n- Global developmental delay\n- Obesity\n- Highly arched eyebrow\n- Short palm\n- Increased body weight\n- Deep palmar crease\n- Low hanging columella\n- Nasal regurgitation\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Coarse facial features\n- Deeply set eye\n- Hypotelorism\n- Osteopenia\n- Soft skin\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Photosensitive myoclonic seizure\n- Failure to thrive\n- Short foot\n- Gait ataxia\n- Broad-based gait\n- Unsteady gait\n- Sleep disturbance\n- Highly arched eyebrow\n- Polyphagia\n- Prominent nasal tip\n- Sparse hair\n- Tapered toe\n- Short digit\n- Feeding difficulties\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow palate\n- Epicanthus\n- Protruding ear\n- Jaundice\n- Eczema\n- Global developmental delay\n- Obesity\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Genu valgum\n- Attention deficit hyperactivity disorder\n- Gait apraxia\n- Sleep apnea\n- Choking episodes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Cupped ear\n- Wide nasal bridge\n- Ptosis\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability, mild\n- Global developmental delay\n- Small nail\n- Intellectual disability, moderate\n- Short stature\n- Polysyndactyly of hallux\n- Congenital bilateral ptosis\n- Hypoplastic helices\n- Short 5th finger\n- Overweight\n- Clinodactyly\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Functional abnormality of the bladder\n- Urinary retention\n- Macroorchidism\n- Atypical behavior\n- Autism\n- Aggressive behavior\n- Impaired social interactions\n- Low frustration tolerance\n- Delayed speech and language development\n- Enuresis\n- Seizure\n- Polydipsia\n- Constipation\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydronephrosis\n- Trigonocephaly\n- Microcephaly\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Narrow forehead\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Macrotia\n- Wide nasal bridge\n- Anteverted nares\n- Torticollis\n- Strabismus\n- Ptosis\n- Shallow orbits\n- Long palpebral fissure\n- Synophrys\n- Hemangioma\n- Tapered finger\n- Global developmental delay\n- Hypertonia\n- Plagiocephaly\n- Craniosynostosis\n- Failure to thrive\n- Intrauterine growth retardation\n- Patent foramen ovale\n- Secundum atrial septal defect\n- Left ventricular hypertrophy\n- Small nail\n- Constipation\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Deep palmar crease\n- Short finger\n- Increased nuchal translucency\n- Feeding difficulties\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Submucous cleft hard palate\n- Bifid uvula\n- Low anterior hairline\n- Mandibular prognathia\n- Macrotia\n- Depressed nasal ridge\n- Strabismus\n- Oculomotor apraxia\n- Inappropriate laughter\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Polyhydramnios\n- Expressive language delay\n- Deviated nasal septum\n- Flat occiput\n- Increased nuchal translucency\n- Wide nasal ridge\n- Tibial torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Small forehead\n- Macrotia\n- Bulbous nose\n- Long eyelashes\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Anxiety\n- Delayed speech and language development\n- Specific learning disability\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Thick upper lip vermilion\n- Epicanthus\n- Short philtrum\n- Protruding ear\n- Hypotelorism\n- Delayed speech and language development\n- Hyperactivity\n- Abnormal foot morphology\n- Tracheomalacia\n- Attention deficit hyperactivity disorder\n- Prominent forehead\n- Feeding difficulties\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hydrocephalus\n- Low anterior hairline\n- Hypertelorism\n- Long eyelashes\n- Upslanted palpebral fissure\n- Amblyopia\n- Delayed speech and language development\n- Hypertrichosis\n- Intellectual disability, mild\n- Global developmental delay\n- Joint laxity\n- Hypernasal speech\n- Pes planus\n- Vomiting\n- Scoliosis\n- Long nose\n- Short stature\n- Multiple cafe-au-lait spots\n- Progressive congenital scoliosis\n- Broad hallux\n- Feeding difficulties\n- Weakness of facial musculature\n- Narrow palpebral fissure\n- Chiari type II malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/02474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Low anterior hairline\n- Narrow forehead\n- Long philtrum\n- Bulbous nose\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Irritability\n- Anxiety\n- Delayed speech and language development\n- Decreased response to growth hormone stimulation test\n- Hypertrichosis\n- Tapered finger\n- Global developmental delay\n- Bilateral ptosis\n- Growth delay\n- Ventricular septal defect\n- Thrombocytopenia\n- Leukopenia\n- Constipation\n- Short stature\n- Short finger\n- Short 3rd finger\n- Thick vermilion border\n- Systolic heart murmur\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/02475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Macrocephaly\n- Round face\n- Long philtrum\n- Low-set ears\n- Preauricular skin tag\n- Bulbous nose\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Tapered finger\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Short stature\n- Preauricular pit\n- Short finger\n- Short 3rd finger\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/02476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Round face\n- Long philtrum\n- Prominent antihelix\n- Bulbous nose\n- Anteverted nares\n- Hyperopic astigmatism\n- Downslanted palpebral fissures\n- Tapered finger\n- Global developmental delay\n- Short finger\n- High anterior hairline\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/02477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Wide nasal bridge\n- Delayed speech and language development\n- Hirsutism\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Joint laxity\n- Coxa valga\n- Delayed skeletal maturation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/02478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hearing impairment\n- Atypical behavior\n- Hypotonia\n- Cerebellar atrophy\n- Partial agenesis of the corpus callosum\n- Absent speech\n- Pulmonic stenosis\n- Sleep disturbance\n- Short stature\n- Decreased body weight\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/02479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Narrow mouth\n- Abnormality of the dentition\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Hearing impairment\n- Blepharophimosis\n- Osteopenia\n- Cyanosis\n- Syndactyly\n- Global developmental delay\n- Neonatal hypotonia\n- Abnormal heart morphology\n- Eosinophilia\n- Respiratory distress\n- Recurrent respiratory infections\n- Abnormal tracheal morphology\n- Hypoalbuminemia\n- Decreased circulating antibody level\n- Short stature\n- Decreased body weight\n- Recurrent infection of the gastrointestinal tract\n- Depressed nasal bridge\n- Generalized edema\n- Microtia\n- Feeding difficulties\n- Camptodactyly\n- Lymphoid nodular hyperplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/02480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Narrow mouth\n- Abnormality of the dentition\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Hearing impairment\n- Blepharophimosis\n- Osteopenia\n- Cyanosis\n- Syndactyly\n- Global developmental delay\n- Neonatal hypotonia\n- Abnormal heart morphology\n- Eosinophilia\n- Respiratory distress\n- Recurrent respiratory infections\n- Abnormal tracheal morphology\n- Hypoalbuminemia\n- Decreased circulating antibody level\n- Short stature\n- Decreased body weight\n- Recurrent infection of the gastrointestinal tract\n- Depressed nasal bridge\n- Generalized edema\n- Microtia\n- Feeding difficulties\n- Camptodactyly\n- Lymphoid nodular hyperplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/02481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/02523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Tall stature\n- Thick lower lip vermilion\n- Macrocephaly\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Gynecomastia\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Scoliosis\n- Downturned corners of mouth\n- Inverted nipples\n- Increased body weight\n- Postnatal macrocephaly\n- Accelerated skeletal maturation\n- Prominent forehead\n- Premature pubarche\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Obesity\n- Atrial septal defect\n- Sandal gap\n- Sleep disturbance\n- Inverted nipples\n- Increased body weight\n- Postnatal macrocephaly\n- Accelerated skeletal maturation\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Obesity\n- Atrial septal defect\n- Sandal gap\n- Sleep disturbance\n- Inverted nipples\n- Increased body weight\n- Postnatal macrocephaly\n- Accelerated skeletal maturation\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal duplication\n- Coarse facial features\n- Wide nasal bridge\n- Long eyelashes\n- Abnormality of the nervous system\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Atrial septal defect\n- Tented upper lip vermilion\n- Coronary artery aneurysm\n- Nocturnal seizures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Motor delay\n- Sleep disturbance\n- Attention deficit hyperactivity disorder\n- Abnormal hair whorl\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Long philtrum\n- Deeply set eye\n- Autistic behavior\n- Intellectual disability\n- Spasticity\n- Motor delay\n- Generalized hypotonia\n- Sleep disturbance\n- Severe expressive language delay\n- Tented upper lip vermilion\n- Severe receptive language delay\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Long philtrum\n- Deeply set eye\n- Autistic behavior\n- Intellectual disability\n- Spasticity\n- Motor delay\n- Generalized hypotonia\n- Sleep disturbance\n- Severe expressive language delay\n- Tented upper lip vermilion\n- Severe receptive language delay\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Plagiocephaly\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Aggressive behavior\n- Autistic behavior\n- Hyperactivity\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Sleep disturbance\n- Severe expressive language delay\n- Tented upper lip vermilion\n- Severe receptive language delay\n- Midface retrusion\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Brachycephaly\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Seizure\n- Motor delay\n- High pitched voice\n- Paroxysmal dyskinesia\n- Ichthyosis\n- Joint contracture of the 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Hypohidrosis\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Sleep disturbance\n- Severe expressive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Sleep disturbance\n- Scoliosis\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Sleep disturbance\n- Scoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Motor delay\n- Generalized hypotonia\n- Overgrowth\n- Postural instability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Renal cyst\n- Macrocephaly\n- Abnormality of vision\n- Long eyelashes\n- Autistic behavior\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Dysphagia\n- Gastroesophageal reflux\n- Lower limb spasticity\n- Sleep disturbance\n- Cavum septum pellucidum\n- Severe expressive language delay\n- Severe receptive language delay\n- Midface retrusion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Autistic behavior\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Muscle weakness\n- Abnormality of the immune system\n- Attention deficit hyperactivity disorder\n- Delayed social development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Aggressive behavior\n- Anxiety\n- Intellectual disability\n- Global developmental delay\n- Specific learning disability\n- Tremor\n- Brisk reflexes\n- Pes planus\n- Incoordination\n- Obsessive-compulsive trait\n- Abnormality of the gastrointestinal tract\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Myopia\n- Keratoconus\n- Autistic behavior\n- Anxiety\n- Reduced eye contact\n- Intellectual disability\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Tremor\n- Brisk reflexes\n- Pes planus\n- Constipation\n- Migraine\n- Incoordination\n- Scoliosis\n- Abnormality of the immune system\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Pes valgus\n- Fatigue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Depression\n- Compulsive behaviors\n- Autistic behavior\n- Anxiety\n- Intellectual disability\n- Global developmental delay\n- Abnormality of the gastrointestinal tract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/02542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Renal agenesis\n- Hearing impairment\n- Visual impairment\n- Hypotonia\n- Absent speech\n- Joint hypermobility\n- Dysphagia\n- Gastroesophageal reflux\n- Poor head control\n- Scoliosis\n- High, narrow palate\n- Infantile muscular hypotonia\n- Overlapping fingers\n- Increased nuchal translucency\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Cryptorchidism\n- Hydroureter\n- Vesicoureteral reflux\n- Cleft palate\n- Hearing impairment\n- Hypotonia\n- Global developmental delay\n- Hip dysplasia\n- Oligohydramnios\n- Abnormal heart morphology\n- Atrial septal defect\n- Gastroesophageal reflux\n- Obstructive sleep apnea\n- Infantile muscular hypotonia\n- Overlapping fingers\n- Aplasia of the falx cerebri\n- Interictal epileptiform activity\n- Perisylvian polymicrogyria\n- Necrotizing enterocolitis\n- Cerebral visual impairment\n- Thin corpus callosum\n- Dependency on parenteral nutrition\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Joint laxity\n- Dysphagia\n- Constipation\n- Infantile muscular hypotonia\n- Overlapping fingers\n- Severe global developmental delay\n- Otitis media with effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Seizure\n- Hypotonia\n- Absent speech\n- Ventricular septal defect\n- Atrial septal defect\n- Gastroesophageal reflux\n- Asthma\n- Inability to walk\n- Decreased body weight\n- Infantile muscular hypotonia\n- Abnormality of the palmar creases\n- Intellectual disability, severe\n- EEG with abnormally slow frequencies\n- Perisylvian polymicrogyria\n- Tube feeding\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Deeply set eye\n- Downslanted palpebral fissures\n- Long palpebral fissure\n- Hemangioma\n- Intellectual disability\n- Failure to thrive\n- Atrial septal defect\n- Gastroesophageal reflux\n- Abnormal cerebral white matter morphology\n- Eversion of lateral third of lower eyelids\n- Low hanging columella\n- Midface retrusion\n- Feeding difficulties\n- Choking episodes\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Deeply set eye\n- Downslanted palpebral fissures\n- Long palpebral fissure\n- Hemangioma\n- Intellectual disability\n- Failure to thrive\n- Atrial septal defect\n- Gastroesophageal reflux\n- Abnormal cerebral white matter morphology\n- Eversion of lateral third of lower eyelids\n- Low hanging columella\n- Midface retrusion\n- Feeding difficulties\n- Choking episodes\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Submucous cleft hard palate\n- Bifid uvula\n- Decreased response to growth hormone stimulation test\n- Intrauterine growth retardation\n- Small for gestational age\n- Submucous cleft soft palate\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Submucous cleft hard palate\n- Bifid uvula\n- Decreased response to growth hormone stimulation test\n- Intrauterine growth retardation\n- Small for gestational age\n- Submucous cleft soft palate\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Inguinal hernia\n- Tall stature\n- Mandibular prognathia\n- Macrotia\n- Broad nasal tip\n- Strabismus\n- Myopia\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability, mild\n- Obesity\n- Umbilical hernia\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Phimosis\n- Pes planus\n- Short toe\n- Polyphagia\n- Increased body weight\n- Descending thoracic aorta aneurysm\n- Attention deficit hyperactivity disorder\n- Few cafe-au-lait spots\n- Sleep onset insomnia\n- Delayed ability to walk\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Ambiguous genitalia\n- Choanal stenosis\n- Single transverse palmar crease\n- Prominent fingertip pads\n- Seizure\n- Generalized hypotonia\n- Cerebellar vermis hypoplasia\n- Absent speech\n- Anteriorly placed anus\n- Abnormal heart morphology\n- Coarctation of aorta\n- Overlapping toe\n- Dysphagia\n- Gastroesophageal reflux\n- Obstructive sleep apnea\n- Inverted nipples\n- Hypoplastic left heart\n- Sagittal craniosynostosis\n- Bilateral sensorineural hearing impairment\n- Infantile muscular hypotonia\n- Central sleep apnea\n- Intellectual disability, severe\n- EEG with abnormally slow frequencies\n- Hypoplastic aortic arch\n- Tube feeding\n- Cerebral visual impairment\n- Epileptic encephalopathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Epicanthus\n- Hypertelorism\n- Cupped ear\n- Preauricular skin tag\n- Conductive hearing impairment\n- Sensorineural hearing impairment\n- Nasolacrimal duct obstruction\n- Upslanted palpebral fissure\n- Depression\n- Compulsive behaviors\n- Anxiety\n- Delayed speech and language development\n- Specific learning disability\n- Ventricular septal defect\n- Subvalvular aortic stenosis\n- Gastroesophageal reflux\n- Decreased body weight\n- Poor appetite\n- Microtia\n- Vascular ring\n- Feeding difficulties\n- Abnormal subclavian artery morphology\n- Crohn's disease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Chronic otitis media\n- Macrotia\n- Hypermetropia\n- Dental crowding\n- Autistic behavior\n- Delayed speech and language development\n- Failure to thrive\n- Phimosis\n- Constipation\n- Intellectual disability, moderate\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Chronic otitis media\n- Macrotia\n- Hypermetropia\n- Dental crowding\n- Autistic behavior\n- Delayed speech and language development\n- Failure to thrive\n- Phimosis\n- Constipation\n- Intellectual disability, moderate\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Prominent fingertip pads\n- Seizure\n- Generalized hypotonia\n- Small for gestational age\n- Overlapping toe\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- High, narrow palate\n- Obstructive sleep apnea\n- Inverted nipples\n- Decreased body weight\n- Infantile muscular hypotonia\n- Aplasia of the falx cerebri\n- Multifocal epileptiform discharges\n- Intellectual disability, severe\n- Perisylvian polymicrogyria\n- Moderate hearing impairment\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Prominent fingertip pads\n- Seizure\n- Generalized hypotonia\n- Small for gestational age\n- Overlapping toe\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- High, narrow palate\n- Obstructive sleep apnea\n- Inverted nipples\n- Decreased body weight\n- Infantile muscular hypotonia\n- Aplasia of the falx cerebri\n- Multifocal epileptiform discharges\n- Intellectual disability, severe\n- Perisylvian polymicrogyria\n- Moderate hearing impairment\n- Cerebral visual impairment\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/02557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Microcephaly\n- Epicanthus\n- Mandibular prognathia\n- Overfolded helix\n- Anteverted nares\n- Hyperopic astigmatism\n- Deeply set eye\n- Upslanted palpebral fissure\n- Anxiety\n- Low frustration tolerance\n- Delayed speech and language development\n- Single transverse palmar crease\n- Prominent fingertip pads\n- Ataxia\n- Hypotonia\n- Intrauterine growth retardation\n- Constipation\n- Intellectual disability, moderate\n- Sleep disturbance\n- Almond-shaped palpebral fissure\n- Osteochondritis dissecans\n- Moderate global developmental delay\n- Endometriosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Protruding ear\n- Deeply set eye\n- Blue sclerae\n- Osteopenia\n- Osteoporosis\n- Arachnodactyly\n- Intellectual disability, mild\n- Joint hypermobility\n- Failure to thrive\n- Disproportionate tall stature\n- Constipation\n- Abnormality of speech or vocalization\n- Kyphosis\n- Shortened PR interval\n- Prominent forehead\n- Mild global developmental delay\n- Feeding difficulties\n- Metatarsal fracture\n- Arachnoid cyst\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Failure to thrive\n- Intrauterine growth retardation\n- Deep philtrum\n- Short stature\n- Decreased body weight\n- Narrow philtrum\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Coarse facial features\n- Wide nasal bridge\n- Autism\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Intellectual disability, mild\n- Large for gestational age\n- Talipes equinovarus\n- Loss of speech\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Attention deficit hyperactivity disorder\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Orofacial cleft\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Low-set ears\n- Astigmatism\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Intellectual disability, mild\n- Small for gestational age\n- Hypernasal speech\n- Atrial septal defect\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Birth length less than 3rd percentile\n- Short stature\n- Decreased body weight\n- Infantile muscular hypotonia\n- Short finger\n- Abnormality of the palmar creases\n- Midface retrusion\n- Unilateral conductive hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Conductive hearing impairment\n- Anteverted nares\n- Deeply set eye\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Hypothyroidism\n- Broad palm\n- Tapered finger\n- Prominent fingertip pads\n- Global developmental delay\n- Intrauterine growth retardation\n- Atrial septal defect\n- Pulmonic stenosis\n- Broad foot\n- Highly arched eyebrow\n- Short stature\n- Decreased body weight\n- Focal polymicrogyria\n- Tube feeding\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Recurrent otitis media\n- Prominent nasal bridge\n- Deeply set eye\n- Amblyopia\n- Congenital hypothyroidism\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Enlarged cisterna magna\n- Intellectual disability, moderate\n- Poor speech\n- Bilateral sensorineural hearing impairment\n- Feeding difficulties\n- Abnormal hippocampus morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Hypotelorism\n- Atypical behavior\n- Hypertrichosis\n- Obesity\n- Broad foot\n- Intellectual disability, moderate\n- Genu valgum\n- Feeding difficulties in infancy\n- Abnormal nasal base norphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Broad nasal tip\n- Long eyelashes\n- Delayed speech and language development\n- Axillary freckling\n- Multiple lentigines\n- Intellectual disability, mild\n- Dysarthria\n- Small for gestational age\n- Pes planus\n- Hypoplastic toenails\n- Intellectual disability, moderate\n- Recurrent infections\n- Increased body weight\n- Low hanging columella\n- Diminished ability to concentrate\n- Sparse eyebrow\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Ventricular septal defect\n- Pulmonic stenosis\n- Bilateral cleft lip and palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Urinary incontinence\n- Thin upper lip vermilion\n- Furrowed tongue\n- Long philtrum\n- Micrognathia\n- Recurrent otitis media\n- Astigmatism\n- Long palpebral fissure\n- Ectropion\n- Oligodontia\n- Atypical behavior\n- Delayed speech and language development\n- Single transverse palmar crease\n- Prominent fingertip pads\n- Hypotonia\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Constipation\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Sleep disturbance\n- Excessive wrinkled skin\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydrocele testis\n- Renal duplication\n- Narrow mouth\n- Cleft palate\n- Pierre-Robin sequence\n- Overfolded helix\n- Aggressive behavior\n- Autistic behavior\n- Patent foramen ovale\n- Lower limb spasticity\n- Sleep disturbance\n- Recurrent infections\n- 2-3 toe syndactyly\n- Periventricular leukomalacia\n- Bilateral conductive hearing impairment\n- Moderate global developmental delay\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Anteverted nares\n- Deeply set eye\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Autistic behavior\n- Hypothyroidism\n- Broad palm\n- Tapered finger\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Short toe\n- Broad toe\n- Highly arched eyebrow\n- Short nose\n- Short palm\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/02570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Low-set ears\n- Aggressive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Motor delay\n- Downturned corners of mouth\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Obesity\n- Downturned corners of mouth\n- Spindle-shaped finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Obesity\n- Downturned corners of mouth\n- Narrow palpebral fissure\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Posteriorly rotated ears\n- Underdeveloped nasal alae\n- Intellectual disability, mild\n- Exaggerated cupid's bow\n- Microtia\n- Feeding difficulties in infancy\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Posteriorly rotated ears\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Joint hypermobility\n- Intention tremor\n- Exaggerated cupid's bow\n- Depressed nasal bridge\n- Attention deficit hyperactivity disorder\n- Microtia\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Synophrys\n- Autism\n- Seizure\n- Intellectual disability, mild\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Short stature\n- Attention deficit hyperactivity disorder\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Epicanthus\n- Prominent nasal bridge\n- Hypotelorism\n- Autistic behavior\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Ventriculomegaly\n- Short palm\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/02577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Abnormality of the philtrum\n- Hypertelorism\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Overfolded helix\n- Autistic behavior\n- Delayed speech and language development\n- Hypertension\n- Prominent fingertip pads\n- Ataxia\n- Global developmental delay\n- Cerebellar atrophy\n- Hypertonia\n- Generalized non-motor (absence) seizure\n- Intellectual disability, moderate\n- Abnormal cerebral white matter morphology\n- Short distal phalanx of the 3rd finger\n- Prominent nasal tip\n- Microtia\n- Short distal phalanx of the 4th finger\n- Short distal phalanx of the 2nd finger\n- Abnormal columella morphology\n- Multifocal atrial tachycardia\n- Short palpebral fissure\n- Overweight\n- Clinodactyly\n- Hippocampal atrophy\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Facial asymmetry\n- Prominent antihelix\n- Bulbous nose\n- Hypermetropia\n- Autistic behavior\n- Delayed speech and language development\n- Cafe-au-lait spot\n- Cyanosis\n- Motor delay\n- Hip dysplasia\n- Joint laxity\n- Growth delay\n- Intellectual disability, moderate\n- Genu recurvatum\n- Clinodactyly of the 5th finger\n- Narrow philtrum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Tall stature\n- Dolichocephaly\n- Malar flattening\n- Retrognathia\n- Mandibular prognathia\n- Wide nose\n- Thick eyebrow\n- Depression\n- Autistic behavior\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Slender finger\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Disproportionate tall stature\n- Decreased fetal movement\n- Pes planus\n- Poor suck\n- Sleep disturbance\n- High, narrow palate\n- Poor appetite\n- Attention deficit hyperactivity disorder\n- Atypical absence seizure\n- Equinus calcaneus\n- Long toe\n- Broad uvula\n- Slender toe\n- Auditory sensitivity\n- Frequent temper tantrums\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Autistic behavior\n- Delayed speech and language development\n- Jaundice\n- Intellectual disability, mild\n- Motor delay\n- Poor suck\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Attention deficit hyperactivity disorder\n- Large earlobe\n- Uplifted earlobe\n- Moderate global developmental delay\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Depression\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Global developmental delay\n- Specific learning disability\n- Thick nasal alae\n- Shyness\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Delayed speech and language development\n- Eczema\n- Motor delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Hypoglycemia\n- Profound global developmental delay\n- Decreased serum zinc\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Anteverted nares\n- Intellectual disability, mild\n- Motor delay\n- Deep philtrum\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Expressive language delay\n- Prominent nasal tip\n- Thick nasal alae\n- Delayed fine motor development\n- Simple ear\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nose\n- Intellectual disability, mild\n- Finger syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Epicanthus inversus\n- Compulsive behaviors\n- Delayed speech and language development\n- Motor delay\n- Intellectual disability, moderate\n- Sparse lateral eyebrow\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/02599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/02600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Dolichocephaly\n- Micrognathia\n- Protruding ear\n- Delayed speech and language development\n- Intrauterine growth retardation\n- Ventriculomegaly\n- Recurrent lower respiratory tract infections\n- Short stature\n- Decreased body weight\n- Intracranial cystic lesion\n- Scaphocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/02601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Dolichocephaly\n- Hypertrichosis\n- Intrauterine growth retardation\n- Recurrent lower respiratory tract infections\n- Short stature\n- Decreased body weight\n- Simplified gyral pattern\n- Moderate global developmental delay\n- Scaphocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/02602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Dolichocephaly\n- Micrognathia\n- Intrauterine growth retardation\n- Asthma\n- Short stature\n- Decreased body weight\n- Simplified gyral pattern\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/02603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormal cochlea morphology\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Specific learning disability\n- Absent speech\n- Rectal prolapse\n- Ventriculomegaly\n- Cavum septum pellucidum\n- Intussusception\n- Hernia of the abdominal wall\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Strabismus\n- Hypermetropia\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Syncope\n- Specific learning disability\n- Absent speech\n- Abnormal cerebral white matter morphology\n- Focal-onset seizure\n- Gastrostomy tube feeding in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Nystagmus\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Specific learning disability\n- Cerebral hypomyelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Astigmatism\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Absent speech\n- Ventriculomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Myopia\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Specific learning disability\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n- Cerebellar vermis atrophy\n- Speech apraxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Autism\n- Delayed speech and language development\n- Motor delay\n- Specific learning disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/02610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Choanal stenosis\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Delayed speech and language development\n- Motor delay\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Preauricular skin tag\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Choanal stenosis\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Delayed speech and language development\n- Motor delay\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Delayed speech and language development\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Preauricular skin tag\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Delayed speech and language development\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Lacrimal duct atresia\n- Abnormality of the thyroid gland\n- Failure to thrive\n- Abnormal heart morphology\n- Asymmetric, linear skin defects\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/02615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Myopia\n- Nystagmus\n- Delayed eruption of teeth\n- Seizure\n- Agenesis of corpus callosum\n- Cardiomyopathy\n- Ventriculomegaly\n- Short stature\n- Decreased body weight\n- Severe muscular hypotonia\n- Hyperpigmented streaks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/02617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Delayed speech and language development\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Choanal stenosis\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Delayed speech and language development\n- Motor delay\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Microcephaly\n- Triangular face\n- Narrow forehead\n- Small forehead\n- Nystagmus\n- Synophrys\n- Dental malocclusion\n- Hypertrichosis\n- Intellectual disability\n- Spasticity\n- Global developmental delay\n- Vomiting\n- Prominent glabella\n- EEG abnormality\n- Hyperkinetic movements\n- High, narrow palate\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Temporal cortical atrophy\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Triangular face\n- Narrow forehead\n- Small forehead\n- Synophrys\n- Dental malocclusion\n- Hypertrichosis\n- Intellectual disability\n- Spasticity\n- Global developmental delay\n- Vomiting\n- Prominent glabella\n- Hyperkinetic movements\n- High, narrow palate\n- Short stature\n- Decreased body weight\n- Frontotemporal cerebral atrophy\n- Decreased head circumference\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Preauricular skin tag\n- Protruding ear\n- Prominent nasal bridge\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Preauricular skin tag\n- Protruding ear\n- Prominent nasal bridge\n- Bilateral choanal atresia\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Orofacial cleft\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Preauricular skin tag\n- Protruding ear\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Upslanted palpebral fissure\n- Lower eyelid coloboma\n- Bilateral cleft lip and palate\n- Short palpebral fissure\n- Narrow palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin vermilion border\n- Microcephaly\n- Downslanted palpebral fissures\n- Exotropia\n- Global developmental delay\n- Motor delay\n- Hypertonia\n- Absent speech\n- Brisk reflexes\n- Skeletal muscle atrophy\n- CNS hypomyelination\n- Short stature\n- Decreased body weight\n- Cachexia\n- Prominent eyelashes\n- Gastrostomy tube feeding in infancy\n- Type I diabetes mellitus\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Low-set ears\n- Bulbous nose\n- Hypertrichosis\n- Arachnodactyly\n- Intellectual disability\n- Seizure\n- Spasticity\n- Global developmental delay\n- Vomiting\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Cerebral dysmyelination\n- Brain atrophy\n- Decreased head circumference\n- Enlarged sylvian cistern\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Low-set ears\n- Bulbous nose\n- Nystagmus\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Bilateral multifocal epileptiform discharges\n- Increased urine glutamate level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Narrow forehead\n- Low-set ears\n- Bulbous nose\n- Pectus carinatum\n- Intellectual disability\n- Seizure\n- Ataxia\n- Spasticity\n- Global developmental delay\n- Cerebral atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Bilateral multifocal epileptiform discharges\n- Thick vermilion border\n- Decreased head circumference\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Low-set ears\n- Bulbous nose\n- Hypertrichosis\n- Arachnodactyly\n- Intellectual disability\n- Ataxia\n- Spasticity\n- Global developmental delay\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Frontotemporal cerebral atrophy\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Low-set ears\n- Bulbous nose\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Rigidity\n- Gait ataxia\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Thick vermilion border\n- Increased urine glutamate level\n- Decreased head circumference\n- EEG with temporal epileptiform discharges\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Low-set ears\n- Bulbous nose\n- Intellectual disability\n- Global developmental delay\n- Cerebellar atrophy\n- Cerebral cortical atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Low voltage EEG\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocele testis\n- Microcephaly\n- Triangular face\n- Narrow forehead\n- Low-set ears\n- Bulbous nose\n- Hypertrichosis\n- Intellectual disability\n- Global developmental delay\n- Hyperkinetic movements\n- Abnormal cerebral white matter morphology\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Brain atrophy\n- Thick vermilion border\n- Retractile testis\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow forehead\n- Low-set ears\n- Bulbous nose\n- Nystagmus\n- Arachnodactyly\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Rigidity\n- Cerebral cortical atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Multifocal epileptiform discharges\n- Brain atrophy\n- Thick vermilion border\n- Decreased head circumference\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/02637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Hypotonia\n- Frontal bossing\n- Delayed gross motor development\n- Depressed nasal bridge\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/02638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Hypotonia\n- Frontal bossing\n- Delayed gross motor development\n- Depressed nasal bridge\n- Multifocal cerebral white matter abnormalities\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/02639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Frontal bossing\n- Delayed gross motor development\n- Abnormal periventricular white matter morphology\n- Depressed nasal bridge\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/02640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Delayed speech and language development\n- Frontal bossing\n- Depressed nasal bridge\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/02641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Frontal bossing\n- Abnormal periventricular white matter morphology\n- Depressed nasal bridge\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/02642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bipolar affective disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Pointed chin\n- Posteriorly rotated ears\n- Prominent nasal bridge\n- Broad nasal tip\n- Telecanthus\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Telecanthus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/02669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Everted lower lip vermilion\n- Long face\n- Triangular face\n- Anteverted nares\n- Downslanted palpebral fissures\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Everted lower lip vermilion\n- Long face\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Optic disc pallor\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Ventriculomegaly\n- EEG abnormality\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the corpus callosum\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Strabismus\n- Optic disc pallor\n- Nystagmus\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Hypoplasia of the corpus callosum\n- Depressed nasal bridge\n- Prominent forehead\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Mandibular prognathia\n- Long philtrum\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Blue sclerae\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Short nose\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Blue sclerae\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Mandibular prognathia\n- Anteverted nares\n- Blue sclerae\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Deeply set eye\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Global developmental delay\n- Short nose\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Intellectual disability\n- Global developmental delay\n- Short nose\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Long philtrum\n- Anteverted nares\n- Deeply set eye\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Short nose\n- Depressed nasal bridge\n- Sparse hair\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Everted lower lip vermilion\n- Strabismus\n- Deeply set eye\n- Optic disc pallor\n- Atypical behavior\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Myopia\n- Blue sclerae\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Chiari malformation\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Triangular face\n- Deeply set eye\n- Blue sclerae\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Cortical dysplasia\n- Accelerated skeletal maturation\n- Periventricular leukomalacia\n- Aplasia\/Hypoplasia of the optic nerve\n- Periventricular nodular heterotopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Hypermetropia\n- Blue sclerae\n- Atypical behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Hypoplasia of the corpus callosum\n- Kyphoscoliosis\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Blue sclerae\n- Atypical behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Exaggerated cupid's bow\n- EEG abnormality\n- Short nose\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- EEG abnormality\n- Kyphoscoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Myopia\n- Atypical behavior\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Short nose\n- Accelerated skeletal maturation\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Atypical behavior\n- Pectus excavatum\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Optic disc pallor\n- Myopia\n- Blue sclerae\n- Nystagmus\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- EEG abnormality\n- Kyphoscoliosis\n- Short nose\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Triangular face\n- Deeply set eye\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Kyphoscoliosis\n- Short nose\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Anteverted nares\n- Downslanted palpebral fissures\n- Myopia\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Exaggerated cupid's bow\n- EEG abnormality\n- Kyphoscoliosis\n- Short nose\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Astigmatism\n- Downslanted palpebral fissures\n- Atypical behavior\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Short nose\n- Accelerated skeletal maturation\n- Joint contracture of the hand\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Atypical behavior\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Orthostatic hypotension\n- Joint laxity\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Short nose\n- Decreased body weight\n- Accelerated skeletal maturation\n- Peripheral visual field loss\n- Sparse hair\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Prominent forehead\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Atypical behavior\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Chiari malformation\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Deeply set eye\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Ventriculomegaly\n- Short nose\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Optic disc pallor\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- EEG abnormality\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Atypical behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Atypical behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Triangular face\n- Long philtrum\n- Strabismus\n- Deeply set eye\n- Atypical behavior\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Hypermetropia\n- Optic disc pallor\n- Myopia\n- Nystagmus\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Migraine\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Facial asymmetry\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- EEG abnormality\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Myopia\n- Atypical behavior\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Bulbous nose\n- Prominent nasal bridge\n- Strabismus\n- Brachydactyly\n- Hypotonia\n- Absent speech\n- Laryngomalacia\n- Atrial septal defect\n- Gastroesophageal reflux\n- Bronchomalacia\n- Chronic lung disease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Abnormality of the dentition\n- Cleft palate\n- Prominent nasal bridge\n- Strabismus\n- Absent speech\n- Ventricular septal defect\n- Gastroesophageal reflux\n- Intestinal malrotation\n- Chronic lung disease\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Preauricular skin tag\n- Macrotia\n- Broad nasal tip\n- Strabismus\n- Ptosis\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Craniosynostosis\n- Atrial septal defect\n- Patent ductus arteriosus\n- Downturned corners of mouth\n- Periventricular leukomalacia\n- Tented upper lip vermilion\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Macrotia\n- Broad nasal tip\n- Strabismus\n- Ptosis\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Craniosynostosis\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Cavum septum pellucidum\n- Downturned corners of mouth\n- Sagittal craniosynostosis\n- Tented upper lip vermilion\n- Metopic synostosis\n- Feeding difficulties\n- EEG with generalized spikes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Narrow mouth\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Conical tooth\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Hepatomegaly\n- Downturned corners of mouth\n- Preauricular pit\n- Wide intermamillary distance\n- Lacrimal duct stenosis\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow forehead\n- Broad nasal tip\n- Short attention span\n- Delayed speech and language development\n- Single transverse palmar crease\n- Global developmental delay\n- Neonatal hypotonia\n- Atrial septal defect\n- Patent ductus arteriosus\n- Sydney crease\n- Cerebral visual impairment\n- Abnormal cardiac catheterization\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Triangular mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Impaired social interactions\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Neonatal hypotonia\n- Plagiocephaly\n- Neonatal respiratory distress\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Abnormal visual fixation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Narrow forehead\n- Posteriorly rotated ears\n- Broad nasal tip\n- Strabismus\n- Hypermetropia\n- Delayed speech and language development\n- Global developmental delay\n- Abnormality of dental morphology\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/02711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Abnormality of the dentition\n- Triangular mouth\n- Gingival overgrowth\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- High forehead\n- Hearing impairment\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Long eyelashes\n- Blue sclerae\n- Brachydactyly\n- Umbilical hernia\n- Frontal bossing\n- Mesomelia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Broad hallux\n- Bifid tongue\n- Broad thumb\n- Midface retrusion\n- Clinodactyly\n- Increased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/02712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Abnormality of the kidney\n- Abnormality of the dentition\n- Triangular mouth\n- Gingival overgrowth\n- Macrocephaly\n- Wide anterior fontanel\n- Hypertelorism\n- High forehead\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Abnormal sternum morphology\n- Brachydactyly\n- Omphalocele\n- Frontal bossing\n- Mesomelia\n- Short nose\n- Depressed nasal bridge\n- Short phalanx of finger\n- Duplication of the distal phalanx of hand\n- Broad hallux\n- Broad thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/02713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Abnormality of the dentition\n- Triangular mouth\n- Gingival overgrowth\n- Macrocephaly\n- Wide anterior fontanel\n- Hypertelorism\n- High forehead\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Anteverted nares\n- Proptosis\n- Abnormal sternum morphology\n- Brachydactyly\n- Frontal bossing\n- Mesomelia\n- Short nose\n- Depressed nasal bridge\n- Short phalanx of finger\n- Duplication of the distal phalanx of hand\n- Broad hallux\n- Broad thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/02714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cryptorchidism\n- Hypospadias\n- Hypospadias\n- Micropenis\n- Micropenis\n- Abnormality of the dentition\n- Abnormality of the dentition\n- Triangular mouth\n- Triangular mouth\n- Gingival overgrowth\n- Gingival overgrowth\n- Macrocephaly\n- Macrocephaly\n- Epicanthus\n- Epicanthus\n- Hypertelorism\n- Hypertelorism\n- Long philtrum\n- Long philtrum\n- High forehead\n- High forehead\n- Wide nasal bridge\n- Wide nasal bridge\n- Abnormal sternum morphology\n- Abnormal sternum morphology\n- Seizure\n- Seizure\n- Umbilical hernia\n- Umbilical hernia\n- Frontal bossing\n- Frontal bossing\n- Scoliosis\n- Scoliosis\n- Mesomelia\n- Mesomelia\n- Short nose\n- Short nose\n- Depressed nasal bridge\n- Depressed nasal bridge\n- Broad hallux\n- Broad hallux\n- Absent uvula\n- Absent uvula\n- Bifid tongue\n- Bifid tongue\n- Increased bone mineral density\n- Increased bone mineral density\n- Midface retrusion\n- Midface retrusion\n- Abnormal renal morphology\n- Abnormal renal morphology\n- Camptodactyly\n- Camptodactyly\n- Clinodactyly\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/02715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Brachycephaly\n- Long philtrum\n- High forehead\n- Hearing impairment\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Visual impairment\n- Cataract\n- Upslanted palpebral fissure\n- Intellectual disability, mild\n- Pericardial effusion\n- Sparse scalp hair\n- EEG abnormality\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Dislocated radial head\n- Short nose\n- Craniofacial asymmetry\n- Depressed nasal bridge\n- Nail dystrophy\n- Enlarged semicircular canal\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Malar flattening\n- Long philtrum\n- Sensorineural hearing impairment\n- Broad neck\n- Downslanted palpebral fissures\n- Visual impairment\n- Ptosis\n- Cataract\n- Autistic behavior\n- Hypothyroidism\n- Brachydactyly\n- Intellectual disability\n- Limitation of joint mobility\n- Constipation\n- Bilateral tonic-clonic seizure\n- Low posterior hairline\n- Short nose\n- Clinodactyly of the 5th finger\n- Broad eyebrow\n- Midface retrusion\n- Testicular torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Brachycephaly\n- Malar flattening\n- Epicanthus\n- High forehead\n- Low-set ears\n- Stenosis of the external auditory canal\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Cataract\n- Upslanted palpebral fissure\n- Intellectual disability, mild\n- Atrial septal defect\n- Pericarditis\n- Ventriculomegaly\n- EEG abnormality\n- Short nose\n- Craniofacial asymmetry\n- Depressed nasal bridge\n- Macular hypopigmentation\n- Cone dystrophy\n- Midface retrusion\n- Abnormal frontal bone morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Malar flattening\n- Epicanthus\n- Mandibular prognathia\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Visual impairment\n- Ptosis\n- Cataract\n- Thickened skin\n- Cerebral atrophy\n- Ventriculomegaly\n- Sparse scalp hair\n- EEG abnormality\n- Large sella turcica\n- Short nose\n- Clinodactyly of the 5th finger\n- Craniofacial asymmetry\n- Depressed nasal bridge\n- Chiari type I malformation\n- Nail dystrophy\n- Intellectual disability, severe\n- Broad eyebrow\n- Abnormality of joint mobility\n- Midface retrusion\n- Albuminuria\n- Agenesis of canine\n- Febrile seizure outside the age of 3 months to 6 years\n- Camptodactyly of finger\n- Breast aplasia\n- Abnormal frontal bone morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Delayed cranial suture closure\n- Malar flattening\n- Mandibular prognathia\n- Hypertelorism\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Ptosis\n- Cataract\n- Pectus carinatum\n- Intellectual disability\n- Pericarditis\n- Hiatus hernia\n- Bilateral tonic-clonic seizure\n- Radioulnar synostosis\n- Short nose\n- Chiari type I malformation\n- Macular hypopigmentation\n- Broad eyebrow\n- Abnormality of joint mobility\n- Midface retrusion\n- Central diaphragmatic hernia\n- Febrile seizure outside the age of 3 months to 6 years\n- Breast aplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cataract\n- Osteopenia\n- Thin skin\n- Cutis laxa\n- Adducted thumb\n- Hypotonia\n- Brisk reflexes\n- Joint laxity\n- Delayed closure of the anterior fontanelle\n- Intrauterine growth retardation\n- Talipes equinovarus\n- Wormian bones\n- Small foramen magnum\n- Hip dislocation\n- Excessive wrinkled skin\n- Postnatal growth retardation\n- Dermal translucency\n- Abnormality of the curvature of the vertebral column\n- Feeding difficulties\n- obsolete Psychomotor retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/02721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Cataract\n- Thin skin\n- Cutis laxa\n- Hypotonia\n- Joint laxity\n- Intrauterine growth retardation\n- Vascular tortuosity\n- Os odontoideum\n- Excessive wrinkled skin\n- Postnatal growth retardation\n- Dermal translucency\n- Feeding difficulties\n- obsolete Psychomotor retardation\n- Hernia\n- Dysharmonic bone age\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/02722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Cataract\n- Osteopenia\n- Thin skin\n- Cutis laxa\n- Adducted thumb\n- Hypotonia\n- Brisk reflexes\n- Joint laxity\n- Delayed closure of the anterior fontanelle\n- Intrauterine growth retardation\n- Talipes equinovarus\n- Hip dislocation\n- Excessive wrinkled skin\n- Postnatal growth retardation\n- Dermal translucency\n- Abnormality of the curvature of the vertebral column\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/02723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Cleft palate\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Delayed speech and language development\n- Craniosynostosis\n- Hip dysplasia\n- Atrial septal defect\n- Talipes equinovarus\n- Constipation\n- Gastroesophageal reflux\n- Hypoplasia of the corpus callosum\n- Scoliosis\n- Downturned corners of mouth\n- Inverted nipples\n- Prominent metopic ridge\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ptosis\n- Proptosis\n- Shallow orbits\n- Craniosynostosis\n- Hip dysplasia\n- Constipation\n- Chronic diarrhea\n- Gastrointestinal dysmotility\n- Scoliosis\n- Downturned corners of mouth\n- Inverted nipples\n- Preauricular pit\n- Prominent metopic ridge\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydronephrosis\n- Furrowed tongue\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ptosis\n- Delayed speech and language development\n- Constipation\n- Gastroesophageal reflux\n- Scoliosis\n- Coxa valga\n- Inverted nipples\n- Syringomyelia\n- Preauricular pit\n- Abnormal vertebral segmentation and fusion\n- Anterior open-bite malocclusion\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydronephrosis\n- Furrowed tongue\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ptosis\n- Delayed speech and language development\n- Constipation\n- Gastroesophageal reflux\n- Scoliosis\n- Coxa valga\n- Inverted nipples\n- Syringomyelia\n- Preauricular pit\n- Abnormal vertebral segmentation and fusion\n- Anterior open-bite malocclusion\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Vesicoureteral reflux\n- Sensorineural hearing impairment\n- Proptosis\n- Shallow orbits\n- Plagiocephaly\n- Hip dysplasia\n- Ventricular septal defect\n- Pulmonic stenosis\n- Talipes\n- Gastroesophageal reflux\n- Hypoplasia of the corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Cleft palate\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ventricular septal defect\n- Hypoplasia of the corpus callosum\n- Difficulty walking\n- Downturned corners of mouth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Cleft palate\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ventricular septal defect\n- Hypoplasia of the corpus callosum\n- Difficulty walking\n- Downturned corners of mouth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Cleft palate\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ventricular septal defect\n- Hypoplasia of the corpus callosum\n- Difficulty walking\n- Downturned corners of mouth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/02731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Open mouth\n- Narrow forehead\n- Low-set ears\n- Bulbous nose\n- Strabismus\n- Long eyelashes\n- Epicanthus inversus\n- Hypermetropia\n- Autism\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Cerebral atrophy\n- Abnormality of the palmar creases\n- Protruding tongue\n- Prominent forehead\n- Sydney crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Open mouth\n- Narrow forehead\n- Low-set ears\n- Bulbous nose\n- Strabismus\n- Long eyelashes\n- Epicanthus inversus\n- Hypermetropia\n- Autism\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Cerebral atrophy\n- Abnormality of the palmar creases\n- Protruding tongue\n- Prominent forehead\n- Sydney crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Open mouth\n- Brachycephaly\n- Malar flattening\n- Full cheeks\n- Low-set ears\n- Bulbous nose\n- Wide nasal bridge\n- Short neck\n- Hypermetropia\n- Esotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Patent foramen ovale\n- Highly arched eyebrow\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Retrognathia\n- Macrotia\n- Bulbous nose\n- Wide nasal bridge\n- Prominent nose\n- Strabismus\n- Downslanted palpebral fissures\n- Hypermetropia\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Overlapping toe\n- Duane anomaly\n- Speech apraxia\n- Delayed myelination\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Open mouth\n- Brachycephaly\n- Low-set ears\n- Stenosis of the external auditory canal\n- Bulbous nose\n- Autism\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Metatarsus adductus\n- Depressed nasal bridge\n- Protruding tongue\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Open mouth\n- Brachycephaly\n- Low-set ears\n- Stenosis of the external auditory canal\n- Bulbous nose\n- Autism\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Metatarsus adductus\n- Depressed nasal bridge\n- Protruding tongue\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Hydroureter\n- Wide mouth\n- Macroglossia\n- Open mouth\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Bulbous nose\n- Hypermetropia\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Tetralogy of Fallot\n- Short foot\n- Metatarsus adductus\n- Overlapping toe\n- Short nose\n- Hip contracture\n- Focal white matter lesions\n- Contracture of thumb\n- Feeding difficulties\n- Necrotizing enterocolitis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Hydroureter\n- Wide mouth\n- Macroglossia\n- Open mouth\n- Broad forehead\n- Narrow forehead\n- High forehead\n- Low-set ears\n- Bulbous nose\n- Hypermetropia\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Tetralogy of Fallot\n- Short foot\n- Metatarsus adductus\n- Overlapping toe\n- Short nose\n- Hip contracture\n- Focal white matter lesions\n- Contracture of thumb\n- Feeding difficulties\n- Necrotizing enterocolitis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Open mouth\n- Long eyelashes\n- Delayed speech and language development\n- Global developmental delay\n- Agenesis of corpus callosum\n- Dystonia\n- Frontal bossing\n- Spastic paraparesis\n- Depressed nasal bridge\n- Severe muscular hypotonia\n- Bilateral microphthalmos\n- Corneal opacity\n- Ectopia pupillae\n- Protruding tongue\n- Horizontal eyebrow\n- Broad eyebrow\n- Anterior synechiae of the anterior chamber\n- Short palpebral fissure\n- Oral motor hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/02740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Low-set ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Depressed nasal tip\n- Short neck\n- Developmental cataract\n- Abnormality of the incisor\n- Microdontia\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability, mild\n- Limitation of joint mobility\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Kyphosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Knee flexion contracture\n- Microtia\n- Midface retrusion\n- Feeding difficulties\n- Camptodactyly\n- Limited ankle dorsiflexion\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Low-set ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Depressed nasal tip\n- Short neck\n- Developmental cataract\n- Abnormality of the incisor\n- Microdontia\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability, mild\n- Limitation of joint mobility\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Kyphosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Knee flexion contracture\n- Microtia\n- Midface retrusion\n- Feeding difficulties\n- Camptodactyly\n- Limited ankle dorsiflexion\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Low-set ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Depressed nasal tip\n- Short neck\n- Developmental cataract\n- Abnormality of the incisor\n- Microdontia\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability, mild\n- Limitation of joint mobility\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Kyphosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Knee flexion contracture\n- Microtia\n- Midface retrusion\n- Feeding difficulties\n- Camptodactyly\n- Limited ankle dorsiflexion\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Telecanthus\n- Retinal hemorrhage\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Plagiocephaly\n- Limitation of joint mobility\n- Patent ductus arteriosus\n- Pericarditis\n- Neonatal hypoglycemia\n- Radioulnar synostosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Broad eyebrow\n- Midface retrusion\n- Abnormal optic disc morphology\n- Sparse eyebrow\n- Fetal pericardial effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Telecanthus\n- Retinal hemorrhage\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Plagiocephaly\n- Limitation of joint mobility\n- Patent ductus arteriosus\n- Pericarditis\n- Neonatal hypoglycemia\n- Radioulnar synostosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Broad eyebrow\n- Midface retrusion\n- Abnormal optic disc morphology\n- Sparse eyebrow\n- Fetal pericardial effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Telecanthus\n- Retinal hemorrhage\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Plagiocephaly\n- Limitation of joint mobility\n- Patent ductus arteriosus\n- Pericarditis\n- Neonatal hypoglycemia\n- Radioulnar synostosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Broad eyebrow\n- Midface retrusion\n- Abnormal optic disc morphology\n- Sparse eyebrow\n- Fetal pericardial effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Telecanthus\n- Retinal hemorrhage\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Plagiocephaly\n- Limitation of joint mobility\n- Patent ductus arteriosus\n- Pericarditis\n- Neonatal hypoglycemia\n- Radioulnar synostosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Broad eyebrow\n- Midface retrusion\n- Abnormal optic disc morphology\n- Sparse eyebrow\n- Fetal pericardial effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Telecanthus\n- Retinal hemorrhage\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Plagiocephaly\n- Limitation of joint mobility\n- Patent ductus arteriosus\n- Pericarditis\n- Neonatal hypoglycemia\n- Radioulnar synostosis\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Broad eyebrow\n- Midface retrusion\n- Abnormal optic disc morphology\n- Sparse eyebrow\n- Fetal pericardial effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Macroglossia\n- Narrow mouth\n- Thin upper lip vermilion\n- Hydrocephalus\n- Large fontanelles\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Downslanted palpebral fissures\n- Telecanthus\n- Developmental cataract\n- Microphthalmia\n- Autism\n- Delayed speech and language development\n- Pectus excavatum\n- Hypothyroidism\n- Precocious puberty\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Limitation of joint mobility\n- Neonatal hypoglycemia\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Depressed nasal bridge\n- Fixed elbow flexion\n- Chiari type I malformation\n- Broad eyebrow\n- Midface retrusion\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Abnormal pinna morphology\n- Sensorineural hearing impairment\n- Telecanthus\n- Delayed speech and language development\n- Juvenile cataract\n- Seizure\n- Motor delay\n- Neonatal hypotonia\n- Limitation of joint mobility\n- Overlapping toe\n- Limited elbow flexion\/extension\n- Chiari type I malformation\n- Feeding difficulties in infancy\n- High myopia\n- Broad eyebrow\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Abnormal pinna morphology\n- Sensorineural hearing impairment\n- Telecanthus\n- Delayed speech and language development\n- Juvenile cataract\n- Seizure\n- Motor delay\n- Neonatal hypotonia\n- Limitation of joint mobility\n- Overlapping toe\n- Limited elbow flexion\/extension\n- Chiari type I malformation\n- Feeding difficulties in infancy\n- High myopia\n- Broad eyebrow\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Abnormal pinna morphology\n- Sensorineural hearing impairment\n- Telecanthus\n- Delayed speech and language development\n- Juvenile cataract\n- Seizure\n- Motor delay\n- Neonatal hypotonia\n- Limitation of joint mobility\n- Overlapping toe\n- Limited elbow flexion\/extension\n- Chiari type I malformation\n- Feeding difficulties in infancy\n- High myopia\n- Broad eyebrow\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/02752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Aggressive behavior\n- Autistic behavior\n- Intellectual disability, mild\n- Motor delay\n- Intellectual disability, moderate\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/02753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Aggressive behavior\n- Intellectual disability, moderate\n- Short stature\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/02754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Inability to walk\n- Short stature\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/02755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mitral regurgitation\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Tricuspid regurgitation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Atrial septal defect\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability, mild\n- Hemihypertrophy\n- Umbilical hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Atrial septal defect\n- Intellectual disability, moderate\n- Sagittal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability, moderate\n- Scoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Intellectual disability, moderate\n- Patellar subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/02763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Scoliosis\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Scoliosis\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Cerebellar atrophy\n- Scoliosis\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Delayed speech and language development\n- Albinism\n- Seizure\n- Hypotonia\n- Motor delay\n- Apnea\n- Lateral ventricle dilatation\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Delayed speech and language development\n- Albinism\n- Seizure\n- Hypotonia\n- Motor delay\n- Apnea\n- Lateral ventricle dilatation\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Aggressive behavior\n- Autism with high cognitive abilities\n- Sacral dimple\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Pes planus\n- Constipation\n- Abnormality of coordination\n- Feeding difficulties\n- Dorsal hirsutism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Aggressive behavior\n- Autism with high cognitive abilities\n- Sacral dimple\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Pes planus\n- Constipation\n- Abnormality of coordination\n- Feeding difficulties\n- Dorsal hirsutism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Delayed speech and language development\n- Pectus excavatum\n- Sacral dimple\n- Motor delay\n- Neonatal hypotonia\n- Intellectual disability, moderate\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hyperactivity\n- Global developmental delay\n- Motor delay\n- Sleep disturbance\n- Oromotor apraxia\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Aggressive behavior\n- Compulsive behaviors\n- Attention deficit hyperactivity disorder\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Aggressive behavior\n- Compulsive behaviors\n- Attention deficit hyperactivity disorder\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Intellectual disability, mild\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Intellectual disability, mild\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Motor delay\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Motor delay\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Joint laxity\n- Asthma\n- Headache\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Chiari type I malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypermetropia\n- Carious teeth\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypermetropia\n- Carious teeth\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Scoliosis\n- Burkitt lymphoma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/02782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Joint dislocation\n- Talipes equinovarus\n- Vertebral fusion\n- Tapered humerus\n- Short stature\n- Pseudoepiphyses of the metacarpals\n- Broad distal phalanx of finger\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/02783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/02784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Small face\n- Micrognathia\n- Sensorineural hearing impairment\n- Anteverted nares\n- Retinal detachment\n- Myopia\n- Short nose\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/02785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Delayed speech and language development\n- Broad palm\n- Global developmental delay\n- Motor delay\n- Coxa valga\n- Delayed skeletal maturation\n- Dislocated radial head\n- Elevated circulating alkaline phosphatase concentration\n- Postnatal growth retardation\n- Aplasia\/Hypoplasia of the distal phalanx of the 5th finger\n- Intellectual disability, severe\n- Prominent forehead\n- Broad thumb\n- Thick vermilion border\n- Clinodactyly\n- Long thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Delayed speech and language development\n- Broad palm\n- Global developmental delay\n- Motor delay\n- Coxa valga\n- Delayed skeletal maturation\n- Dislocated radial head\n- Elevated circulating alkaline phosphatase concentration\n- Postnatal growth retardation\n- Aplasia\/Hypoplasia of the distal phalanx of the 5th finger\n- Intellectual disability, severe\n- Prominent forehead\n- Broad thumb\n- Thick vermilion border\n- Clinodactyly\n- Long thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Short philtrum\n- Long palpebral fissure\n- Diastema\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Pachygyria\n- Plagiocephaly\n- Anteriorly placed anus\n- Small nail\n- Bilateral tonic-clonic seizure\n- Cerebral cortical atrophy\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Short distal phalanx of the 5th finger\n- Hyperconvex thumb nails\n- Short distal phalanx of the 2nd finger\n- Short distal phalanx of the thumb\n- Short distal phalanx of hallux\n- Midface retrusion\n- Aspiration pneumonia\n- Feeding difficulties\n- Delayed myelination\n- Tube feeding\n- Short distal phalanx of the 4th toe\n- Short distal phalanx of the 5th toe\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Long palpebral fissure\n- Talipes equinovalgus\n- Hip dislocation\n- Cervical kyphosis\n- Elbow flexion contracture\n- Knee dislocation\n- Depressed nasal bridge\n- Spinal dysraphism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/02789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin vermilion border\n- Triangular face\n- Low-set ears\n- Cupped ear\n- Narrow nasal ridge\n- Thin skin\n- Cutis laxa\n- Intellectual disability\n- Global developmental delay\n- Joint hypermobility\n- Hip dysplasia\n- Intrauterine growth retardation\n- Pes planus\n- Delayed gross motor development\n- Excessive wrinkled skin\n- Adipose tissue loss\n- Sunken cheeks\n- Dermal translucency\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/02790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydroureter\n- Hydronephrosis\n- Coarse facial features\n- Mandibular prognathia\n- Hypertelorism\n- Short philtrum\n- Upslanted palpebral fissure\n- Diastema\n- Acne\n- Single umbilical artery\n- Seizure\n- Hypotonia\n- Growth delay\n- Oligohydramnios\n- Anonychia\n- Short distal phalanx of toe\n- Elevated circulating alkaline phosphatase concentration\n- Shortening of all distal phalanges of the fingers\n- Short distal phalanx of finger\n- Tented upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Motor delay\n- Generalized non-motor (absence) seizure\n- Skeletal muscle atrophy\n- Short stature\n- Severe muscular hypotonia\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long face\n- Mandibular prognathia\n- Narrow nose\n- Adducted thumb\n- Intellectual disability\n- Global developmental delay\n- Joint hypermobility\n- Intrauterine growth retardation\n- Pes planus\n- Decreased body weight\n- Deep palmar crease\n- Excessive wrinkled skin\n- Prominent veins on trunk\n- Prematurely aged appearance\n- Palmoplantar cutis laxa\n- Lipodystrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/02793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long face\n- Mandibular prognathia\n- Narrow nose\n- Adducted thumb\n- Intellectual disability\n- Global developmental delay\n- Joint hypermobility\n- Intrauterine growth retardation\n- Pes planus\n- Decreased body weight\n- Deep palmar crease\n- Excessive wrinkled skin\n- Prominent veins on trunk\n- Prematurely aged appearance\n- Palmoplantar cutis laxa\n- Lipodystrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/02794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Cleft soft palate\n- Thin upper lip vermilion\n- Low-set ears\n- Broad nasal tip\n- Tapered finger\n- Seizure\n- Dandy-Walker malformation\n- Bilateral ptosis\n- Pes planus\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Widely-spaced incisors\n- Generalized neonatal hypotonia\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Aggressive behavior\n- Delayed speech and language development\n- Hyperactivity\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/02796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Retrognathia\n- Epicanthus\n- Smooth philtrum\n- Long philtrum\n- Low-set ears\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Microdontia\n- Atypical behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Weak cry\n- Exaggerated cupid's bow\n- Elevated circulating alkaline phosphatase concentration\n- Decreased body weight\n- Prominent nasal tip\n- Large earlobe\n- Self-biting\n- Narrow palpebral fissure\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the genitourinary system\n- Wide mouth\n- Cleft palate\n- Coarse facial features\n- Full cheeks\n- Microretrognathia\n- Hypertelorism\n- Facial asymmetry\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Telecanthus\n- Upslanted palpebral fissure\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Abnormal heart morphology\n- Frontal bossing\n- Morphological central nervous system abnormality\n- Aganglionic megacolon\n- Elevated circulating alkaline phosphatase concentration\n- Aplasia\/Hypoplasia of the 5th finger\n- Tented upper lip vermilion\n- Feeding difficulties\n- Anorectal anomaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/02798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Ptosis\n- Syndactyly\n- Microtia\n- Prominent crus of helix\n- Round ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/02799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/02800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Recurrent otitis media\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Myopia\n- Delayed speech and language development\n- Specific learning disability\n- Polyhydramnios\n- Ventricular septal defect\n- Esophageal atresia\n- Postural instability\n- Tracheoesophageal fistula\n- Overriding aorta\n- Bilateral cleft lip and palate\n- Bronchomalacia\n- Spina bifida occulta\n- Short stature\n- Decreased body weight\n- Aplasia of the semicircular canal\n- Hypoplasia of the semicircular canal\n- Unilateral cryptorchidism\n- Esodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/02801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Hearing impairment\n- Abnormal pinna morphology\n- Retinal coloboma\n- Microphthalmia\n- Iris coloboma\n- Depression\n- Intrauterine growth retardation\n- Abnormality of the nail\n- Medulloblastoma\n- Preauricular pit\n- Sparse hair\n- Cleft of chin\n- Abnormal renal morphology\n- Bilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/02802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Cleft soft palate\n- High palate\n- Microcephaly\n- Epicanthus\n- Micrognathia\n- Macrotia\n- Anteverted nares\n- Hypotonia\n- Agenesis of corpus callosum\n- Growth delay\n- Pyloric stenosis\n- 2-3 toe syndactyly\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/02803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microretrognathia\n- Hypertelorism\n- Low-set ears\n- Myopia\n- Dental malocclusion\n- Delayed eruption of permanent teeth\n- Hypopigmentation of the skin\n- Seizure\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Hypoplastic male external genitalia\n- Cleft palate\n- Microcephaly\n- Epicanthus\n- Narrow forehead\n- Micrognathia\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Ptosis\n- Aggressive behavior\n- Irritability\n- Anxiety\n- Vitiligo\n- Intellectual disability\n- Hypocholesterolemia\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Short thumb\n- Elevated 7-dehydrocholesterol\n- Gastrostomy tube feeding in infancy\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/02805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Delayed cranial suture closure\n- Dental malocclusion\n- Brachydactyly\n- Joint laxity\n- Wormian bones\n- Hypoplastic iliac wing\n- Depressed nasal bridge\n- Multiple unerupted teeth\n- Failure of eruption of permanent teeth\n- Aplasia\/Hypoplasia of the clavicles\n- Delayed pubic bone ossification\n- Supernumerary tooth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/02806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Limitation of joint mobility\n- Failure to thrive\n- Episodic vomiting\n- Recurrent upper respiratory tract infections\n- Lumbar scoliosis\n- Decreased finger mobility\n- Limited wrist movement\n- Limited elbow flexion\n- Airway obstruction\n- Decreased distal sensory nerve action potential\n- Increased bone mineral density\n- Constrictive median neuropathy\n- Allergy\n- Lower limb pain\n- Shoulder pain\n- Ectrodactyly\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/02807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Limitation of joint mobility\n- Failure to thrive\n- Episodic vomiting\n- Recurrent upper respiratory tract infections\n- Lumbar scoliosis\n- Decreased finger mobility\n- Limited wrist movement\n- Limited elbow flexion\n- Airway obstruction\n- Decreased distal sensory nerve action potential\n- Increased bone mineral density\n- Constrictive median neuropathy\n- Allergy\n- Lower limb pain\n- Shoulder pain\n- Ectrodactyly\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/02808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Microcephaly\n- Retrognathia\n- Hypertelorism\n- Wide nasal bridge\n- Convex nasal ridge\n- Strabismus\n- Glaucoma\n- Long eyelashes\n- Dental crowding\n- Hypertension\n- Hirsutism\n- Nevus flammeus\n- Intellectual disability\n- Global developmental delay\n- Constipation\n- Highly arched eyebrow\n- Recurrent infections\n- Prominent nasal septum\n- Type II diabetes mellitus\n- Neoplasm of the skin\n- Broad hallux\n- Keloids\n- Prominent forehead\n- Broad thumb\n- Cutaneous horn\n- Irregular dentition\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Wide nasal bridge\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Developmental cataract\n- Long eyelashes\n- Nasolacrimal duct obstruction\n- Dental crowding\n- Hypertrichosis\n- Delayed ossification of carpal bones\n- Failure to thrive\n- Growth delay\n- Bilateral talipes equinovarus\n- Hallux valgus\n- Dysphagia\n- Facial hypertrichosis\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Short distal phalanx of the 3rd finger\n- Clinodactyly of the 5th finger\n- Prominent nasal septum\n- Short distal phalanx of the 4th finger\n- Short distal phalanx of the 2nd finger\n- Broad distal phalanx of finger\n- Broad hallux\n- Short hallux\n- Macroscopic hematuria\n- Pilomatrixoma\n- Decreased prealbumin level\n- Decreased serum zinc\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Bifid uvula\n- Thin upper lip vermilion\n- Full cheeks\n- Smooth philtrum\n- High forehead\n- Conductive hearing impairment\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Choanal atresia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Oligodontia\n- Delayed speech and language development\n- Prominent fingertip pads\n- Specific learning disability\n- Joint hypermobility\n- Gastroesophageal reflux\n- Clinodactyly of the 5th finger\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/02811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Gingival overgrowth\n- Coarse facial features\n- Epicanthus\n- Low anterior hairline\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Abnormality of the periorbital region\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Eczema\n- Motor delay\n- Hyperconvex nail\n- Generalized-onset seizure\n- Intellectual disability, moderate\n- Thoracic scoliosis\n- Prominent interphalangeal joints\n- Sparse hair\n- Broad eyebrow\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/02812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Gingival overgrowth\n- Coarse facial features\n- Epicanthus\n- Low anterior hairline\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Abnormality of the periorbital region\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Eczema\n- Motor delay\n- Hyperconvex nail\n- Generalized-onset seizure\n- Intellectual disability, moderate\n- Thoracic scoliosis\n- Prominent interphalangeal joints\n- Sparse hair\n- Broad eyebrow\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/02813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Hypertelorism\n- Smooth philtrum\n- Long philtrum\n- Thickened helices\n- Macrotia\n- Deeply set eye\n- Downslanted palpebral fissures\n- Hypotonia\n- Recurrent respiratory infections\n- Short nose\n- Premature anterior fontanel closure\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/02814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Round face\n- Posteriorly rotated ears\n- Convex nasal ridge\n- Prominent nose\n- Exotropia\n- Bilateral ptosis\n- Broad finger\n- Obesity\n- Short toe\n- Broad toe\n- Shortening of all distal phalanges of the fingers\n- Hallux varus\n- Short finger\n- Low hanging columella\n- Broad hallux\n- Broad thumb\n- Clubbing of toes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Sloping forehead\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Widely spaced teeth\n- Growth delay\n- Oligohydramnios\n- Ventricular septal defect\n- Pneumonia\n- Pulmonary arterial hypertension\n- Rhabdomyosarcoma\n- Long nose\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- 2-3 toe syndactyly\n- Mild global developmental delay\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/02818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Depressed nasal tip\n- Strabismus\n- Deeply set eye\n- Posterior embryotoxon\n- Jaundice\n- Optic nerve dysplasia\n- Tetralogy of Fallot\n- Butterfly vertebrae\n- Coronal craniosynostosis\n- Abnormal finger flexion crease\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/02819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Delayed speech and language development\n- Large hands\n- Hypotonia\n- Large for gestational age\n- Long foot\n- Hypoglycemia\n- Frontal bossing\n- Delayed gross motor development\n- Birth length greater than 97th percentile\n- Feeding difficulties\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Delayed speech and language development\n- Large hands\n- Hypotonia\n- Large for gestational age\n- Long foot\n- Hypoglycemia\n- Frontal bossing\n- Delayed gross motor development\n- Birth length greater than 97th percentile\n- Feeding difficulties\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Posteriorly rotated ears\n- Bulbous nose\n- Abnormal nasal bridge morphology\n- Telecanthus\n- Epicanthus inversus\n- Blue irides\n- Syndactyly\n- Wrist flexion contracture\n- Abnormal nasal morphology\n- Decreased palmar creases\n- Depigmentation\/hyperpigmentation of skin\n- Ulnar deviation of finger\n- Narrow naris\n- White hair\n- Flexion contracture of finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/02823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Posteriorly rotated ears\n- Bulbous nose\n- Abnormal nasal bridge morphology\n- Telecanthus\n- Epicanthus inversus\n- Blue irides\n- Syndactyly\n- Wrist flexion contracture\n- Abnormal nasal morphology\n- Decreased palmar creases\n- Depigmentation\/hyperpigmentation of skin\n- Ulnar deviation of finger\n- Narrow naris\n- White hair\n- Flexion contracture of finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/02824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Posteriorly rotated ears\n- Bulbous nose\n- Abnormal nasal bridge morphology\n- Telecanthus\n- Epicanthus inversus\n- Blue irides\n- Syndactyly\n- Wrist flexion contracture\n- Abnormal nasal morphology\n- Decreased palmar creases\n- Depigmentation\/hyperpigmentation of skin\n- Ulnar deviation of finger\n- Narrow naris\n- White hair\n- Flexion contracture of finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/02825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Hypertelorism\n- Protruding ear\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Downslanted palpebral fissures\n- Narrow nasal tip\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/02826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Global developmental delay\n- Increased body weight\n- Accelerated skeletal maturation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydroureter\n- Pointed chin\n- Wide nasal bridge\n- Deeply set eye\n- Abnormally large globe\n- Hypotonia\n- Global developmental delay\n- Deep philtrum\n- Hypoplasia of the corpus callosum\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Recurrent upper respiratory tract infections\n- Feeding difficulties in infancy\n- Uplifted earlobe\n- Medial flaring of the eyebrow\n- Dilatation of the renal pelvis\n- Colpocephaly\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Micrognathia\n- Abnormality of the auditory canal\n- Abnormal pinna morphology\n- Downslanted palpebral fissures\n- Lacrimal duct atresia\n- Sparse eyelashes\n- Abnormal zygomatic arch morphology\n- Mild conductive hearing impairment\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Hydrocephalus\n- Malar flattening\n- Micrognathia\n- Abnormality of the outer ear\n- Atresia of the external auditory canal\n- Choanal atresia\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Gastroesophageal reflux\n- Multiple suture craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micrognathia\n- Narrow nasal ridge\n- Proptosis\n- Absent eyelashes\n- Dental crowding\n- Abnormality of skin pigmentation\n- Arthritis\n- Joint stiffness\n- Alopecia\n- Absent eyebrow\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- Persistent open anterior fontanelle\n- Aplastic clavicle\n- Generalized lipodystrophy\n- Osteolytic defects of the phalanges of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Failure to thrive\n- Panhypogammaglobulinemia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/02832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Broad face\n- Epicanthus\n- Square face\n- Strabismus\n- Myopia\n- Synophrys\n- Atypical behavior\n- Restlessness\n- Self-mutilation\n- Hyperactivity\n- Single transverse palmar crease\n- Brachydactyly\n- Broad palm\n- Global developmental delay\n- Motor delay\n- Hoarse voice\n- Sleep disturbance\n- Short palm\n- Tented upper lip vermilion\n- Midface retrusion\n- Head-banging\n- Polyembolokoilamania\n- Onychotillomania\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/02833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Large fontanelles\n- Microcephaly\n- Micrognathia\n- Narrow nose\n- Delayed eruption of teeth\n- Narrow chest\n- Dry skin\n- Thin skin\n- Failure to thrive\n- Alopecia\n- Short nail\n- Sparse scalp hair\n- Wormian bones\n- Coxa valga\n- Ovoid vertebral bodies\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- Shortening of all distal phalanges of the toes\n- Shortening of all distal phalanges of the fingers\n- Nail dystrophy\n- Osteolytic defects of the distal phalanges of the hand\n- Abnormality of the temporomandibular joint\n- Temporal bossing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Broad face\n- Prominent supraorbital ridges\n- Macrotia\n- Broad neck\n- Deeply set eye\n- Delayed speech and language development\n- Increased body weight\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/02836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/02837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Intellectual disability\n- Short stature\n- Broad hallux\n- Keloids\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Brachycephaly\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Sloping forehead\n- Narrow forehead\n- Wide nasal bridge\n- Prominent nose\n- Astigmatism\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Global developmental delay\n- Hepatic steatosis\n- Small for gestational age\n- Endocardial fibroelastosis\n- Neutropenia\n- Asthma\n- Hepatomegaly\n- Lymphadenopathy\n- Long nose\n- Clinodactyly of the 5th finger\n- T-cell acute lymphoblastic leukemias\n- Ecchymosis\n- Diffuse alveolar damage\n- Pulmonary hemorrhage\n- Mediastinal mass\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/02839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Mandibular prognathia\n- Deeply set eye\n- Delayed speech and language development\n- Global developmental delay\n- Agenesis of corpus callosum\n- Fine hair\n- Sparse hair\n- Uplifted earlobe\n- Exodeviation\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Telecanthus\n- Hypopigmentation of the skin\n- Heterochromia iridis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/02841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the outer ear\n- Hearing impairment\n- Abnormal cochlea morphology\n- Choanal stenosis\n- Iris coloboma\n- Facial palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/02842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Broad nasal tip\n- Bifid nasal tip\n- Strabismus\n- Split nail\n- Bilateral cleft lip and palate\n- Craniofacial asymmetry\n- Clinodactyly\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Epicanthus\n- Facial hypotonia\n- Pointed chin\n- Hypertelorism\n- Low-set ears\n- Delayed speech and language development\n- Clinodactyly of the 5th finger\n- Large earlobe\n- Uplifted earlobe\n- Medial flaring of the eyebrow\n- Broad eyebrow\n- Distal joint laxity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Hypertelorism\n- Wide nasal bridge\n- Wide nose\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Delayed speech and language development\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Large for gestational age\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Generalized-onset seizure\n- Bilateral cleft lip and palate\n- Recurrent upper respiratory tract infections\n- Decreased body weight\n- Prominent nasal tip\n- Depressed nasal bridge\n- Shortening of all distal phalanges of the fingers\n- Uplifted earlobe\n- Broad hallux\n- Broad thumb\n- Severe global developmental delay\n- Severe conductive hearing impairment\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Full cheeks\n- Convex nasal ridge\n- Narrow nasal bridge\n- Proptosis\n- Sparse eyelashes\n- Dental crowding\n- Prominent superficial veins\n- Failure to thrive\n- Alopecia\n- Frontal bossing\n- Wormian bones\n- Enlarged joints\n- Short stature\n- Decreased body weight\n- Sparse hair\n- Lipodystrophy\n- Osteolytic defects of the distal phalanges of the hand\n- Short distal phalanx of finger\n- Prominent forehead\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocele testis\n- Broad face\n- Delayed speech and language development\n- Enuresis\n- Brachydactyly\n- Specific learning disability\n- Asthma\n- Sleep disturbance\n- Decreased body weight\n- Attention deficit hyperactivity disorder\n- Few cafe-au-lait spots\n- Midface retrusion\n- Skin-picking\n- Fetal distress\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/02847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Coarse facial features\n- Epicanthus\n- Full cheeks\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Telecanthus\n- Hyperkeratosis\n- Seizure\n- Limitation of joint mobility\n- Barrel-shaped chest\n- Redundant skin\n- Hoarse voice\n- Ventricular septal defect\n- Mitral valve prolapse\n- Hypertrophic cardiomyopathy\n- Thin nail\n- Deep plantar creases\n- Hypoglycemia\n- Respiratory distress\n- Curly hair\n- Fine hair\n- Chiari malformation\n- Hypocalcemia\n- Short stature\n- Decreased body weight\n- Prominent nasal tip\n- Depressed nasal bridge\n- Postnatal macrocephaly\n- Deep palmar crease\n- Sparse hair\n- Nail dystrophy\n- Ulnar deviation of finger\n- Large earlobe\n- Broad distal phalanx of finger\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/02848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypertelorism\n- Facial asymmetry\n- Broad nasal tip\n- Strabismus\n- Esotropia\n- Pectus carinatum\n- Frontal bossing\n- Coronal craniosynostosis\n- Ridged fingernail\n- Broad hallux\n- Abnormality of the palmar creases\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Sparse eyelashes\n- Prominent scalp veins\n- Flexion contracture\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Short stature\n- Decreased body weight\n- Persistent open anterior fontanelle\n- Osteolytic defects of the phalanges of the hand\n- Sparse eyebrow\n- Scleroderma\n- Chin with vertical crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Sparse eyelashes\n- Prominent scalp veins\n- Flexion contracture\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Short stature\n- Decreased body weight\n- Persistent open anterior fontanelle\n- Osteolytic defects of the phalanges of the hand\n- Sparse eyebrow\n- Scleroderma\n- Chin with vertical crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Sparse eyelashes\n- Prominent scalp veins\n- Flexion contracture\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Short stature\n- Decreased body weight\n- Persistent open anterior fontanelle\n- Osteolytic defects of the phalanges of the hand\n- Sparse eyebrow\n- Scleroderma\n- Chin with vertical crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Trismus\n- Micrognathia\n- Narrow nose\n- Ectropion\n- Thin skin\n- Tapered finger\n- Intrauterine growth retardation\n- Vomiting\n- Poor suck\n- Hepatomegaly\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Multiple joint contractures\n- Short nose\n- Generalized bone demineralization\n- Dermal translucency\n- Stiff skin\n- Keratosis pilaris\n- Cleft hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Trismus\n- Micrognathia\n- Narrow nose\n- Ectropion\n- Thin skin\n- Tapered finger\n- Intrauterine growth retardation\n- Vomiting\n- Poor suck\n- Hepatomegaly\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Multiple joint contractures\n- Short nose\n- Generalized bone demineralization\n- Dermal translucency\n- Stiff skin\n- Keratosis pilaris\n- Cleft hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Hypoplasia of the maxilla\n- Broad forehead\n- Wide nose\n- Proptosis\n- Short clavicles\n- Pes planus\n- Frontal bossing\n- Coxa vara\n- Short nose\n- Short stature\n- Widely patent fontanelles and sutures\n- Depressed nasal bridge\n- Delayed pubic bone ossification\n- Short distal phalanx of finger\n- Wide cranial sutures\n- Supernumerary tooth\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/02855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Hypoplasia of the maxilla\n- Broad forehead\n- Wide nose\n- Proptosis\n- Short clavicles\n- Pes planus\n- Frontal bossing\n- Coxa vara\n- Short nose\n- Short stature\n- Widely patent fontanelles and sutures\n- Depressed nasal bridge\n- Delayed pubic bone ossification\n- Short distal phalanx of finger\n- Wide cranial sutures\n- Supernumerary tooth\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/02856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Joint stiffness\n- Hepatosplenomegaly\n- Short stature\n- Decreased body weight\n- Abnormal metacarpal morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/02857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Shawl scrotum\n- Pectus excavatum\n- Specific learning disability\n- Bilateral talipes equinovarus\n- Sandal gap\n- Bilateral tonic-clonic seizure\n- Clinodactyly of the 5th finger\n- Pes valgus\n- Bilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/02858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Hypoplasia of the semicircular canal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/02859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Prominent occiput\n- Epicanthus\n- High forehead\n- Macrotia\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Strabismus\n- Proptosis\n- Dental crowding\n- Intellectual disability\n- Bilateral ptosis\n- Failure to thrive\n- Redundant skin\n- Metatarsus adductus\n- Short nose\n- Prominent metopic ridge\n- Alveolar ridge overgrowth\n- Feeding difficulties\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/02860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Dolichocephaly\n- Low-set, posteriorly rotated ears\n- Incomplete partition of the cochlea type II\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Supernumerary nipple\n- Bilateral sensorineural hearing impairment\n- Enlarged vestibular aqueduct\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/02861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Recurrent otitis media\n- Prominent nasal bridge\n- Pancytopenia\n- Recurrent upper respiratory tract infections\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/02862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Full cheeks\n- Micrognathia\n- Convex nasal ridge\n- Short clavicles\n- Hyperpigmentation of the skin\n- Thin skin\n- Pruritus\n- Joint hypermobility\n- Alopecia\n- Short nail\n- Diarrhea\n- Constipation\n- Scoliosis\n- Delayed skeletal maturation\n- Severe short stature\n- Broad phalanx\n- Nail dystrophy\n- Short distal phalanx of finger\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Coarse facial features\n- Mandibular prognathia\n- Pointed chin\n- Triangular face\n- Large hands\n- Long foot\n- Asthma\n- Poor coordination\n- Expressive language delay\n- Sparse hair\n- Type I diabetes mellitus\n- Lipedema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retinal coloboma\n- Microphthalmia\n- Iris coloboma\n- Growth delay\n- Omphalocele\n- Dermal atrophy\n- Focal dermal aplasia\/hypoplasia\n- Underdeveloped supraorbital ridges\n- Papilloma\n- Ectrodactyly\n- Lower limb asymmetry\n- Toenail dysplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/02865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Severe short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/02866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/02867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/02868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/02869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/02870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/02871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/02872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/02875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/02876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/02877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/02878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/02879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/02880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Maxillozygomatic hypoplasia\n- Microtia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Triangular face\n- Posteriorly rotated ears\n- Preauricular skin tag\n- Downslanted palpebral fissures\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Short attention span\n- Hypertrichosis\n- Seizure\n- Sandal gap\n- Constipation\n- Low posterior hairline\n- Sparse scalp hair\n- High, narrow palate\n- Enlarged joints\n- Mild short stature\n- Feeding difficulties in infancy\n- Long toe\n- Severe global developmental delay\n- Dry hair\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/02882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Triangular face\n- Posteriorly rotated ears\n- Preauricular skin tag\n- Downslanted palpebral fissures\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Short attention span\n- Hypertrichosis\n- Seizure\n- Sandal gap\n- Constipation\n- Low posterior hairline\n- Sparse scalp hair\n- High, narrow palate\n- Enlarged joints\n- Mild short stature\n- Feeding difficulties in infancy\n- Long toe\n- Severe global developmental delay\n- Dry hair\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/02883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/02885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/02886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/02887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/02888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/02889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/02890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/02891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/02894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/02897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/02899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/02904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Bicornuate uterus\n- Umbilical hernia\n- Bilateral cleft lip and palate\n- Prominent forehead\n- Bilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/02906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/02907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/02909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/02911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/02913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Triangular face\n- Anteverted nares\n- Proptosis\n- Blue sclerae\n- Hypoplasia of teeth\n- Frontal bossing\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Triangular face\n- Anteverted nares\n- Proptosis\n- Blue sclerae\n- Hypoplasia of teeth\n- Frontal bossing\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/02917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/02921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/02922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/02923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/02924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/02925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/02929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/02933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/02934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/02937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/02938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/02939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/02940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/02941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Exotropia\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Prominent fingertip pads\n- Motor delay\n- Abnormal corpus callosum morphology\n- Constipation\n- Broad-based gait\n- Poor motor coordination\n- Poor speech\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Mild microcephaly\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/02942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Exotropia\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Prominent fingertip pads\n- Motor delay\n- Abnormal corpus callosum morphology\n- Constipation\n- Broad-based gait\n- Poor motor coordination\n- Poor speech\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Mild microcephaly\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/02943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/02944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/02945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/02946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypertelorism\n- Facial hemangioma\n- Hearing impairment\n- Low-set ears\n- Thickened helices\n- Short neck\n- Intellectual disability\n- Cerebellar atrophy\n- Generalized hypotonia\n- Absent speech\n- Failure to thrive\n- Growth delay\n- Atrial septal defect\n- Pulmonic stenosis\n- Short foot\n- Constipation\n- Gastroesophageal reflux\n- Delayed gross motor development\n- Difficulty walking\n- Downturned corners of mouth\n- Tracheomalacia\n- Respiratory failure\n- Short palm\n- Short stature\n- Feeding difficulties\n- Capillary malformation\n- Tube feeding\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Abnormality of the forehead\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Pectus carinatum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hyperreflexia\n- Polyhydramnios\n- Downturned corners of mouth\n- Hypoplastic helices\n- Feeding difficulties\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Abnormality of the forehead\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Pectus carinatum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hyperreflexia\n- Downturned corners of mouth\n- Hypoplastic helices\n- Feeding difficulties\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Telecanthus\n- Single transverse palmar crease\n- Large hands\n- Global developmental delay\n- Hypertonia\n- Absent speech\n- Brisk reflexes\n- Pes planus\n- Long foot\n- Vomiting\n- Gait ataxia\n- Downturned corners of mouth\n- Limited knee extension\n- Short nose\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Mild myopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Abnormal pinna morphology\n- Telecanthus\n- Intellectual disability\n- Global developmental delay\n- Gait disturbance\n- Neonatal hypotonia\n- Cardiomyopathy\n- Vomiting\n- Constipation\n- Feeding difficulties in infancy\n- Long toe\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Brachycephaly\n- Macrocephaly\n- Epicanthus\n- Smooth philtrum\n- Abnormal pinna morphology\n- Downslanted palpebral fissures\n- Telecanthus\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Constipation\n- Gastroesophageal reflux\n- Progressive spasticity\n- Lower limb hyperreflexia\n- Inability to walk\n- Feeding difficulties\n- Delayed ability to walk\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Cryptorchidism\n- Macrocephaly\n- Anxiety\n- Abnormality of the skeletal system\n- Dry skin\n- Numerous nevi\n- Polyhydramnios\n- Tetralogy of Fallot\n- Constipation\n- Poor suck\n- Choroid plexus cyst\n- Delayed gross motor development\n- Short stature\n- Decreased body weight\n- Dysplastic distal radial epiphyses\n- Wide intermamillary distance\n- Fetal pyelectasis\n- Feeding difficulties\n- Stooped posture\n- Low APGAR score\n- Keratosis pilaris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Epicanthus\n- Hypertelorism\n- High forehead\n- Abnormal pinna morphology\n- Anteverted nares\n- Hypotonia\n- Motor delay\n- Hepatosplenomegaly\n- Respiratory distress\n- Postural instability\n- Ventricular septal hypertrophy\n- Spinal muscular atrophy\n- Hyperintensity of cerebral white matter on MRI\n- Neonatal sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/02958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/02970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/02980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/02981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/02982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/02983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/02984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/02999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/03009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/03030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/03049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/03050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/03068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/03081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Absent eyelashes\n- Osteopenia\n- Osteoporosis\n- Abnormal metaphysis morphology\n- Poikiloderma\n- Intellectual disability, mild\n- Small for gestational age\n- Chronic diarrhea\n- Patchy alopecia\n- Delayed skeletal maturation\n- Patellar hypoplasia\n- Short nose\n- Short stature\n- 2-3 toe syndactyly\n- Sparse hair\n- Mixed hypo- and hyperpigmentation of the skin\n- Concave nasal ridge\n- Feeding difficulties\n- Hodgkin lymphoma\n- Osteoma cutis\n- Calcinosis cutis\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Hypermetropia\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Scanning speech\n- Short palm\n- Supernumerary maxillary incisor\n- Short finger\n- Cleft maxillary alveolar ridge\n- Mild microcephaly\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/03083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Periorbital fullness\n- Short attention span\n- Delayed speech and language development\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Joint hypermobility\n- Recurrent respiratory infections\n- Clinodactyly of the 5th finger\n- Decreased facial expression\n- Abnormal social behavior\n- Insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/03084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Cleft soft palate\n- Thin upper lip vermilion\n- Low anterior hairline\n- Narrow forehead\n- Underdeveloped nasal alae\n- Anteverted nares\n- Deeply set eye\n- Autistic behavior\n- Ventricular septal defect\n- Atrial septal defect\n- Coarctation of aorta\n- Sandal gap\n- Large forehead\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- 2-3 toe syndactyly\n- Tented upper lip vermilion\n- Laterally extended eyebrow\n- Broad thumb\n- Feeding difficulties\n- Left ventricular outflow tract obstruction\n- Congenital lobar overinflation\n- Thin eyebrow\n- Cleft hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/03092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Smooth philtrum\n- Hearing impairment\n- Macrotia\n- Broad nasal tip\n- Microcornea\n- Widely spaced teeth\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Intrauterine growth retardation\n- Short toe\n- Intellectual disability, moderate\n- Scoliosis\n- Hip dislocation\n- Short stature\n- Abnormality of dental eruption\n- Short finger\n- High anterior hairline\n- Abnormality of the palmar creases\n- Abnormal plantar dermatoglyphics\n- Brain atrophy\n- Wide nasal ridge\n- Prominent subcalcaneal fat pad\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Malar flattening\n- Smooth philtrum\n- Macrotia\n- Broad nasal tip\n- Microcornea\n- Widely spaced teeth\n- Pectus excavatum\n- Prominent fingertip pads\n- Hypotonia\n- Neonatal hypotonia\n- Short toe\n- Deep plantar creases\n- Talipes\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Relative macrocephaly\n- Deep palmar crease\n- Short finger\n- High anterior hairline\n- Intellectual disability, severe\n- Broad thumb\n- Severe global developmental delay\n- Brain atrophy\n- Wide nasal ridge\n- Prominent subcalcaneal fat pad\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/03114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/03127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Trigonocephaly\n- Long face\n- Retrognathia\n- Epicanthus\n- Micrognathia\n- Strabismus\n- Hypermetropia\n- Emotional lability\n- Delayed speech and language development\n- Hyperactivity\n- Striae distensae\n- Tapered finger\n- Intellectual disability, mild\n- Joint hypermobility\n- Pes planus\n- Sandal gap\n- Recurrent infections\n- Cubitus valgus\n- Aortic aneurysm\n- Patellar subluxation\n- Metopic synostosis\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/03128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Autism\n- Anxiety\n- Delayed speech and language development\n- Hirsutism\n- Intellectual disability, mild\n- Sandal gap\n- Constipation\n- Frontal upsweep of hair\n- 2-3 toe syndactyly\n- Mild global developmental delay\n- Ingrown nail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/03129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Brachydactyly\n- Fine hair\n- Short stature\n- Sparse lateral eyebrow\n- Tapered phalanx of finger\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/03130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/03136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/03137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/03138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/03139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/03140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/03141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Macrotia\n- Sensorineural hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Ptosis\n- Long palpebral fissure\n- Synophrys\n- Cervical ribs\n- Short tubular bones of the hand\n- Seizure\n- Intellectual disability, mild\n- Global developmental delay\n- Low posterior hairline\n- Intellectual disability, moderate\n- Delayed skeletal maturation\n- Spina bifida occulta\n- Clinodactyly of the 5th finger\n- Short stature\n- Attention deficit hyperactivity disorder\n- Ulnar deviation of the 2nd finger\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/03142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Epispadias\n- Brachycephaly\n- Low anterior hairline\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Ptosis\n- Long palpebral fissure\n- Synophrys\n- Short tubular bones of the hand\n- Global developmental delay\n- Macrodontia\n- Low posterior hairline\n- Intellectual disability, moderate\n- Thoracic kyphosis\n- Spina bifida occulta\n- Abnormal vertebral morphology\n- Clinodactyly of the 5th finger\n- Short stature\n- Ulnar deviation of the 2nd finger\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/03143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Low anterior hairline\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Ptosis\n- Oligodontia\n- Anxiety\n- Hyperactivity\n- Cervical ribs\n- Short tubular bones of the hand\n- Macrodontia\n- Low posterior hairline\n- Intellectual disability, moderate\n- Abnormal vertebral morphology\n- Clinodactyly of the 5th finger\n- Short stature\n- Cutaneous finger syndactyly\n- Cutaneous syndactyly of toes\n- Diminished ability to concentrate\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/03144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/03145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/03146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/03149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/03150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/03151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/03152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/03153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/03154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Micrognathia\n- Atresia of the external auditory canal\n- Underdeveloped nasal alae\n- Retinal coloboma\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Iris coloboma\n- Seizure\n- Abnormal nasopharynx morphology\n- Respiratory distress\n- Microtia\n- Hypoplasia of the zygomatic bone\n- Unicoronal synostosis\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Transverse facial cleft\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Micrognathia\n- Atresia of the external auditory canal\n- Underdeveloped nasal alae\n- Retinal coloboma\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Iris coloboma\n- Seizure\n- Abnormal nasopharynx morphology\n- Respiratory distress\n- Microtia\n- Hypoplasia of the zygomatic bone\n- Unicoronal synostosis\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Transverse facial cleft\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Micrognathia\n- Atresia of the external auditory canal\n- Underdeveloped nasal alae\n- Retinal coloboma\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Iris coloboma\n- Seizure\n- Abnormal nasopharynx morphology\n- Respiratory distress\n- Microtia\n- Hypoplasia of the zygomatic bone\n- Unicoronal synostosis\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Transverse facial cleft\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/03160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/03161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/03162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/03163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/03164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/03165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Brachydactyly\n- Small nail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Kyphosis\n- Internally rotated shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Kyphosis\n- Internally rotated shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Kyphosis\n- Internally rotated shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Kyphosis\n- Internally rotated shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Autism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Cleft palate\n- Macrocephaly\n- Autism\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Autism\n- Intellectual disability\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Autism\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Autistic behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Intellectual disability\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Autism\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pachygyria\n- Thick corpus callosum\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pachygyria\n- Thick corpus callosum\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pachygyria\n- Thick corpus callosum\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pachygyria\n- Thick corpus callosum\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pachygyria\n- Thick corpus callosum\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Flexion contracture\n- Distal amyotrophy\n- Calcification of the auricular cartilage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/03198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Macrocephaly\n- Round face\n- Short philtrum\n- Hypothyroidism\n- Growth delay\n- Secundum atrial septal defect\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/03199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short philtrum\n- Wide nasal bridge\n- Myopia\n- Aggressive behavior\n- Low frustration tolerance\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/03200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Round face\n- Astigmatism\n- Hypermetropia\n- Amblyopia\n- Low frustration tolerance\n- Delayed speech and language development\n- Single transverse palmar crease\n- Hypertrichosis\n- Global developmental delay\n- Pes planus\n- Premature rupture of membranes\n- Constipation\n- Polyphagia\n- Pes valgus\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/03201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Round face\n- Short philtrum\n- Hypoplasia of the maxilla\n- Strabismus\n- Hypermetropia\n- Synophrys\n- Delayed speech and language development\n- Hypothyroidism\n- Hypertrichosis\n- Obesity\n- Pes planus\n- Short foot\n- Intermittent diarrhea\n- Genu valgum\n- Low hanging columella\n- Sleep apnea\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/03202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Aggressive behavior\n- Brachydactyly\n- Short foot\n- Short nail\n- Overlapping toe\n- Intellectual disability, moderate\n- Excessive salivation\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/03203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High forehead\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Neonatal hypotonia\n- Poor hand-eye coordination\n- Proximal placement of thumb\n- Flat face\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/03204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the philtrum\n- Delayed speech and language development\n- Hyperextensible skin\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Joint hypermobility\n- Polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the philtrum\n- Delayed speech and language development\n- Hyperextensible skin\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Joint hypermobility\n- Polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the philtrum\n- Hyperextensible skin\n- Neonatal hypotonia\n- Joint hypermobility\n- Thick corpus callosum\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the philtrum\n- Hyperextensible skin\n- Neonatal hypotonia\n- Joint hypermobility\n- Thick corpus callosum\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Aggressive behavior\n- Cutis marmorata\n- Nevus flammeus\n- Bicuspid aortic valve\n- Pulmonary embolism\n- 2-3 toe syndactyly\n- Ascending tubular aorta aneurysm\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Delayed speech and language development\n- Cutis marmorata\n- Hypotonia\n- Joint hypermobility\n- Hemihypertrophy\n- Scoliosis\n- Polydactyly\n- Intellectual disability, severe\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Nevus flammeus\n- Hemihypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/03211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic male external genitalia\n- Bifid uvula\n- Macrocephaly\n- Hypertelorism\n- Micrognathia\n- Downslanted palpebral fissures\n- Autism\n- Tapered finger\n- Seizure\n- Global developmental delay\n- Neonatal hypotonia\n- Cerebellar vermis hypoplasia\n- Failure to thrive\n- Global brain atrophy\n- Scoliosis\n- Tracheomalacia\n- Dysplastic corpus callosum\n- Sleep apnea\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Prominent nasal bridge\n- Downslanted palpebral fissures\n- Telecanthus\n- Aggressive behavior\n- Single transverse palmar crease\n- Hirsutism\n- Global developmental delay\n- Atrial septal defect\n- Scoliosis\n- Tracheomalacia\n- obsolete Prominent epicanthal folds\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/03213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ventricular septal defect\n- Atrial septal defect\n- Hypertrophic cardiomyopathy\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ventricular septal defect\n- Atrial septal defect\n- Hypertrophic cardiomyopathy\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Low-set, posteriorly rotated ears\n- Delayed speech and language development\n- Motor delay\n- Generalized hypotonia\n- Barrel-shaped chest\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Unilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Low-set, posteriorly rotated ears\n- Delayed speech and language development\n- Motor delay\n- Generalized hypotonia\n- Barrel-shaped chest\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Unilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Preauricular pit\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Preauricular pit\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- Low-set, posteriorly rotated ears\n- Long palpebral fissure\n- Autistic behavior\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- Low-set, posteriorly rotated ears\n- Long palpebral fissure\n- Autistic behavior\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Broad neck\n- Downslanted palpebral fissures\n- Ptosis\n- Blue irides\n- Pectus carinatum\n- Proportionate short stature\n- Esodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bifid uvula\n- Long face\n- Retrognathia\n- Pointed chin\n- Hypertelorism\n- Downslanted palpebral fissures\n- Proptosis\n- Bilateral ptosis\n- Macrodontia\n- High, narrow palate\n- Myopathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow nasal bridge\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thick eyebrow\n- Horizontal eyebrow\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/03226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Thick eyebrow\n- Horizontal eyebrow\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/03227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Long face\n- Thick eyebrow\n- Sparse anterior scalp hair\n- Horizontal eyebrow\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/03228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Retrognathia\n- Hypertelorism\n- Triangular face\n- Prominent supraorbital ridges\n- Long philtrum\n- Prominent nasal bridge\n- Prominent nose\n- Downslanted palpebral fissures\n- Ptosis\n- Autistic behavior\n- Intellectual disability\n- Absent speech\n- Short foot\n- Highly arched eyebrow\n- Bilateral cleft lip and palate\n- Short nose\n- Prominent nasal tip\n- Aplasia of the left hemidiaphragm\n- Short finger\n- Abnormal columella morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Retrognathia\n- Hypertelorism\n- Triangular face\n- Prominent supraorbital ridges\n- Long philtrum\n- Prominent nasal bridge\n- Prominent nose\n- Downslanted palpebral fissures\n- Ptosis\n- Autistic behavior\n- Intellectual disability\n- Absent speech\n- Short foot\n- Highly arched eyebrow\n- Bilateral cleft lip and palate\n- Short nose\n- Prominent nasal tip\n- Aplasia of the left hemidiaphragm\n- Short finger\n- Abnormal columella morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Retrognathia\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Prominent supraorbital ridges\n- Long philtrum\n- Low-set ears\n- Prominent nasal bridge\n- Prominent nose\n- Downslanted palpebral fissures\n- Ptosis\n- Long palpebral fissure\n- Bicornuate uterus\n- Umbilical hernia\n- Highly arched eyebrow\n- Short nose\n- Preauricular pit\n- Prominent nasal tip\n- Depressed nasal bridge\n- Abnormal columella morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Retrognathia\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Prominent supraorbital ridges\n- Long philtrum\n- Low-set ears\n- Prominent nasal bridge\n- Prominent nose\n- Downslanted palpebral fissures\n- Ptosis\n- Long palpebral fissure\n- Bicornuate uterus\n- Umbilical hernia\n- Highly arched eyebrow\n- Short nose\n- Preauricular pit\n- Prominent nasal tip\n- Depressed nasal bridge\n- Abnormal columella morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin vermilion border\n- Hydrocephalus\n- Retrognathia\n- Hypertelorism\n- Smooth philtrum\n- Prominent supraorbital ridges\n- Long philtrum\n- Low-set ears\n- Prominent nasal bridge\n- Prominent nose\n- Downslanted palpebral fissures\n- Glaucoma\n- Ptosis\n- Long palpebral fissure\n- Bicornuate uterus\n- Diabetes mellitus\n- Highly arched eyebrow\n- Short nose\n- Preauricular pit\n- Gastrointestinal obstruction\n- Prominent nasal tip\n- Depressed nasal bridge\n- Median cleft palate\n- Abnormal columella morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Prominent nasal bridge\n- Wide nasal bridge\n- Anteverted nares\n- Natal tooth\n- Bicornuate uterus\n- Umbilical hernia\n- Atrial septal defect\n- Short toe\n- Highly arched eyebrow\n- Short stature\n- Short finger\n- Limb undergrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Prominent nasal bridge\n- Wide nasal bridge\n- Anteverted nares\n- Natal tooth\n- Bicornuate uterus\n- Umbilical hernia\n- Atrial septal defect\n- Short toe\n- Highly arched eyebrow\n- Short stature\n- Short finger\n- Limb undergrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide anterior fontanel\n- Hypertelorism\n- Prominent supraorbital ridges\n- Wide nasal bridge\n- Webbed neck\n- Downslanted palpebral fissures\n- Hemihypertrophy\n- Omphalocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Prominent nasal bridge\n- Wide nasal bridge\n- Dysphagia\n- Mild expressive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Prominent nasal bridge\n- Wide nasal bridge\n- Dysphagia\n- Mild expressive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Large fontanelles\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Hypermetropia\n- Pectus excavatum\n- Congenital diaphragmatic hernia\n- Brachydactyly\n- Umbilical hernia\n- Polyhydramnios\n- Deep philtrum\n- Frontal bossing\n- Abnormality of the metopic suture\n- Posterior helix pit\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Highly arched eyebrow\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Autistic behavior\n- Anxiety\n- Cutis marmorata\n- Thickened skin\n- Limitation of joint mobility\n- Growth delay\n- Lower limb spasticity\n- Lower limb hyperreflexia\n- Anarthria\n- Poor appetite\n- Proximal placement of thumb\n- Intellectual disability, severe\n- Stereotypical hand wringing\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/03242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/03243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Short philtrum\n- Macrotia\n- Strabismus\n- Atypical behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Cerebellar hypoplasia\n- Gait ataxia\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Intellectual disability, moderate\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/03244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Atypical behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Gait ataxia\n- Ventriculomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/03245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent nasal bridge\n- Deeply set eye\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Gait ataxia\n- Long nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/03246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Micrognathia\n- Low-set ears\n- Global developmental delay\n- Laryngomalacia\n- Hypoplastic toenails\n- Abnormal facial shape\n- Vomiting\n- Constipation\n- Intellectual disability, moderate\n- Sleep disturbance\n- Short stature\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Micrognathia\n- Low-set ears\n- Global developmental delay\n- Laryngomalacia\n- Hypoplastic toenails\n- Abnormal facial shape\n- Vomiting\n- Constipation\n- Intellectual disability, moderate\n- Sleep disturbance\n- Short stature\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Hypotonia\n- Abnormal facial shape\n- Constipation\n- Intellectual disability, moderate\n- Elevated hepatic transaminase\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Strabismus\n- Inflexible adherence to routines or rituals\n- Hypoplastic toenails\n- Abnormal facial shape\n- Delayed CNS myelination\n- Intellectual disability, moderate\n- Dysplastic corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Micrognathia\n- Webbed neck\n- Anxiety\n- Delayed speech and language development\n- Short toe\n- Abnormal facial shape\n- Wormian bones\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Anxiety\n- Pectus carinatum\n- Arachnodactyly\n- Generalized hypotonia\n- Hypoplastic toenails\n- Abnormal facial shape\n- Intellectual disability, moderate\n- High, narrow palate\n- Kyphosis\n- Lumbar hyperlordosis\n- Short stature\n- Laryngeal web\n- Cerebral venous sinus thrombosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Low anterior hairline\n- Hypertelorism\n- Low-set ears\n- Anteverted nares\n- Downslanted palpebral fissures\n- Iris coloboma\n- Abnormal finger morphology\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Dystonia\n- Myoclonus\n- Abnormal heart morphology\n- Pes planus\n- Constipation\n- Cerebral atrophy\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Muscle fibrillation\n- Tented upper lip vermilion\n- Generalized tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypertelorism\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Single transverse palmar crease\n- Tapered finger\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Umbilical hernia\n- Constipation\n- Highly arched eyebrow\n- Prominent nasal tip\n- Apneic episodes in infancy\n- Lipomyelomeningocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Dental crowding\n- Widely spaced teeth\n- Diastema\n- Delayed speech and language development\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/03256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Narrow chest\n- Hypertrichosis\n- Large for gestational age\n- Polyhydramnios\n- Aortic regurgitation\n- Left ventricular hypertrophy\n- Hepatomegaly\n- Immunodeficiency\n- Anterior open-bite malocclusion\n- Short 1st metacarpal\n- Short 4th metacarpal\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/03257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Myopia\n- Hypertrichosis\n- Global developmental delay\n- Large for gestational age\n- Dilated cardiomyopathy\n- Pericardial effusion\n- Hepatomegaly\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- Thick vermilion border\n- Distal joint laxity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/03258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Narrow chest\n- Cutis laxa\n- Atrial septal defect\n- Patent ductus arteriosus\n- Deep plantar creases\n- Deep palmar crease\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/03259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Gingival overgrowth\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Hypertrichosis\n- Large for gestational age\n- Patent ductus arteriosus\n- Pes planus\n- Deep plantar creases\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/03260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Narrow chest\n- Hypertrichosis\n- Large for gestational age\n- Cardiomegaly\n- Deep plantar creases\n- Ventricular septal hypertrophy\n- Prominent metopic ridge\n- Deep palmar crease\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/03261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anxiety\n- Intellectual disability, mild\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/03262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/03263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/03264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/03265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/03266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/03267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Myopia\n- Diastema\n- Autism\n- Aggressive behavior\n- Single transverse palmar crease\n- Single umbilical artery\n- Seizure\n- Hip dysplasia\n- Failure to thrive\n- Pes planus\n- Unsteady gait\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Volvulus\n- Downturned corners of mouth\n- Short stature\n- Prominent nasal tip\n- Wide intermamillary distance\n- Severe expressive language delay\n- Speech apraxia\n- Oral aversion\n- Simple ear\n- Congenital shortened small intestine\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Myopia\n- Diastema\n- Autism\n- Aggressive behavior\n- Single transverse palmar crease\n- Single umbilical artery\n- Seizure\n- Hip dysplasia\n- Failure to thrive\n- Pes planus\n- Unsteady gait\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Volvulus\n- Downturned corners of mouth\n- Short stature\n- Prominent nasal tip\n- Wide intermamillary distance\n- Severe expressive language delay\n- Speech apraxia\n- Oral aversion\n- Simple ear\n- Congenital shortened small intestine\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Long eyelashes\n- Diastema\n- Autism\n- Pectus excavatum\n- Cervical ribs\n- Seizure\n- Hypotonia\n- Cerebellar vermis hypoplasia\n- Failure to thrive\n- Ventricular septal defect\n- Constipation\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Sleep disturbance\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Severe expressive language delay\n- Prominent ear helix\n- Oral aversion\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Single transverse palmar crease\n- Hypotonia\n- Global developmental delay\n- Umbilical hernia\n- Gastroesophageal reflux\n- Delayed CNS myelination\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Ectopic anus\n- Prominent nasal tip\n- Wide intermamillary distance\n- Severe expressive language delay\n- Simple ear\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Global developmental delay\n- Absent speech\n- Umbilical hernia\n- Atrial septal defect\n- Pes planus\n- Constipation\n- Apnea\n- Sleep disturbance\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Oral aversion\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal duplication\n- Wide mouth\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Anosmia\n- Downslanted palpebral fissures\n- Long eyelashes\n- Myopia\n- Diastema\n- Pectus excavatum\n- Seizure\n- Hypotonia\n- Cerebellar vermis hypoplasia\n- Absent speech\n- Failure to thrive\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Scoliosis\n- Downturned corners of mouth\n- Prominent nasal tip\n- Simple ear\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Optic disc coloboma\n- Diastema\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Dystonia\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Persistent left superior vena cava\n- Simple ear\n- Colpocephaly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Autism\n- Delayed speech and language development\n- Global developmental delay\n- Hypertonia\n- Plagiocephaly\n- Atrial septal defect\n- Patent ductus arteriosus\n- Constipation\n- Gastroesophageal reflux\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Delayed speech and language development\n- Intellectual disability, moderate\n- Cortical dysplasia\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Simple ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Astigmatism\n- Downslanted palpebral fissures\n- Long eyelashes\n- Myopia\n- Diastema\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Communicating hydrocephalus\n- Failure to thrive\n- Bicuspid aortic valve\n- Neutropenia\n- Constipation\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Oral aversion\n- Moderate hearing impairment\n- Simple ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Gastroesophageal reflux\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Oral aversion\n- Simple ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Astigmatism\n- Strabismus\n- Ptosis\n- Hypermetropia\n- Nystagmus\n- Autism\n- Anxiety\n- Delayed speech and language development\n- Single transverse palmar crease\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Polyphagia\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Urinary incontinence\n- Wide mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Abnormal repetitive mannerisms\n- Urticaria\n- Seizure\n- Absent speech\n- Failure to thrive\n- Constipation\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Recurrent infections\n- Clinodactyly of the 5th finger\n- Short stature\n- Prominent nasal tip\n- Simple ear\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Full cheeks\n- Long philtrum\n- Recurrent otitis media\n- Broad nasal tip\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Delayed speech and language development\n- Neonatal hypotonia\n- Metatarsus adductus\n- Broad-based gait\n- Expressive language delay\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Full cheeks\n- Long philtrum\n- Recurrent otitis media\n- Broad nasal tip\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Delayed speech and language development\n- Neonatal hypotonia\n- Metatarsus adductus\n- Broad-based gait\n- Expressive language delay\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Abnormality of the gingiva\n- Thin vermilion border\n- Widely spaced teeth\n- Impaired social interactions\n- Anxiety\n- Seizure\n- Abnormal corpus callosum morphology\n- Dysmetria\n- Dysphagia\n- Broad-based gait\n- Clinodactyly of the 5th finger\n- Oromotor apraxia\n- Absent cupid's bow\n- Protruding tongue\n- Severe global developmental delay\n- Perimembranous ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Abnormality of the gingiva\n- Thin vermilion border\n- Widely spaced teeth\n- Impaired social interactions\n- Anxiety\n- Seizure\n- Abnormal corpus callosum morphology\n- Dysmetria\n- Dysphagia\n- Broad-based gait\n- Clinodactyly of the 5th finger\n- Oromotor apraxia\n- Absent cupid's bow\n- Protruding tongue\n- Severe global developmental delay\n- Perimembranous ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Abnormality of the gingiva\n- Thin vermilion border\n- Widely spaced teeth\n- Impaired social interactions\n- Anxiety\n- Seizure\n- Abnormal corpus callosum morphology\n- Dysmetria\n- Dysphagia\n- Broad-based gait\n- Clinodactyly of the 5th finger\n- Oromotor apraxia\n- Absent cupid's bow\n- Protruding tongue\n- Severe global developmental delay\n- Perimembranous ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Abnormality of the gingiva\n- Thin vermilion border\n- Widely spaced teeth\n- Impaired social interactions\n- Anxiety\n- Seizure\n- Abnormal corpus callosum morphology\n- Dysmetria\n- Dysphagia\n- Broad-based gait\n- Clinodactyly of the 5th finger\n- Oromotor apraxia\n- Absent cupid's bow\n- Protruding tongue\n- Severe global developmental delay\n- Perimembranous ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/03286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/03294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Constipation\n- Aganglionic megacolon\n- Shortening of all distal phalanges of the fingers\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hearing impairment\n- Vertebral fusion\n- Tapered humerus\n- Short stature\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/03296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Joint dislocation\n- Talipes equinovarus\n- Scoliosis\n- Vertebral fusion\n- Short stature\n- Pseudoepiphyses of the metacarpals\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/03297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pierre-Robin sequence\n- Small face\n- Anteverted nares\n- Proptosis\n- Myopia\n- Short nose\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/03298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Small face\n- Proptosis\n- Myopia\n- Short nose\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/03299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micrognathia\n- Anteverted nares\n- Cataract\n- Pes planus\n- Genu valgum\n- Short nose\n- Depressed nasal bridge\n- Bilateral sensorineural hearing impairment\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/03300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Conductive hearing impairment\n- Anteverted nares\n- Short nose\n- Depressed nasal bridge\n- Flat face\n- Optically empty vitreous\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/03301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Micrognathia\n- Sensorineural hearing impairment\n- Wide nose\n- Anteverted nares\n- Myopia\n- Retinal degeneration\n- Platyspondyly\n- Short nose\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/03302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Micrognathia\n- Sensorineural hearing impairment\n- Anteverted nares\n- Proptosis\n- Myopia\n- Short nose\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/03303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Tapered finger\n- Seizure\n- Hypotonia\n- Ventricular septal defect\n- Delayed CNS myelination\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Almond-shaped palpebral fissure\n- Aplasia\/Hypoplasia of the nails\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Triangular face\n- Strabismus\n- Myopia\n- Carious teeth\n- Osteoporosis\n- Cutis laxa\n- Hip dysplasia\n- Joint laxity\n- Pes planus\n- Highly arched eyebrow\n- Delayed skeletal maturation\n- Prominent superficial blood vessels\n- Prominent ear helix\n- Mild global developmental delay\n- Simple ear\n- Premature skin wrinkling\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/03305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Triangular face\n- Strabismus\n- Myopia\n- Carious teeth\n- Osteoporosis\n- Cutis laxa\n- Hip dysplasia\n- Joint laxity\n- Pes planus\n- Highly arched eyebrow\n- Delayed skeletal maturation\n- Prominent superficial blood vessels\n- Prominent ear helix\n- Mild global developmental delay\n- Simple ear\n- Premature skin wrinkling\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/03306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Triangular face\n- Strabismus\n- Myopia\n- Carious teeth\n- Osteoporosis\n- Cutis laxa\n- Hip dysplasia\n- Joint laxity\n- Pes planus\n- Highly arched eyebrow\n- Delayed skeletal maturation\n- Prominent superficial blood vessels\n- Prominent ear helix\n- Mild global developmental delay\n- Simple ear\n- Premature skin wrinkling\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/03307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydroureter\n- Hydronephrosis\n- Hypertelorism\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Abnormally large globe\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Toe clinodactyly\n- Bilateral tonic-clonic seizure\n- Ileus\n- Short nose\n- Shortening of all distal phalanges of the fingers\n- Median cleft palate\n- Short finger\n- Short distal phalanx of finger\n- Uplifted earlobe\n- Tented upper lip vermilion\n- Beta-EEG\n- EEG with frontal sharp waves\n- Chronic constipation\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Cupped ear\n- Thickened helices\n- Absent speech\n- Gastroesophageal reflux\n- Aganglionic megacolon\n- Supernumerary nipple\n- Abdominal distention\n- Shortening of all distal phalanges of the toes\n- Shortening of all distal phalanges of the fingers\n- Aplasia\/Hypoplasia of the nails\n- Dilatation of the renal pelvis\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Facial asymmetry\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Ptosis\n- Long palpebral fissure\n- Growth delay\n- Large fleshy ears\n- Elevated circulating alkaline phosphatase concentration\n- Clinodactyly of the 5th finger\n- Shortening of all distal phalanges of the fingers\n- Aplasia\/Hypoplasia of the nails\n- Uplifted earlobe\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Strabismus\n- Hypotonia\n- Motor delay\n- Dandy-Walker malformation\n- Muscle weakness\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Strabismus\n- Hypotonia\n- Motor delay\n- Muscle weakness\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Seizure\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Broad nail\n- Aganglionic megacolon\n- Short distal phalanx of the 5th finger\n- Short distal phalanx of the 2nd finger\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Megacystis\n- Vesicoureteral reflux\n- Hydronephrosis\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Seizure\n- Global developmental delay\n- Absent speech\n- Small nail\n- Anal atresia\n- Anal stenosis\n- Aganglionic megacolon\n- Congenital megaureter\n- Broad hallux\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal duplication\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Global developmental delay\n- Absent speech\n- Aganglionic megacolon\n- Axial hypotonia\n- Short distal phalanx of finger\n- Tented upper lip vermilion\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Short nose\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Cataract\n- Wormian bones\n- Excessive skin wrinkling on dorsum of hands and fingers\n- Corneal opacity\n- Lipodystrophy\n- Dermal translucency\n- Narrow nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/03318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Cataract\n- Wormian bones\n- Excessive skin wrinkling on dorsum of hands and fingers\n- Corneal opacity\n- Lipodystrophy\n- Dermal translucency\n- Narrow nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/03319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Broad forehead\n- Narrow nose\n- Blue sclerae\n- Osteopenia\n- Adducted thumb\n- Hand clenching\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Joint dislocation\n- Joint hypermobility\n- Intrauterine growth retardation\n- Frontal bossing\n- Decreased body weight\n- Deep palmar crease\n- Prominent veins on trunk\n- Prematurely aged appearance\n- Palmoplantar cutis laxa\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/03320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Smooth philtrum\n- Short chin\n- Long philtrum\n- Low-set ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Deeply set eye\n- Ptosis\n- Upslanted palpebral fissure\n- Atypical behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Ventricular septal defect\n- Atrial septal defect\n- Respiratory distress\n- Delayed gross motor development\n- Exaggerated cupid's bow\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Cortical dysplasia\n- Elevated circulating alkaline phosphatase concentration\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Large earlobe\n- Narrow palpebral fissure\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Low-set, posteriorly rotated ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Microdontia\n- Delayed speech and language development\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Abnormal pinna morphology\n- Bulbous nose\n- Strabismus\n- Downslanted palpebral fissures\n- Myopia\n- Microdontia\n- Single transverse palmar crease\n- Hypotonia\n- Atrial septal defect\n- Sandal gap\n- Aplasia\/Hypoplasia of the nails\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Thin upper lip vermilion\n- Brachycephaly\n- Abnormal pinna morphology\n- Bulbous nose\n- Strabismus\n- Downslanted palpebral fissures\n- Myopia\n- Microdontia\n- Single transverse palmar crease\n- Hypotonia\n- Atrial septal defect\n- Sandal gap\n- Aplasia\/Hypoplasia of the nails\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Delayed cranial suture closure\n- Aplasia\/Hypoplasia of the clavicles\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/03325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Short philtrum\n- Hearing impairment\n- Prominent nasal bridge\n- Bilateral cleft lip and palate\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/03326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormal palate morphology\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Smooth philtrum\n- High forehead\n- Hearing impairment\n- Choanal atresia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Oligodontia\n- Delayed speech and language development\n- Scoliosis\n- Clinodactyly of the 3rd finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/03327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Pointed chin\n- Depressed nasal tip\n- Deeply set eye\n- Xanthomatosis\n- Atrial septal defect\n- Aortic valve stenosis\n- Hyperbilirubinemia\n- Coronal craniosynostosis\n- Peripheral pulmonary artery stenosis\n- Intrahepatic biliary atresia\n- Prolonged neonatal jaundice\n- Prominent forehead\n- Conjunctival icterus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Pointed chin\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Large hands\n- Motor delay\n- Hoarse cry\n- Long foot\n- Neonatal hypoglycemia\n- Frontal bossing\n- Generalized neonatal hypotonia\n- Nasogastric tube feeding in infancy\n- Increased arm span\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Pointed chin\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Large hands\n- Motor delay\n- Hoarse cry\n- Long foot\n- Neonatal hypoglycemia\n- Frontal bossing\n- Generalized neonatal hypotonia\n- Nasogastric tube feeding in infancy\n- Increased arm span\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Pointed chin\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Large hands\n- Motor delay\n- Hoarse cry\n- Long foot\n- Neonatal hypoglycemia\n- Frontal bossing\n- Generalized neonatal hypotonia\n- Nasogastric tube feeding in infancy\n- Increased arm span\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Global developmental delay\n- Increased body weight\n- Accelerated skeletal maturation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Global developmental delay\n- Increased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Global developmental delay\n- Increased body weight\n- Accelerated skeletal maturation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Large fontanelles\n- Micrognathia\n- Proptosis\n- Absent eyelashes\n- Mottled pigmentation\n- Arthritis\n- Failure to thrive\n- Alopecia\n- Dermal atrophy\n- Persistent open anterior fontanelle\n- Generalized lipodystrophy\n- Narrow nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Large fontanelles\n- Micrognathia\n- Proptosis\n- Absent eyelashes\n- Mottled pigmentation\n- Arthritis\n- Failure to thrive\n- Alopecia\n- Dermal atrophy\n- Persistent open anterior fontanelle\n- Generalized lipodystrophy\n- Narrow nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow nasal ridge\n- Proptosis\n- Absent eyelashes\n- Dental crowding\n- Delayed puberty\n- Mottled pigmentation\n- Arthritis\n- Joint stiffness\n- Alopecia\n- Absent eyebrow\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- Persistent open anterior fontanelle\n- Aplastic clavicle\n- Generalized lipodystrophy\n- Osteolytic defects of the phalanges of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow nasal ridge\n- Proptosis\n- Absent eyelashes\n- Dental crowding\n- Delayed puberty\n- Mottled pigmentation\n- Arthritis\n- Joint stiffness\n- Alopecia\n- Absent eyebrow\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- Persistent open anterior fontanelle\n- Aplastic clavicle\n- Generalized lipodystrophy\n- Osteolytic defects of the phalanges of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow nasal ridge\n- Proptosis\n- Absent eyelashes\n- Dental crowding\n- Delayed puberty\n- Mottled pigmentation\n- Arthritis\n- Joint stiffness\n- Alopecia\n- Absent eyebrow\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- Persistent open anterior fontanelle\n- Aplastic clavicle\n- Generalized lipodystrophy\n- Osteolytic defects of the phalanges of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Broad face\n- Square face\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Hoarse voice\n- Sleep disturbance\n- Tented upper lip vermilion\n- Midface retrusion\n- Head-banging\n- Self-biting\n- Stereotypical hand wringing\n- Polyembolokoilamania\n- Onychotillomania\n- Self hugging\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Broad face\n- Mandibular prognathia\n- Square face\n- Myopia\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hoarse voice\n- Sleep disturbance\n- Tented upper lip vermilion\n- Midface retrusion\n- Stereotypical hand wringing\n- Polyembolokoilamania\n- Onychotillomania\n- Self hugging\n- Self-injurious behavior\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Broad face\n- Square face\n- Abnormality iris morphology\n- Myopia\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hoarse voice\n- Sleep disturbance\n- Hypercholesterolemia\n- Short stature\n- Attention deficit hyperactivity disorder\n- Midface retrusion\n- Head-banging\n- Self-biting\n- Stereotypical hand wringing\n- Polyembolokoilamania\n- Self hugging\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Low anterior hairline\n- Recurrent otitis media\n- Strabismus\n- Myopia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Hirsutism\n- Numerous nevi\n- Brachydactyly\n- Intellectual disability, mild\n- Pulmonic stenosis\n- Highly arched eyebrow\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Low anterior hairline\n- Recurrent otitis media\n- Strabismus\n- Myopia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Synophrys\n- Hirsutism\n- Numerous nevi\n- Brachydactyly\n- Intellectual disability, mild\n- Pulmonic stenosis\n- Highly arched eyebrow\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Prominent nasal bridge\n- Deeply set eye\n- Uplifted earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/03345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/03346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/03347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/03348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Hydrocephalus\n- Coarse facial features\n- Epicanthus\n- Broad forehead\n- Bulbous nose\n- Short neck\n- Strabismus\n- Hyperkeratosis\n- Ulnar deviation of the hand or of fingers of the hand\n- Seizure\n- Barrel-shaped chest\n- Redundant skin\n- Hoarse voice\n- Deep plantar creases\n- Curly hair\n- Large fleshy ears\n- Kyphoscoliosis\n- Obstructive sleep apnea\n- Depressed nasal bridge\n- Deep palmar crease\n- Widened distal phalanges\n- Sparse hair\n- Nail dystrophy\n- Thick vermilion border\n- Papilloma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/03349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Coarse facial features\n- Epicanthus\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Bulbous nose\n- Short neck\n- Ulnar deviation of the hand or of fingers of the hand\n- Barrel-shaped chest\n- Redundant skin\n- Hoarse voice\n- Deep plantar creases\n- Curly hair\n- Large fleshy ears\n- Obstructive sleep apnea\n- Depressed nasal bridge\n- Deep palmar crease\n- Widened distal phalanges\n- Sparse hair\n- Nail dystrophy\n- Thick vermilion border\n- Papilloma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/03350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Epicanthus\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Short neck\n- Strabismus\n- Nystagmus\n- Hyperkeratosis\n- Ulnar deviation of the hand or of fingers of the hand\n- Seizure\n- Barrel-shaped chest\n- Redundant skin\n- Hoarse voice\n- Deep plantar creases\n- Curly hair\n- Large fleshy ears\n- Kyphoscoliosis\n- Obstructive sleep apnea\n- Depressed nasal bridge\n- Deep palmar crease\n- Widened distal phalanges\n- Sparse hair\n- Nail dystrophy\n- Thick vermilion border\n- Papilloma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/03351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Prominent scalp veins\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Persistent open anterior fontanelle\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Prominent scalp veins\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Persistent open anterior fontanelle\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Prominent scalp veins\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Persistent open anterior fontanelle\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Prominent scalp veins\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Persistent open anterior fontanelle\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Prominent scalp veins\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Persistent open anterior fontanelle\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Small earlobe\n- Protruding ear\n- Proptosis\n- Prominent scalp veins\n- Alopecia\n- Frontal bossing\n- Reduced subcutaneous adipose tissue\n- Persistent open anterior fontanelle\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Urinary incontinence\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Absent speech\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Bowel incontinence\n- Short stature\n- Abnormal epiphyseal ossification\n- Intellectual disability, severe\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Urinary incontinence\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Absent speech\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Bowel incontinence\n- Short stature\n- Abnormal epiphyseal ossification\n- Intellectual disability, severe\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Facial asymmetry\n- Abnormal pinna morphology\n- Mixed hearing impairment\n- Coloboma\n- Postural instability\n- Tracheoesophageal fistula\n- Short stature\n- Abnormality of cardiovascular system morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/03360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Prominent nasal bridge\n- Strabismus\n- Hypermetropia\n- Coloboma\n- Motor delay\n- Postural instability\n- Morphological abnormality of the semicircular canal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/03361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micropenis\n- Hearing impairment\n- Abnormal pinna morphology\n- Absent earlobe\n- Autistic behavior\n- Intellectual disability, mild\n- Global developmental delay\n- Hyposmia\n- Bilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/03362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Coloboma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/03363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Bifid uvula\n- Abnormal pinna morphology\n- Sensorineural hearing impairment\n- Microphthalmia\n- Coloboma\n- Single transverse palmar crease\n- Hypoplasia of the semicircular canal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/03364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Prominent occiput\n- Narrow forehead\n- Micrognathia\n- High forehead\n- Low-set, posteriorly rotated ears\n- Macrotia\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Proptosis\n- Dental crowding\n- Intellectual disability\n- Bilateral ptosis\n- Failure to thrive\n- Redundant skin\n- Metatarsus adductus\n- Fair hair\n- Short nose\n- Prominent metopic ridge\n- Large earlobe\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/03365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Prominent occiput\n- Narrow forehead\n- Micrognathia\n- High forehead\n- Macrotia\n- Anteverted nares\n- Ptosis\n- Proptosis\n- Dental crowding\n- Brachydactyly\n- Intellectual disability\n- Failure to thrive\n- Fair hair\n- Prominent metopic ridge\n- Pes valgus\n- Thick anterior alveolar ridges\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/03366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Pointed chin\n- Hypertelorism\n- Facial hemangioma\n- Motor delay\n- Premature birth\n- Atrial septal defect\n- Asthma\n- High anterior hairline\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/03367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n- Severe short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/03371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- High forehead\n- Low-set ears\n- Anteverted nares\n- Intrauterine growth retardation\n- Small for gestational age\n- Severe failure to thrive\n- Severe short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/03372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- High forehead\n- Low-set ears\n- Anteverted nares\n- Intrauterine growth retardation\n- Small for gestational age\n- Severe failure to thrive\n- Severe short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/03373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Posteriorly rotated ears\n- Prominent nasal bridge\n- Bifid nasal tip\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Brachydactyly\n- Intellectual disability, mild\n- Patent ductus arteriosus\n- Highly arched eyebrow\n- Caudal appendage\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Supraumbilical raphe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/03374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/03375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Intellectual disability\n- Flexion contracture\n- Umbilical hernia\n- Abnormal heart valve morphology\n- Left ventricular hypertrophy\n- Hepatomegaly\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Small scrotum\n- Hypospadias\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Hypotonia\n- Global developmental delay\n- Growth delay\n- 2-3 toe syndactyly\n- Bilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/03377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Trigonocephaly\n- Microcephaly\n- Low anterior hairline\n- Hypertelorism\n- Facial hemangioma\n- Strabismus\n- Proptosis\n- Myopia\n- Upslanted palpebral fissure\n- Abnormal anterior chamber morphology\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Congenital hip dislocation\n- Umbilical hernia\n- Intellectual disability, profound\n- Ulnar deviation of the wrist\n- Feeding difficulties in infancy\n- Bilateral cleft palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Trigonocephaly\n- Microcephaly\n- Low anterior hairline\n- Hypertelorism\n- Facial hemangioma\n- Strabismus\n- Proptosis\n- Myopia\n- Upslanted palpebral fissure\n- Abnormal anterior chamber morphology\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Congenital hip dislocation\n- Umbilical hernia\n- Intellectual disability, profound\n- Ulnar deviation of the wrist\n- Feeding difficulties in infancy\n- Bilateral cleft palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Trigonocephaly\n- Microcephaly\n- Low anterior hairline\n- Hypertelorism\n- Facial hemangioma\n- Strabismus\n- Proptosis\n- Myopia\n- Upslanted palpebral fissure\n- Abnormal anterior chamber morphology\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Congenital hip dislocation\n- Umbilical hernia\n- Intellectual disability, profound\n- Ulnar deviation of the wrist\n- Feeding difficulties in infancy\n- Bilateral cleft palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Microcephaly\n- Low anterior hairline\n- Microretrognathia\n- Strabismus\n- Proptosis\n- Myopia\n- Upslanted palpebral fissure\n- Sacral dimple\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Intrauterine growth retardation\n- Intellectual disability, profound\n- Recurrent infections\n- Deep palmar crease\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Microcephaly\n- Low anterior hairline\n- Microretrognathia\n- Strabismus\n- Proptosis\n- Myopia\n- Upslanted palpebral fissure\n- Sacral dimple\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Intrauterine growth retardation\n- Intellectual disability, profound\n- Recurrent infections\n- Deep palmar crease\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of reproductive system physiology\n- Broad alveolar ridges\n- Trigonocephaly\n- Microcephaly\n- Microretrognathia\n- Hypertelorism\n- Facial hemangioma\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Myopia\n- Abnormal optic nerve morphology\n- Sacral dimple\n- Syndactyly\n- Hypotonia\n- Intrauterine growth retardation\n- Intellectual disability, profound\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of reproductive system physiology\n- Broad alveolar ridges\n- Trigonocephaly\n- Microcephaly\n- Microretrognathia\n- Hypertelorism\n- Facial hemangioma\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Myopia\n- Abnormal optic nerve morphology\n- Sacral dimple\n- Syndactyly\n- Hypotonia\n- Intrauterine growth retardation\n- Intellectual disability, profound\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Microcephaly\n- Microretrognathia\n- Posteriorly rotated ears\n- Anteverted nares\n- Strabismus\n- Proptosis\n- Myopia\n- Abnormal optic nerve morphology\n- Syndactyly\n- Seizure\n- Hypotonia\n- Congenital hip dislocation\n- Intrauterine growth retardation\n- Apnea\n- Neonatal respiratory distress\n- Recurrent infections\n- Depressed nasal bridge\n- Deep palmar crease\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Microcephaly\n- Microretrognathia\n- Posteriorly rotated ears\n- Anteverted nares\n- Strabismus\n- Proptosis\n- Myopia\n- Abnormal optic nerve morphology\n- Syndactyly\n- Seizure\n- Hypotonia\n- Congenital hip dislocation\n- Intrauterine growth retardation\n- Apnea\n- Neonatal respiratory distress\n- Recurrent infections\n- Depressed nasal bridge\n- Deep palmar crease\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Microcephaly\n- Microretrognathia\n- Posteriorly rotated ears\n- Anteverted nares\n- Strabismus\n- Proptosis\n- Myopia\n- Abnormal optic nerve morphology\n- Syndactyly\n- Seizure\n- Hypotonia\n- Congenital hip dislocation\n- Intrauterine growth retardation\n- Apnea\n- Neonatal respiratory distress\n- Recurrent infections\n- Depressed nasal bridge\n- Deep palmar crease\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/03387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Recurrent otitis media\n- Emotional lability\n- Anxiety\n- Cholelithiasis\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Gait disturbance\n- Obesity\n- Pes planus\n- Metatarsus adductus\n- Gastroesophageal reflux\n- EEG abnormality\n- Sleep disturbance\n- Obstructive sleep apnea\n- Prominent digit pad\n- Polyembolokoilamania\n- Onychotillomania\n- Self-injurious behavior\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent nose\n- Narrow nose\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/03389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low-set ears\n- Abnormal pinna morphology\n- Downslanted palpebral fissures\n- Aggressive behavior\n- Autistic behavior\n- Brachydactyly\n- Hypotonia\n- Recurrent infections\n- Prominent forehead\n- Severe global developmental delay\n- Allergy\n- Small, conical teeth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Choanal stenosis\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Mandibular condyle hypoplasia\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Megalocornea\n- Esotropia\n- Nystagmus\n- Optic atrophy\n- Abnormality of visual evoked potentials\n- Eruption failure\n- Hyperextensibility of the finger joints\n- Plagiocephaly\n- Umbilical hernia\n- Frontal bossing\n- Sparse scalp hair\n- Delayed epiphyseal ossification\n- Short nose\n- Persistent open anterior fontanelle\n- Depressed nasal bridge\n- Facial palsy\n- Deep cerebral white matter hyperintensities\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/03392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Nystagmus\n- Optic atrophy\n- Eruption failure\n- Joint hypermobility\n- Frontal bossing\n- Sparse scalp hair\n- Short nose\n- Persistent open anterior fontanelle\n- Depressed nasal bridge\n- Central retinal vessel vascular tortuosity\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/03393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Broad forehead\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Megalocornea\n- Shallow anterior chamber\n- Retinal arterial tortuosity\n- Sparse eyelashes\n- Eruption failure\n- Plagiocephaly\n- Umbilical hernia\n- Frontal bossing\n- Sparse scalp hair\n- Short nose\n- Persistent open anterior fontanelle\n- Depressed nasal bridge\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/03394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Open mouth\n- Coarse facial features\n- Narrow forehead\n- Long philtrum\n- Hypotonia\n- Global developmental delay\n- Left ventricular hypertrophy\n- Hepatomegaly\n- Scoliosis\n- Depressed nasal bridge\n- Glenoid fossa hypoplasia\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Short chin\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Delayed eruption of teeth\n- Delayed speech and language development\n- Insulin resistance\n- Thin skin\n- Delayed skeletal maturation\n- Lack of facial subcutaneous fat\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/03396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Short chin\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Delayed eruption of teeth\n- Delayed speech and language development\n- Insulin resistance\n- Thin skin\n- Delayed skeletal maturation\n- Lack of facial subcutaneous fat\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/03397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Short chin\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Delayed eruption of teeth\n- Delayed speech and language development\n- Insulin resistance\n- Thin skin\n- Delayed skeletal maturation\n- Lack of facial subcutaneous fat\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/03398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Hypermetropia\n- Upslanted palpebral fissure\n- Aggressive behavior\n- Single transverse palmar crease\n- Global developmental delay\n- Joint hypermobility\n- Sleep disturbance\n- Severe short stature\n- Tented upper lip vermilion\n- Overweight\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Square face\n- Short philtrum\n- High forehead\n- Aggressive behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sleep disturbance\n- Short stature\n- Tented upper lip vermilion\n- Head-banging\n- Thick vermilion border\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Square face\n- Short philtrum\n- High forehead\n- Aggressive behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sleep disturbance\n- Short stature\n- Tented upper lip vermilion\n- Head-banging\n- Thick vermilion border\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/03406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Hypertelorism\n- Wide nose\n- Torticollis\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Pectus carinatum\n- Tapered finger\n- Hypotonia\n- Plagiocephaly\n- Breech presentation\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Prominent ear helix\n- Thick vermilion border\n- Eclabion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Telecanthus\n- High axial triradius\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Telecanthus\n- High axial triradius\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Cleft palate\n- Broad philtrum\n- Hypertelorism\n- Micrognathia\n- Widow's peak\n- Posteriorly rotated ears\n- Hearing impairment\n- Prominent nasal bridge\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Umbilical hernia\n- Cardiomegaly\n- Dysphagia\n- Ventriculomegaly\n- Midline nasal groove\n- Sagittal craniosynostosis\n- Prominent metopic ridge\n- Stridor\n- Hypoxemia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Umbilical hernia\n- Highly arched eyebrow\n- Aortic root aneurysm\n- Tracheomalacia\n- Midline nasal groove\n- Prominent metopic ridge\n- Prominent forehead\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Hypertelorism\n- Micrognathia\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Congenital diaphragmatic hernia\n- Motor delay\n- Abnormal facial shape\n- Bilateral cleft lip and palate\n- Infantile axial hypotonia\n- Abnormality of the crus of the helix\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/03412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/03413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/03414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/03415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Hypertelorism\n- Short philtrum\n- Hearing impairment\n- Protruding ear\n- Prominent nasal bridge\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/03416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Hypertelorism\n- Prominent supraorbital ridges\n- Sagittal craniosynostosis\n- Broad hallux phalanx\n- Prominent forehead\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/03417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Microcephaly\n- Coarse facial features\n- Hypertelorism\n- Macrotia\n- Wide nose\n- Anteverted nares\n- Pectus carinatum\n- Large hands\n- Tapered finger\n- Motor delay\n- Absent speech\n- Hypoplasia of the corpus callosum\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Hip dislocation\n- Periventricular leukomalacia\n- Intellectual disability, severe\n- Thick vermilion border\n- Upper limb hypertonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Diabetes mellitus\n- Peripheral neuropathy\n- Lipoatrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Diabetes mellitus\n- Peripheral neuropathy\n- Lipoatrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Highly arched eyebrow\n- Caudal appendage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/03422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Hypertelorism\n- Chronic otitis media\n- Downslanted palpebral fissures\n- Ptosis\n- Delayed speech and language development\n- Craniosynostosis\n- Omphalocele\n- Tethered cord\n- Spina bifida\n- Highly arched eyebrow\n- Short stature\n- Mild conductive hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/03423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ectopic kidney\n- Hypertelorism\n- Downslanted palpebral fissures\n- Ptosis\n- Abnormal anterior chamber morphology\n- Patent ductus arteriosus\n- Highly arched eyebrow\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/03424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal cyst\n- Pointed chin\n- Bulbous nose\n- Upslanted palpebral fissure\n- Jaundice\n- Hyperbilirubinemia\n- Butterfly vertebrae\n- Peripheral pulmonary artery stenosis\n- Prominent forehead\n- Perimembranous ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Trigonocephaly\n- Retrognathia\n- Full cheeks\n- Pointed chin\n- Long philtrum\n- Hearing impairment\n- Telecanthus\n- Long palpebral fissure\n- Delayed speech and language development\n- Motor delay\n- Ventriculomegaly\n- Highly arched eyebrow\n- Prominent nasal tip\n- Prominent metopic ridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Trigonocephaly\n- Retrognathia\n- Full cheeks\n- Pointed chin\n- Long philtrum\n- Hearing impairment\n- Telecanthus\n- Long palpebral fissure\n- Delayed speech and language development\n- Motor delay\n- Ventriculomegaly\n- Highly arched eyebrow\n- Prominent nasal tip\n- Prominent metopic ridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Pointed chin\n- Long philtrum\n- Protruding ear\n- Broad nasal tip\n- Anteverted nares\n- Telecanthus\n- Abnormal sternum morphology\n- Global developmental delay\n- Bilateral ptosis\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Hyperacusis\n- Dilation of Virchow-Robin spaces\n- Anterior predominant thick cortex pachygyria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Pointed chin\n- Protruding ear\n- Telecanthus\n- Ptosis\n- Global developmental delay\n- Ventriculomegaly\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n- Thick corpus callosum\n- Dilation of Virchow-Robin spaces\n- Anterior predominant thick cortex pachygyria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormality of the nervous system\n- Postaxial hand polydactyly\n- Hypotonia\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Long hallux\n- Delayed CNS myelination\n- Abnormal pattern of respiration\n- Bilateral camptodactyly\n- Central hypoventilation\n- Tube feeding\n- Nuclear cataract\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/03430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypotonia\n- Long hallux\n- Talipes\n- Pulmonary hypoplasia\n- Gliosis\n- Delayed CNS myelination\n- Hyperextensible hand joints\n- Central hypoventilation\n- Nuclear cataract\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/03431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Spasticity\n- Cerebellar vermis hypoplasia\n- Patent ductus arteriosus\n- Overlapping toe\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Hypoplasia of the brainstem\n- Respiratory failure requiring assisted ventilation\n- Tricuspid regurgitation\n- Central hypoventilation\n- Abnormal atrial septum morphology\n- Bidirectional shunt\n- Cerebral white matter hypoplasia\n- Nuclear cataract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/03432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Myopia\n- Entropion\n- Reduced eye contact\n- Hypotonia\n- Spasticity\n- Cerebellar hypoplasia\n- Short foot\n- Hypoplastic toenails\n- Talipes\n- Neurodegeneration\n- Delayed CNS myelination\n- EEG abnormality\n- Scoliosis\n- Abnormal respiratory system physiology\n- Myoclonic spasms\n- Short palm\n- Lateral ventricle dilatation\n- Intellectual disability, severe\n- Widened subarachnoid space\n- Narrow palpebral fissure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/03433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Micrognathia\n- Sacral dimple\n- Respiratory insufficiency\n- Delayed CNS myelination\n- Respiratory arrest\n- Broad hallux\n- Abnormal digit morphology\n- Coronary artery fistula\n- Camptodactyly\n- Wide nasal ridge\n- Narrow palpebral fissure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/03434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Micrognathia\n- Wide nasal bridge\n- Single transverse palmar crease\n- Seizure\n- Hypotonia\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Hammertoe\n- Pulmonary arterial hypertension\n- Ventriculomegaly\n- Abnormal sacrum morphology\n- Pulmonary capillary hemangiomatosis\n- Broad hallux\n- Chylothorax\n- Undulate ribs\n- Bidirectional shunt\n- Camptodactyly\n- Nuclear cataract\n- Cortical cataract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/03435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Optic nerve hypoplasia\n- Delayed eruption of teeth\n- Delayed speech and language development\n- Hypertrichosis\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- High pitched voice\n- Delayed skeletal maturation\n- Abnormal aggressive, impulsive or violent behavior\n- Attention deficit hyperactivity disorder\n- High myopia\n- Periventricular white matter hyperintensities\n- Abnormal growth hormone level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary urgency\n- Urinary incontinence\n- Long neck\n- Hypermetropia\n- Esotropia\n- Delayed eruption of permanent teeth\n- Abnormal repetitive mannerisms\n- Self-mutilation\n- Delayed speech and language development\n- Hirsutism\n- Tapered finger\n- Seizure\n- Ataxia\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Pes planus\n- Constipation\n- Gray matter heterotopia\n- EEG abnormality\n- Sleep disturbance\n- Developmental regression\n- Bowing of the legs\n- First degree atrioventricular block\n- Head-banging\n- Heart murmur\n- Coronary sinus enlargement\n- Abnormal growth hormone level\n- Toenail dysplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Large fontanelles\n- Myopia\n- Autistic behavior\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Hepatomegaly\n- Fair hair\n- Clinodactyly of the 5th finger\n- Wide cranial sutures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Delayed speech and language development\n- Hypertrichosis\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertrichosis\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Conductive hearing impairment\n- Delayed speech and language development\n- Single transverse palmar crease\n- Papilledema\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Poor head control\n- Increased intracranial pressure\n- Obstructive sleep apnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Diffuse white matter abnormalities\n- Head-banging\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Pachygyria\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Abnormal corpus callosum morphology\n- Delayed closure of the anterior fontanelle\n- Hyperkinetic movements\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/03451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/03460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/03469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/03479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/03480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/03481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/03482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/03483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/03484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/03485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/03486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/03487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/03488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/03489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/03490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/03497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/03504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/03519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/03520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/03523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/03524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/03525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/03526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/03527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/03593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/03594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pachygyria\n- Thick corpus callosum\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal thorax morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Mental deterioration\n- Dystonia\n- Achalasia\n- Mild global developmental delay\n- Iron accumulation in brain\n- Abnormal astrocyte morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Mental deterioration\n- Dystonia\n- Achalasia\n- Mild global developmental delay\n- Iron accumulation in brain\n- Abnormal astrocyte morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Absent earlobe\n- Convex nasal ridge\n- Long neck\n- Proptosis\n- Hypodontia\n- Dental crowding\n- Narrow chest\n- Progressive clavicular acroosteolysis\n- Hyperpigmentation of the skin\n- Dry skin\n- Hyperkeratosis\n- Trichiasis\n- Spatulate thumbs\n- Alopecia\n- Abnormal left ventricle morphology\n- Nail dysplasia\n- Abnormality of the cervical spine\n- Abnormal humeral metaphysis morphology\n- Abnormal humeral diaphysis morphology\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- 2-4 toe cutaneous syndactyly\n- Limited elbow extension and supination\n- Persistence of primary teeth\n- Limited knee flexion\n- Prominent floating ribs\n- Sparse hair\n- Lipodystrophy\n- Bilateral coxa valga\n- 2-5 finger syndactyly\n- Prominent forehead\n- Loss of eyelashes\n- Right bundle branch block\n- Camptodactyly\n- Scaphocephaly\n- Abdominal mass\n- Clinodactyly of hallux\n- Lack of skin elasticity\n- Clavicular pseudarthrosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Absent earlobe\n- Convex nasal ridge\n- Long neck\n- Proptosis\n- Hypodontia\n- Dental crowding\n- Narrow chest\n- Progressive clavicular acroosteolysis\n- Hyperpigmentation of the skin\n- Dry skin\n- Hyperkeratosis\n- Trichiasis\n- Spatulate thumbs\n- Alopecia\n- Abnormal left ventricle morphology\n- Nail dysplasia\n- Abnormality of the cervical spine\n- Abnormal humeral metaphysis morphology\n- Abnormal humeral diaphysis morphology\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- 2-4 toe cutaneous syndactyly\n- Limited elbow extension and supination\n- Persistence of primary teeth\n- Limited knee flexion\n- Prominent floating ribs\n- Sparse hair\n- Lipodystrophy\n- Bilateral coxa valga\n- 2-5 finger syndactyly\n- Prominent forehead\n- Loss of eyelashes\n- Right bundle branch block\n- Camptodactyly\n- Scaphocephaly\n- Abdominal mass\n- Clinodactyly of hallux\n- Lack of skin elasticity\n- Clavicular pseudarthrosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Pectus carinatum\n- Intellectual disability\n- Seizure\n- Spasticity\n- Global developmental delay\n- Cerebral cortical atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Bilateral multifocal epileptiform discharges\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/03639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Cerebral atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Multifocal epileptiform discharges\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/03640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Intellectual disability\n- Global developmental delay\n- Cerebellar atrophy\n- Cerebral cortical atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Low voltage EEG\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/03641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Narrow forehead\n- Narrow chest\n- Hypertrichosis\n- Arachnodactyly\n- Intellectual disability\n- Seizure\n- Spasticity\n- Global developmental delay\n- Vomiting\n- Cerebral atrophy\n- Hyperkinetic movements\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Multifocal epileptiform discharges\n- Thick vermilion border\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/03642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Broad philtrum\n- Hypertelorism\n- Low-set ears\n- Macrotia\n- Bulbous nose\n- Downslanted palpebral fissures\n- Hypotonia\n- Failure to thrive\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Decreased circulating IgG level\n- Moderate global developmental delay\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/03648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/03687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/03711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Low anterior hairline\n- Hypertelorism\n- Smooth philtrum\n- Low-set, posteriorly rotated ears\n- Preauricular skin tag\n- Wide nasal bridge\n- Short neck\n- Congenital diaphragmatic hernia\n- Edema\n- Small for gestational age\n- Gliosis\n- Short stature\n- Hypoplastic left heart\n- Protruding tongue\n- Double outlet right ventricle with subaortic ventricular septal defect without pulmonary stenosis\n- Low APGAR score\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Elevated circulating growth hormone concentration\n- Global developmental delay\n- Specific learning disability\n- Atrial septal defect\n- Median cleft lip and palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Hearing impairment\n- Wide nasal bridge\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Lissencephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Hearing impairment\n- Wide nasal bridge\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Lissencephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Hearing impairment\n- Wide nasal bridge\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Lissencephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/03727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Narrow nose\n- Microcornea\n- obsolete Thin anteverted nares\n- Ocular hypertension\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Narrow nasal bridge\n- Narrow nose\n- Microcornea\n- Esotropia\n- Shallow anterior chamber\n- Carious teeth\n- Microdontia\n- obsolete Thin anteverted nares\n- Glaucomatous visual field defect\n- Abnormal optic disc morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Underdeveloped nasal alae\n- Anteverted nares\n- Glaucoma\n- Microphthalmia\n- Blindness\n- Hypodontia\n- Carious teeth\n- Microdontia\n- Depression\n- Anxiety\n- Gait disturbance\n- Brisk reflexes\n- Lower limb spasticity\n- Spastic gait\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Basal ganglia calcification\n- Unsteady gait\n- Leukoencephalopathy\n- Abnormal cerebral white matter morphology\n- Babinski sign\n- 2-3 toe syndactyly\n- Premature loss of teeth\n- Bipolar affective disorder\n- Reduced visual acuity\n- Low hanging columella\n- 3-5 finger syndactyly\n- Ankle clonus\n- Esodeviation\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low-set ears\n- Narrow nose\n- Strabismus\n- Hypodontia\n- Brachydactyly\n- Fragile nails\n- Sparse scalp hair\n- Enamel hypoplasia\n- Hypoplasia of the retina\n- 4-5 finger syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Narrow nose\n- Shallow anterior chamber\n- Microdontia\n- Long nose\n- Enamel hypoplasia\n- Abnormality of dental morphology\n- 4-5 finger syndactyly\n- Moderate myopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Retrognathia\n- Underdeveloped nasal alae\n- Convex nasal ridge\n- Microcornea\n- Hypermetropia\n- Microphthalmia\n- Nasolacrimal duct obstruction\n- Global developmental delay\n- Omphalocele\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Short nose\n- Sparse hair\n- Feeding difficulties in infancy\n- Low hanging columella\n- 4-5 finger syndactyly\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micrognathia\n- Abnormal nasal septum morphology\n- Microcornea\n- Diastema\n- Short toe\n- Broad hallux\n- 4-5 finger syndactyly\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Underdeveloped nasal alae\n- Microcornea\n- Carious teeth\n- Tooth malposition\n- Single transverse palmar crease\n- Short toe\n- Short finger\n- Broad hallux\n- Medial flaring of the eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Narrow nose\n- Hypoplasia of teeth\n- Brisk reflexes\n- Talipes equinovarus\n- Lower limb spasticity\n- Clonus\n- Postural instability\n- 4-5 toe syndactyly\n- Lower limb muscle weakness\n- Absent middle phalanx of 5th finger\n- Aplasia\/Hypoplasia of the middle phalanges of the toes\n- 4-5 finger syndactyly\n- Scissor gait\n- Mild myopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Micrognathia\n- Underdeveloped nasal alae\n- Microcornea\n- Ptosis\n- Microphthalmia\n- Taurodontia\n- Developmental glaucoma\n- Visual field defect\n- Syndactyly\n- Spastic tetraparesis\n- Hyperreflexia\n- Curly hair\n- Fine hair\n- Unsteady gait\n- Lower limb hyperreflexia\n- Abnormal globus pallidus morphology\n- Bilateral camptodactyly\n- Enamel hypoplasia\n- Ocular hypertension\n- Leg muscle stiffness\n- Short eyelashes\n- Ankle clonus\n- Knee clonus\n- Scissor gait\n- Esodeviation\n- Globus pallidus calcification\n- Hypoesthesia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Epicanthus\n- Hypertelorism\n- Underdeveloped nasal alae\n- Narrow nose\n- Microcornea\n- Cataract\n- Myopia\n- Microphthalmia\n- Gait disturbance\n- Patent foramen ovale\n- Hypoplasia of the corpus callosum\n- Basal ganglia calcification\n- Woolly hair\n- Global brain atrophy\n- Loss of speech\n- Dense calcifications in the cerebellar dentate nucleus\n- Scoliosis\n- Thickened calvaria\n- Absent frontal sinuses\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Enamel hypoplasia\n- Cerebral hypomyelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Underdeveloped nasal alae\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Underdeveloped nasal alae\n- Strabismus\n- Visual impairment\n- Cataract\n- Microphthalmia\n- Carious teeth\n- Microdontia\n- Amelogenesis imperfecta\n- Dry skin\n- Lymphedema\n- Brittle hair\n- Enamel hypoplasia\n- Premature loss of teeth\n- Aplasia\/Hypoplasia of the middle phalanx of the 5th finger\n- Low hanging columella\n- Cutaneous finger syndactyly\n- 4-5 finger syndactyly\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/03750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Intellectual disability, mild\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Abnormal pinna morphology\n- Macrotia\n- Conductive hearing impairment\n- Protruding ear\n- Strabismus\n- Long eyelashes\n- Intellectual disability, mild\n- Coarse hair\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Sparse hair\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Long eyelashes\n- Upslanted palpebral fissure\n- Autistic behavior\n- Phimosis\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Abnormal pyramidal sign\n- Sparse hair\n- Decreased testicular size\n- Hand muscle atrophy\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Autistic behavior\n- Coarse hair\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Sparse hair\n- Intellectual disability, severe\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Autistic behavior\n- Coarse hair\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Sparse hair\n- Intellectual disability, severe\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Abnormal heart morphology\n- Phimosis\n- Coarse hair\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Intellectual disability, borderline\n- Abnormal pyramidal sign\n- Sparse hair\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Strabismus\n- Hypermetropia\n- Phimosis\n- Coarse hair\n- Sparse lateral eyebrow\n- Intellectual disability, borderline\n- Abnormal pyramidal sign\n- Sparse hair\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Choanal atresia\n- Strabismus\n- Upslanted palpebral fissure\n- Autistic behavior\n- Anal atresia\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Sparse hair\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Prominent nose\n- Upslanted palpebral fissure\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Limited pronation\/supination of forearm\n- Sparse hair\n- Hand muscle atrophy\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Prominent nose\n- Upslanted palpebral fissure\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Limited pronation\/supination of forearm\n- Sparse hair\n- Hand muscle atrophy\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Conductive hearing impairment\n- Protruding ear\n- Upslanted palpebral fissure\n- Coarse hair\n- Intellectual disability, moderate\n- Sparse lateral eyebrow\n- Limited pronation\/supination of forearm\n- Abnormal pyramidal sign\n- Sparse hair\n- Hand muscle atrophy\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Conductive hearing impairment\n- Protruding ear\n- Upslanted palpebral fissure\n- Coarse hair\n- Intellectual disability, moderate\n- Sparse lateral eyebrow\n- Limited pronation\/supination of forearm\n- Abnormal pyramidal sign\n- Sparse hair\n- Hand muscle atrophy\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Strabismus\n- Long eyelashes\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Abnormal pyramidal sign\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Long eyelashes\n- Upslanted palpebral fissure\n- Coarse hair\n- Intellectual disability, moderate\n- Sparse lateral eyebrow\n- Abnormal pyramidal sign\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Autistic behavior\n- Skeletal muscle atrophy\n- Sparse lateral eyebrow\n- Intellectual disability, severe\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Facial hypotonia\n- Narrow nose\n- Anteverted nares\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Precocious puberty\n- Abnormality of the skin\n- Joint laxity\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Facial hypotonia\n- Intellectual disability, moderate\n- Decreased body weight\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Broad forehead\n- High forehead\n- Hearing impairment\n- Visual impairment\n- Abnormality of the skin\n- Seizure\n- Hypotonia\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Decreased body weight\n- Intellectual disability, severe\n- Mild malformation of cortical development\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Hypertelorism\n- Anteverted nares\n- Visual impairment\n- Hypotonia\n- Hypoplasia of the corpus callosum\n- Scoliosis\n- Intellectual disability, severe\n- Mild malformation of cortical development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Precocious puberty\n- Abnormality of the skin\n- Ventriculomegaly\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Bulbous nose\n- Wide nasal bridge\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Decreased body weight\n- Mild malformation of cortical development\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Anteverted nares\n- Atypical behavior\n- Intellectual disability, mild\n- Intellectual disability, moderate\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Atypical behavior\n- Intellectual disability, mild\n- Joint laxity\n- Ventriculomegaly\n- Scoliosis\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Visual impairment\n- Atypical behavior\n- Abnormality of the skin\n- Seizure\n- Hypotonia\n- Decreased body weight\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow nose\n- Atypical behavior\n- Hypotonia\n- Intellectual disability, mild\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Bulbous nose\n- Wide nasal bridge\n- Atypical behavior\n- Abnormality of the skin\n- Seizure\n- Hypotonia\n- Joint laxity\n- Intellectual disability, moderate\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Atypical behavior\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow nose\n- Precocious puberty\n- Joint laxity\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Abnormality of the skin\n- Hypotonia\n- Global developmental delay\n- Hypoplasia of the corpus callosum\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Facial hypotonia\n- Atypical behavior\n- Hypotonia\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Mild malformation of cortical development\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad forehead\n- High forehead\n- Atypical behavior\n- Hypotonia\n- Intellectual disability, moderate\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad forehead\n- High forehead\n- Anteverted nares\n- Hypotonia\n- Intellectual disability, mild\n- Ventriculomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad forehead\n- High forehead\n- Visual impairment\n- Atypical behavior\n- Hypotonia\n- Joint laxity\n- Ventriculomegaly\n- Decreased body weight\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Hearing impairment\n- Narrow nose\n- Anteverted nares\n- Visual impairment\n- Hypotonia\n- Hypoplasia of the corpus callosum\n- Decreased body weight\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Abnormality of the skin\n- Hypotonia\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Facial hypotonia\n- Narrow nose\n- Anteverted nares\n- Atypical behavior\n- Precocious puberty\n- Abnormality of the skin\n- Seizure\n- Hypotonia\n- Joint laxity\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the skin\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n- Intellectual disability, moderate\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Narrow nose\n- Atypical behavior\n- Hypotonia\n- Intellectual disability, moderate\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Visual impairment\n- Seizure\n- Hypotonia\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Scoliosis\n- Decreased body weight\n- Intellectual disability, severe\n- Abnormality of movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/03791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Tapered finger\n- Hypotonia\n- Generalized hypotonia\n- Failure to thrive\n- Intellectual disability, moderate\n- Hyperbilirubinemia\n- Clinodactyly of the 5th finger\n- Secondary microcephaly\n- Laryngeal stridor\n- Localized hirsutism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Micrognathia\n- Protruding ear\n- Wide nose\n- Anteverted nares\n- Downslanted palpebral fissures\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Abnormality of the cardiovascular system\n- Atrial septal defect\n- Frontal bossing\n- Intellectual disability, moderate\n- Scoliosis\n- Kyphosis\n- Short stature\n- Abnormality of the palmar creases\n- Everted upper lip vermilion\n- Intellectual disability, severe\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Abnormal sternum morphology\n- Tapered finger\n- Frontal bossing\n- Scoliosis\n- Kyphosis\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Micrognathia\n- Sensorineural hearing impairment\n- Wide nose\n- Anteverted nares\n- Downslanted palpebral fissures\n- Abnormal sternum morphology\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Scoliosis\n- Kyphosis\n- Short stature\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Wide nose\n- Anteverted nares\n- Downslanted palpebral fissures\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Intellectual disability, moderate\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Micrognathia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Widely spaced teeth\n- Abnormal sternum morphology\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Frontal bossing\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Protruding ear\n- Wide nose\n- Anteverted nares\n- Downslanted palpebral fissures\n- Abnormal sternum morphology\n- Tapered finger\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Scoliosis\n- Kyphosis\n- Short stature\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Everted lower lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Micrognathia\n- Protruding ear\n- Anteverted nares\n- Tapered finger\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Intellectual disability, moderate\n- Scoliosis\n- Kyphosis\n- Depressed nasal bridge\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Wide nose\n- Anteverted nares\n- Tapered finger\n- Intellectual disability, mild\n- Global developmental delay\n- Scoliosis\n- Kyphosis\n- Attention deficit hyperactivity disorder\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Bifid uvula\n- Microcephaly\n- Conductive hearing impairment\n- Ptosis\n- Hypodontia\n- Abnormality of the nervous system\n- Delayed speech and language development\n- Pectus carinatum\n- Tapered finger\n- Global developmental delay\n- Broad finger\n- Laryngomalacia\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Supernumerary nipple\n- Scoliosis\n- Aspiration\n- Obstructive sleep apnea\n- Short stature\n- Short palpebral fissure\n- Wide nasal base\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Bifid uvula\n- Microcephaly\n- Conductive hearing impairment\n- Ptosis\n- Hypodontia\n- Abnormality of the nervous system\n- Delayed speech and language development\n- Pectus carinatum\n- Tapered finger\n- Global developmental delay\n- Broad finger\n- Laryngomalacia\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Supernumerary nipple\n- Scoliosis\n- Aspiration\n- Obstructive sleep apnea\n- Short stature\n- Short palpebral fissure\n- Wide nasal base\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Everted lower lip vermilion\n- Downslanted palpebral fissures\n- Hypodontia\n- Widely spaced teeth\n- Abnormality of the nervous system\n- Atypical behavior\n- Delayed speech and language development\n- Pectus carinatum\n- Global developmental delay\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Inverted nipples\n- Exercise intolerance\n- Short stature\n- Thick vermilion border\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Everted lower lip vermilion\n- Downslanted palpebral fissures\n- Hypodontia\n- Widely spaced teeth\n- Abnormality of the nervous system\n- Atypical behavior\n- Delayed speech and language development\n- Pectus carinatum\n- Global developmental delay\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Inverted nipples\n- Exercise intolerance\n- Short stature\n- Thick vermilion border\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/03809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypoplastic male external genitalia\n- Macroglossia\n- Thin upper lip vermilion\n- Microcephaly\n- Wide anterior fontanel\n- Dolichocephaly\n- Small face\n- Mandibular prognathia\n- Short philtrum\n- Triangular face\n- Broad forehead\n- Micrognathia\n- Low-set ears\n- Microphthalmia\n- Blue sclerae\n- Thin skin\n- Hypertrichosis\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Sparse scalp hair\n- Birth length less than 3rd percentile\n- Reduced subcutaneous adipose tissue\n- Decreased skull ossification\n- Coronal craniosynostosis\n- Ascending tubular aorta aneurysm\n- Progeroid facial appearance\n- Absent distal phalanges\n- Aplasia\/Hypoplasia of the nails\n- Microtia\n- Postnatal growth retardation\n- Abnormality of the hairline\n- Short distal phalanx of finger\n- Dermal translucency\n- Protruding tongue\n- Mild global developmental delay\n- Midface retrusion\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/03810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Pointed chin\n- Anodontia\n- Dystonia\n- Failure to thrive\n- Laryngomalacia\n- Recurrent fever\n- Gastroesophageal reflux\n- Respiratory distress\n- Opisthotonus\n- Reduced subcutaneous adipose tissue\n- Progeroid facial appearance\n- Lower limb hypertonia\n- Stridor\n- Ankle clonus\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Hypotelorism\n- Oligodontia\n- Natal tooth\n- Delayed eruption of permanent teeth\n- Thin skin\n- Prominent scalp veins\n- Flexion contracture\n- Intrauterine growth retardation\n- Frontal bossing\n- Kyphosis\n- Short stature\n- Lipodystrophy\n- Dermal translucency\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Microcephaly\n- Triangular face\n- Micrognathia\n- Hearing impairment\n- Low-set ears\n- Strabismus\n- Cataract\n- Myopia\n- Delayed speech and language development\n- Osteopenia\n- Osteoporosis\n- Thin skin\n- Prominent scalp veins\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Intrauterine growth retardation\n- Abnormal heart morphology\n- Frontal bossing\n- Sparse scalp hair\n- Abnormal cerebral white matter morphology\n- Neonatal respiratory distress\n- Corneal opacity\n- Postnatal growth retardation\n- Lipodystrophy\n- Dermal translucency\n- Premature skin wrinkling\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/03814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Long eyelashes\n- Synophrys\n- Widely spaced teeth\n- Delayed speech and language development\n- Hyperactivity\n- Growth delay\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Uplifted earlobe\n- Everted upper lip vermilion\n- Broad eyebrow\n- Moderate global developmental delay\n- Chin with horizontal crease\n- Neonatal seizure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/03815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sacral dimple\n- Small foramen magnum\n- Fused cervical vertebrae\n- Abnormality of the odontoid process\n- Elbow hypertrichosis\n- Chiari type I malformation\n- Basilar invagination\n- Pain in head and neck region\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/03817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Sparse eyelashes\n- Palmoplantar hyperkeratosis\n- Poikiloderma\n- Alopecia of scalp\n- Abnormal bone structure\n- Short stature\n- Decreased body weight\n- Patellar aplasia\n- Absent thumb\n- Erythematous macule\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Poikiloderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Malar flattening\n- Small face\n- Long face\n- Protruding ear\n- Upslanted palpebral fissure\n- Hypernasal speech\n- Situs inversus totalis\n- Short stature\n- Decreased body weight\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Malar flattening\n- Small face\n- Long face\n- Mandibular prognathia\n- Slender build\n- Hypernasal speech\n- Anal atresia\n- Intellectual disability, moderate\n- Thoracic scoliosis\n- Decreased body weight\n- Abnormality of the anus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- High palate\n- Microcephaly\n- Small face\n- Long face\n- Macrotia\n- Protruding ear\n- Upslanted palpebral fissure\n- Slender build\n- Short stature\n- Bilateral sensorineural hearing impairment\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- High palate\n- Velopharyngeal insufficiency\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Small face\n- Long face\n- Mandibular prognathia\n- Iris coloboma\n- Growth delay\n- Slender build\n- Hypernasal speech\n- Intellectual disability, moderate\n- Decreased body weight\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Round face\n- Downslanted palpebral fissures\n- Global developmental delay\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- High palate\n- Microcephaly\n- Malar flattening\n- Small face\n- Long face\n- Micrognathia\n- Abnormal pinna morphology\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Slender build\n- Tetralogy of Fallot\n- Intellectual disability, profound\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- High palate\n- Microcephaly\n- Malar flattening\n- Small face\n- Long face\n- Mandibular prognathia\n- Round face\n- Micrognathia\n- Abnormal pinna morphology\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Slender build\n- Tetralogy of Fallot\n- Intellectual disability, profound\n- Elbow flexion contracture\n- Short stature\n- Decreased body weight\n- Knee flexion contracture\n- Testicular neoplasm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/03826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Retrognathia\n- Dental malocclusion\n- Osteopenia\n- Cutaneous photosensitivity\n- Hypermelanotic macule\n- Growth delay\n- Small for gestational age\n- Recurrent fractures\n- Limited elbow movement\n- Sparse eyebrow\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Hyperpigmentation of the skin\n- Cutaneous photosensitivity\n- Poikiloderma\n- Failure to thrive\n- Small for gestational age\n- Chronic diarrhea\n- Short nose\n- Birth length less than 3rd percentile\n- Dermal atrophy\n- Short forearm\n- Absent thumb\n- Sparse eyebrow\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Hyperpigmentation of the skin\n- Cutaneous photosensitivity\n- Poikiloderma\n- Failure to thrive\n- Small for gestational age\n- Chronic diarrhea\n- Short nose\n- Birth length less than 3rd percentile\n- Dermal atrophy\n- Short forearm\n- Absent thumb\n- Sparse eyebrow\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/03829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft soft palate\n- Full cheeks\n- Hypertelorism\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Broad nasal tip\n- Long palpebral fissure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Broad-based gait\n- Unsteady gait\n- Elevated circulating alkaline phosphatase concentration\n- Relative macrocephaly\n- Intracranial cystic lesion\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Shoulder dystocia\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Full cheeks\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Large for gestational age\n- Elevated circulating alkaline phosphatase concentration\n- Sparse lateral eyebrow\n- Tented upper lip vermilion\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft soft palate\n- Full cheeks\n- Hypertelorism\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Hypotonia\n- Dandy-Walker malformation\n- Absent speech\n- Elevated circulating alkaline phosphatase concentration\n- Relative macrocephaly\n- Focal-onset seizure\n- Tented upper lip vermilion\n- Blake's pouch cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/03832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Facial asymmetry\n- Protruding ear\n- Hyperpigmentation of the skin\n- Omphalocele\n- Toe syndactyly\n- Patchy alopecia\n- Kyphoscoliosis\n- Finger syndactyly\n- Focal dermal aplasia\/hypoplasia\n- Sparse hair\n- Nail dystrophy\n- Midface retrusion\n- Distributed along Blaschko lines\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Facial asymmetry\n- Low-set ears\n- Widely spaced teeth\n- Hypopigmentation of the skin\n- Hypopigmented skin patches\n- Ridged nail\n- Split foot\n- Short stature\n- Dermal atrophy\n- 3-4 finger syndactyly\n- Osteopathia striata\n- Distributed along Blaschko lines\n- Clinodactyly\n- Telangiectasia of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Facial asymmetry\n- Hypopigmentation of the skin\n- Distributed along Blaschko lines\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Wide nasal bridge\n- Chorioretinal coloboma\n- Microphthalmia\n- Atrophic scars\n- Patent ductus arteriosus\n- Absent toenail\n- Scoliosis\n- 3-4 toe syndactyly\n- Short palpebral fissure\n- Ectrodactyly\n- Skin vesicle\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Wide mouth\n- Abnormal pinna morphology\n- Short clavicles\n- Aplasia cutis congenita\n- 2-3 finger syndactyly\n- Global developmental delay\n- Umbilical hernia\n- Anteriorly placed anus\n- Alopecia\n- Anonychia\n- Sparse scalp hair\n- Hypoplastic nipples\n- Genu recurvatum\n- Caudal appendage\n- Absent radius\n- Dermal atrophy\n- 2-3 toe syndactyly\n- Aplasia\/Hypoplasia of the skin\n- 3-4 toe syndactyly\n- Short distal phalanx of finger\n- Broad hallux\n- Fused nails\n- Camptodactyly\n- Bifid clitoris\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Underdeveloped nasal alae\n- Subcapsular cataract\n- Aplasia cutis congenita\n- 2-3 finger syndactyly\n- Short foot\n- Anonychia\n- Dermal atrophy\n- Nail dystrophy\n- 3-4 toe syndactyly\n- Short hallux\n- 1-2 toe syndactyly\n- Lipoma\n- Oligodactyly\n- Erythematous macule\n- Ectrodactyly\n- Hemiatrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microphthalmia\n- Conical tooth\n- Dry skin\n- Hypopigmentation of the skin\n- 2-3 finger syndactyly\n- Joint hypermobility\n- Patent ductus arteriosus\n- Small nail\n- Split foot\n- Pterygium of nails\n- Abnormality of the vasculature\n- Short middle phalanx of the 5th finger\n- Dermal atrophy\n- Sparse hair\n- 4-5 finger syndactyly\n- Absent toe\n- Dural ectasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Microcephaly\n- Facial asymmetry\n- Deeply set eye\n- Anophthalmia\n- Short sternum\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Small for gestational age\n- Omphalocele\n- Ectopia cordis\n- Split foot\n- 2-3 toe syndactyly\n- 4-5 toe syndactyly\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Short hallux\n- Overlapping fingers\n- Bifid nose\n- Camptodactyly\n- Colpocephaly\n- Unilateral conductive hearing impairment\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Microcephaly\n- Facial asymmetry\n- Deeply set eye\n- Anophthalmia\n- Short sternum\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Small for gestational age\n- Omphalocele\n- Ectopia cordis\n- Split foot\n- 2-3 toe syndactyly\n- 4-5 toe syndactyly\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Short hallux\n- Overlapping fingers\n- Bifid nose\n- Camptodactyly\n- Colpocephaly\n- Unilateral conductive hearing impairment\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Carious teeth\n- Melanocytic nevus\n- Dystrophic toenail\n- Sparse scalp hair\n- Patchy alopecia\n- 3-4 finger syndactyly\n- Distributed along Blaschko lines\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hydrocephalus\n- Microcephaly\n- Pointed chin\n- Low-set ears\n- Chorioretinal coloboma\n- Nasolacrimal duct obstruction\n- Iris coloboma\n- Hypopigmentation of the skin\n- Syndactyly\n- Failure to thrive\n- Intrauterine growth retardation\n- Patent foramen ovale\n- Nail dysplasia\n- Patchy alopecia\n- Chiari malformation\n- Myelomeningocele\n- Dermal atrophy\n- Bilateral cryptorchidism\n- Distributed along Blaschko lines\n- Arteria lusoria\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Protruding ear\n- Nystagmus\n- Optic atrophy\n- Sparse eyelashes\n- Dry skin\n- Thin skin\n- Skin rash\n- Hypermelanotic macule\n- Syndactyly\n- Sparse scalp hair\n- Exaggerated median tongue furrow\n- Reticular hyperpigmentation\n- Finger symphalangism\n- Erythema\n- Intellectual disability, severe\n- Esodeviation\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Epicanthus\n- Low-set ears\n- Cupped ear\n- Narrow nasal bridge\n- Broad nasal tip\n- Strabismus\n- Failure to thrive\n- Omphalocele\n- Patent ductus arteriosus\n- Absent toenail\n- Gastroesophageal reflux\n- Duodenal atresia\n- Intestinal malrotation\n- Clinodactyly of the 5th finger\n- Preauricular pit\n- 2-3 toe syndactyly\n- Dystrophic fingernails\n- Fetal pyelectasis\n- Abnormal lacrimal punctum morphology\n- Distributed along Blaschko lines\n- Congenital lobar overinflation\n- Tube feeding\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/03847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Sloping forehead\n- Macrotia\n- Short nose\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Strabismus\n- Dry skin\n- Parakeratosis\n- Intellectual disability\n- Growth delay\n- Abnormal facial shape\n- Abnormal cerebral morphology\n- Enterocolitis\n- Recurrent pneumonia\n- Sparse hair\n- Granuloma\n- Recurrent upper and lower respiratory tract infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Growth delay\n- Lymphadenopathy\n- Dermal atrophy\n- Recurrent sinusitis\n- Mild global developmental delay\n- Hodgkin lymphoma\n- Non-Hodgkin lymphoma\n- Erythematous plaque\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Epicanthus\n- Sloping forehead\n- Macrotia\n- Parakeratosis\n- Prominent forehead\n- Erythematous plaque\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Epicanthus\n- Sloping forehead\n- Low-set ears\n- Anteverted nares\n- Failure to thrive\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Microretrognathia\n- Bird-like facies\n- Sloping forehead\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Recurrent skin infections\n- Pulmonary infiltrates\n- Recurrent respiratory infections\n- Long nose\n- Decreased circulating antibody level\n- Short stature\n- Decreased body weight\n- Sparse hair\n- Mild global developmental delay\n- Bronchial wall thickening\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Thin upper lip vermilion\n- Epicanthus\n- Bird-like facies\n- Sloping forehead\n- Micrognathia\n- Low-set ears\n- Macrotia\n- Narrow nose\n- Growth delay\n- Deep philtrum\n- Pulmonary infiltrates\n- Recurrent respiratory infections\n- Lymphadenopathy\n- Long nose\n- Decreased circulating antibody level\n- Decreased body weight\n- Abnormal helix morphology\n- Decreased lymphocyte proliferation in response to mitogen\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Hydronephrosis\n- Hydrocephalus\n- Microcephaly\n- Small face\n- Retrognathia\n- Bird-like facies\n- Hearing impairment\n- Low-set ears\n- Narrow nose\n- Delayed speech and language development\n- Hip dysplasia\n- Recurrent infections\n- Abnormal T cell morphology\n- Long nose\n- Short stature\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Sloping forehead\n- Protruding ear\n- Ptosis\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Abnormal posterior cranial fossa morphology\n- Global developmental delay\n- Failure to thrive\n- Small for gestational age\n- Neutropenia\n- Vomiting\n- Dysphagia\n- Pneumonia\n- Gastrointestinal hemorrhage\n- Drooling\n- Medulloblastoma\n- Birth length less than 3rd percentile\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Gastritis\n- Recurrent bacterial skin infections\n- Delayed fine motor development\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Sloping forehead\n- Long nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Primary amenorrhea\n- Delayed puberty\n- Recurrent skin infections\n- Neutropenia\n- Bronchiectasis\n- Chronic mucocutaneous candidiasis\n- Frequent Giardia lamblia infestation\n- Recurrent sinopulmonary infections\n- Recurrent pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/03860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Highly arched eyebrow\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Highly arched eyebrow\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Highly arched eyebrow\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Highly arched eyebrow\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Low-set ears\n- Downslanted palpebral fissures\n- Intellectual disability\n- Short stature\n- Low hanging columella\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Low-set ears\n- Downslanted palpebral fissures\n- Intellectual disability\n- Short stature\n- Low hanging columella\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Epicanthus\n- Overfolded helix\n- Blepharophimosis\n- Umbilical hernia\n- Supernumerary nipple\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Blepharophimosis\n- Aplasia\/Hypoplasia affecting the eye\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Epicanthus\n- Abnormality of refraction\n- Bilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Epicanthus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Epicanthus inversus\n- Blepharophimosis\n- Bilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Telecanthus\n- Epicanthus inversus\n- Blepharophimosis\n- Bilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Epicanthus\n- Nystagmus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- Intrauterine growth retardation\n- Depressed nasal bridge\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Strabismus\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- Global developmental delay\n- Metatarsus adductus\n- Depressed nasal bridge\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormal pinna morphology\n- Telecanthus\n- Ptosis\n- Microphthalmia\n- Blepharophimosis\n- Abnormal nasal morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Facial asymmetry\n- Low-set ears\n- Abnormal pinna morphology\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Microphthalmia\n- Blepharophimosis\n- Entropion\n- Flexion contracture\n- Intrauterine growth retardation\n- Deep philtrum\n- Abnormal nasal morphology\n- Postnatal growth retardation\n- Severe global developmental delay\n- Hypoplasia of eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Long philtrum\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Strabismus\n- Telecanthus\n- Ptosis\n- Abnormal eyebrow morphology\n- Epicanthus inversus\n- Hypermetropia\n- Blepharophimosis\n- Tapered finger\n- Short nose\n- Depressed nasal bridge\n- Abnormally folded helix\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Unilateral renal agenesis\n- Microcephaly\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- Hypotonia\n- Failure to thrive\n- Intrauterine growth retardation\n- Secundum atrial septal defect\n- Dysphagia\n- Depressed nasal bridge\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Low-set ears\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Short chin\n- Narrow forehead\n- Overfolded helix\n- Macrotia\n- Wide nasal bridge\n- Prominent nose\n- Astigmatism\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Myopia\n- Blepharophimosis\n- Synophrys\n- Delayed speech and language development\n- Hypermelanotic macule\n- Striae distensae\n- Prominent fingertip pads\n- Brisk reflexes\n- Flexion contracture\n- Hallux valgus\n- Highly arched eyebrow\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Depressed nasal bridge\n- Flat occiput\n- Short 5th finger\n- Increased overbite\n- Bridged palmar crease\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Macrotia\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus inversus\n- Blepharophimosis\n- Ventriculomegaly\n- Highly arched eyebrow\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Flat occiput\n- Congenital ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Chordee\n- Low-set ears\n- Thickened helices\n- Broad nasal tip\n- Anteverted nares\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- Poor wound healing\n- Global developmental delay\n- Spastic diplegia\n- Hypertonia\n- Hyperreflexia\n- Broad-based gait\n- Postural instability\n- Clumsiness\n- Unsteady gait\n- Genu valgum\n- Mild short stature\n- Leg muscle stiffness\n- Large earlobe\n- Everted antitragus\n- Webbed penis\n- obsolete Toe walking\n- Cerebral palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Telecanthus\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Umbilical hernia\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Telecanthus\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Umbilical hernia\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Anteverted nares\n- Telecanthus\n- Blepharophimosis\n- Bilateral ptosis\n- Depressed nasal bridge\n- Short palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Anteverted nares\n- Telecanthus\n- Ptosis\n- Epicanthus inversus\n- Hypermetropia\n- Microphthalmia\n- Blepharophimosis\n- Horizontal nystagmus\n- Delayed speech and language development\n- Global developmental delay\n- Esodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypoplasia of the uterus\n- High palate\n- Ptosis\n- Epicanthus inversus\n- Blepharophimosis\n- Hypergonadotropic hypogonadism\n- Congenital hip dislocation\n- Growth delay\n- Short stature\n- Decreased body weight\n- Fetal distress\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/03895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Highly arched eyebrow\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/03914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular face\n- Lacrimal duct atresia\n- Joint laxity\n- Decreased liver function\n- Abnormal heart morphology\n- Ventricular septal defect\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Talipes equinovarus\n- Butterfly vertebrae\n- Axial hypotonia\n- Prominent forehead\n- Narrow nail\n- Right aortic arch\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/03915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/03916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/03917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/03918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/03919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/03920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/03921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Telecanthus\n- Congenital knee dislocation\n- Depressed nasal bridge\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/03922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Triangular face\n- Anteverted nares\n- Proptosis\n- Blue sclerae\n- Hypoplasia of teeth\n- Frontal bossing\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/03923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Microretrognathia\n- Preauricular skin tag\n- Conductive hearing impairment\n- Wide nasal bridge\n- Wide nose\n- Choanal atresia\n- Downslanted palpebral fissures\n- Absent eyelashes\n- Lower eyelid coloboma\n- Motor delay\n- Depressed nasal bridge\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Microretrognathia\n- Preauricular skin tag\n- Conductive hearing impairment\n- Wide nasal bridge\n- Wide nose\n- Choanal atresia\n- Downslanted palpebral fissures\n- Absent eyelashes\n- Lower eyelid coloboma\n- Motor delay\n- Depressed nasal bridge\n- Microtia\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Hypoplasia of the maxilla\n- Micrognathia\n- Abnormality of the outer ear\n- Abnormality of the auditory canal\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Ptosis\n- Epicanthus inversus\n- Absent eyelashes\n- Laryngomalacia\n- Delayed pneumatization of the mastoid process\n- Microtia\n- Sunken cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/03926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin vermilion border\n- Micrognathia\n- Absent earlobe\n- Convex nasal ridge\n- Long neck\n- Proptosis\n- Hypodontia\n- Dental crowding\n- Narrow chest\n- Progressive clavicular acroosteolysis\n- Hyperpigmentation of the skin\n- Dry skin\n- Hyperkeratosis\n- Trichiasis\n- Spatulate thumbs\n- Alopecia\n- Abnormal left ventricle morphology\n- Nail dysplasia\n- Abnormality of the cervical spine\n- Abnormal humeral metaphysis morphology\n- Abnormal humeral diaphysis morphology\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- 2-4 toe cutaneous syndactyly\n- Limited elbow extension and supination\n- Persistence of primary teeth\n- Limited knee flexion\n- Prominent floating ribs\n- Sparse hair\n- Lipodystrophy\n- Bilateral coxa valga\n- 2-5 finger syndactyly\n- Prominent forehead\n- Loss of eyelashes\n- Right bundle branch block\n- Camptodactyly\n- Scaphocephaly\n- Abdominal mass\n- Clinodactyly of hallux\n- Lack of skin elasticity\n- Clavicular pseudarthrosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/03927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Hearing impairment\n- Wide nasal bridge\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Lissencephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/03928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Microcephaly\n- Coarse facial features\n- Narrow chest\n- Hypotonia\n- Global developmental delay\n- Hepatosplenomegaly\n- Failure to thrive\n- Ovoid thoracolumbar vertebrae\n- Clinodactyly of the 5th finger\n- Limb undergrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- High forehead\n- Motor delay\n- Hip dysplasia\n- Umbilical hernia\n- Talipes equinovarus\n- Hepatomegaly\n- Inability to walk\n- Abdominal distention\n- Depressed nasal bridge\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Hearing impairment\n- Wide nose\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Thick eyebrow\n- Hirsutism\n- Prominent fingertip pads\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Umbilical hernia\n- Sandal gap\n- Sparse scalp hair\n- Decreased body weight\n- Depressed nasal bridge\n- Prominent interphalangeal joints\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/03931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Posteriorly rotated ears\n- Protruding ear\n- Wide nose\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Hyperactivity\n- Hypothyroidism\n- Intellectual disability\n- Hypotonia\n- Umbilical hernia\n- Patent foramen ovale\n- Sandal gap\n- Sparse scalp hair\n- Recurrent infections\n- Delayed skeletal maturation\n- Prominent interphalangeal joints\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the distal phalanx of the 5th finger\n- Thick nasal alae\n- Feeding difficulties\n- Abnormal temper tantrums\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/03932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Hydrocele testis\n- Micropenis\n- Gingival overgrowth\n- Microcephaly\n- Long philtrum\n- Bulbous nose\n- Abnormal thorax morphology\n- Abnormality of the skeletal system\n- Hirsutism\n- Thickened skin\n- Arachnodactyly\n- Flexion contracture\n- Hepatosplenomegaly\n- Small for gestational age\n- Broad thumb\n- Moderate global developmental delay\n- Leukocyte inclusion bodies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Hydrocele testis\n- Micropenis\n- Gingival overgrowth\n- Microcephaly\n- Long philtrum\n- Bulbous nose\n- Abnormal thorax morphology\n- Abnormality of the skeletal system\n- Hirsutism\n- Thickened skin\n- Arachnodactyly\n- Flexion contracture\n- Hepatosplenomegaly\n- Small for gestational age\n- Broad thumb\n- Moderate global developmental delay\n- Leukocyte inclusion bodies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Wide nasal bridge\n- Anteverted nares\n- Thick eyebrow\n- Cyanosis\n- Plagiocephaly\n- Protuberant abdomen\n- Hepatomegaly\n- Scoliosis\n- Skull asymmetry\n- Recurrent lower respiratory tract infections\n- Hip dislocation\n- Hip contracture\n- Abnormal cheek morphology\n- Depressed nasal bridge\n- Lumbar kyphosis\n- Contracture of thumb\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Wide nasal bridge\n- Anteverted nares\n- Thick eyebrow\n- Cyanosis\n- Plagiocephaly\n- Protuberant abdomen\n- Hepatomegaly\n- Scoliosis\n- Skull asymmetry\n- Recurrent lower respiratory tract infections\n- Hip dislocation\n- Hip contracture\n- Abnormal cheek morphology\n- Depressed nasal bridge\n- Lumbar kyphosis\n- Contracture of thumb\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival overgrowth\n- Coarse facial features\n- Broad ribs\n- Dysostosis multiplex\n- Thickened skin\n- Limited elbow extension\n- Hip dislocation\n- Abnormal ilium morphology\n- Flared metaphysis\n- Abnormal form of the vertebral bodies\n- Thoracolumbar kyphosis\n- Hypoplastic vertebral bodies\n- Contracture of the distal interphalangeal joint of the fingers\n- Hip subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocephalus\n- Trigonocephaly\n- Epicanthus\n- High forehead\n- Anteverted nares\n- Optic disc pallor\n- Thick eyebrow\n- Blindness\n- Thickened cortex of long bones\n- Global developmental delay\n- Mitral regurgitation\n- Ventriculomegaly\n- Large sella turcica\n- Abnormality of the skull base\n- Recurrent upper respiratory tract infections\n- Limited elbow movement\n- Muscle stiffness\n- Tricuspid regurgitation\n- Depressed nasal bridge\n- Premature closure of fontanelles\n- Prominent metopic ridge\n- Abnormal finger phalanx morphology\n- Decreased finger mobility\n- Limited shoulder movement\n- Recurrent pneumonia\n- Short metacarpal\n- Heart murmur\n- Abnormality of the supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocephalus\n- Trigonocephaly\n- Epicanthus\n- High forehead\n- Anteverted nares\n- Optic disc pallor\n- Thick eyebrow\n- Blindness\n- Thickened cortex of long bones\n- Global developmental delay\n- Mitral regurgitation\n- Ventriculomegaly\n- Large sella turcica\n- Abnormality of the skull base\n- Recurrent upper respiratory tract infections\n- Limited elbow movement\n- Muscle stiffness\n- Tricuspid regurgitation\n- Depressed nasal bridge\n- Premature closure of fontanelles\n- Prominent metopic ridge\n- Abnormal finger phalanx morphology\n- Decreased finger mobility\n- Limited shoulder movement\n- Recurrent pneumonia\n- Short metacarpal\n- Heart murmur\n- Abnormality of the supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Anteverted nares\n- Thickened skin\n- Interphalangeal joint contracture of finger\n- Global developmental delay\n- Generalized hypotonia\n- Broad finger\n- Diastasis recti\n- Congestive heart failure\n- Pneumonia\n- Respiratory distress\n- Recurrent respiratory infections\n- J-shaped sella turcica\n- Elbow flexion contracture\n- Hip contracture\n- Depressed nasal bridge\n- Knee flexion contracture\n- Generalized bone demineralization\n- Lumbar kyphosis\n- Alveolar ridge overgrowth\n- Short finger\n- Bullet-shaped phalanges of the hand\n- Bullet-shaped toe phalanx\n- Thin eyebrow\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Narrow forehead\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Broad ribs\n- Osteoporosis\n- Dysostosis multiplex\n- Thickened skin\n- Global developmental delay\n- Craniosynostosis\n- Joint stiffness\n- Failure to thrive\n- Left ventricular hypertrophy\n- Occipital encephalocele\n- Hepatomegaly\n- Kyphoscoliosis\n- Recurrent fractures\n- Recurrent lower respiratory tract infections\n- Enlarged metaphyses\n- Ovoid vertebral bodies\n- Depressed nasal bridge\n- Flat occiput\n- Disproportionate short-limb short stature\n- Alveolar ridge overgrowth\n- Short metacarpal\n- Cone-shaped epiphyses of the phalanges of the hand\n- Palpebral thickening\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Trigonocephaly\n- Microcephaly\n- Coarse facial features\n- Narrow forehead\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Deeply set eye\n- Broad palm\n- Broad metacarpals\n- Hepatosplenomegaly\n- Overlapping toe\n- Flared iliac wing\n- Thoracolumbar scoliosis\n- Femoral bowing\n- Short long bone\n- Elevated circulating alkaline phosphatase concentration\n- Short palm\n- Contracture of thumb\n- Short metacarpal\n- Metopic synostosis\n- Mild global developmental delay\n- Spatulate ribs\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival overgrowth\n- Epicanthus\n- Microretrognathia\n- Hypertelorism\n- Periorbital fullness\n- Osteoporosis\n- Dysostosis multiplex\n- Hypotonia\n- Hepatomegaly\n- Femoral bowing\n- Short femur\n- Increased serum beta-hexosaminidase\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival overgrowth\n- High forehead\n- Periorbital fullness\n- Hypotonia\n- Global developmental delay\n- Pneumonia\n- Respiratory distress\n- Hyperbilirubinemia\n- Short long bone\n- Short femur\n- Increased serum beta-hexosaminidase\n- Depressed nasal bridge\n- Short tibia\n- Short humerus\n- Lumbar kyphosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Broad palm\n- Short palm\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Knee flexion contracture\n- Ankle flexion contracture\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Broad palm\n- Short palm\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Knee flexion contracture\n- Ankle flexion contracture\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Prominent metopic ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Short neck\n- Global developmental delay\n- Limitation of joint mobility\n- Hip dysplasia\n- Umbilical hernia\n- Recurrent respiratory infections\n- Hepatomegaly\n- Short stature\n- Lumbar kyphoscoliosis\n- Keratan sulfate excretion in urine\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Short neck\n- Global developmental delay\n- Limitation of joint mobility\n- Hip dysplasia\n- Umbilical hernia\n- Recurrent respiratory infections\n- Hepatomegaly\n- Short stature\n- Lumbar kyphoscoliosis\n- Keratan sulfate excretion in urine\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Dysostosis multiplex\n- Cyanosis\n- Hyperhidrosis\n- Flexion contracture\n- Failure to thrive\n- Congestive heart failure\n- Cardiomegaly\n- Recurrent respiratory infections\n- Hepatomegaly\n- Feeding difficulties\n- Hip subluxation\n- Abnormal cardiac ventricular function\n- Biventricular hypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Myopia\n- Dysostosis multiplex\n- Broad palm\n- Intellectual disability\n- Motor delay\n- Plagiocephaly\n- Growth delay\n- Umbilical hernia\n- Diastasis recti\n- Hoarse voice\n- Coxa valga\n- Recurrent infections\n- Kyphosis\n- Obstructive sleep apnea\n- Radial bowing\n- Ulnar bowing\n- Short palm\n- Progressive flexion contractures\n- Ulnar deviated club hands\n- Tapered metacarpals\n- Bowing of the long bones\n- Flat face\n- Hip subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Myopia\n- Dysostosis multiplex\n- Broad palm\n- Intellectual disability\n- Motor delay\n- Plagiocephaly\n- Growth delay\n- Umbilical hernia\n- Diastasis recti\n- Hoarse voice\n- Coxa valga\n- Recurrent infections\n- Kyphosis\n- Obstructive sleep apnea\n- Radial bowing\n- Ulnar bowing\n- Short palm\n- Progressive flexion contractures\n- Ulnar deviated club hands\n- Tapered metacarpals\n- Bowing of the long bones\n- Flat face\n- Hip subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Micrognathia\n- Narrow chest\n- Abnormality of the skeletal system\n- Slender finger\n- Limitation of joint mobility\n- Broad finger\n- Failure to thrive\n- Umbilical hernia\n- Narrow foot\n- Delayed gross motor development\n- Abnormality of the wrist\n- Hip contracture\n- Thoracolumbar kyphoscoliosis\n- Short stature\n- Ulnar deviated club hands\n- Knee flexion contracture\n- Bowing of the long bones\n- Axial hypotonia\n- Heart murmur\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Motor delay\n- Flexion contracture\n- Kyphosis\n- Hip dislocation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Microcephaly\n- Coarse facial features\n- Micrognathia\n- Proptosis\n- Brachydactyly\n- Hypotonia\n- Global developmental delay\n- Hyperreflexia\n- Craniosynostosis\n- Growth delay\n- Small for gestational age\n- Weak cry\n- Hoarse cry\n- Pneumonia\n- Respiratory distress\n- Ventriculomegaly\n- Hepatomegaly\n- Highly arched eyebrow\n- Short stature\n- Decreased body weight\n- Reduced bone mineral density\n- Thoracic hypoplasia\n- Depressed nasal bridge\n- Prolonged neonatal jaundice\n- Chiari type I malformation\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocele testis\n- Hypospadias\n- Nephrocalcinosis\n- Gingival overgrowth\n- Microcephaly\n- Coarse facial features\n- Micrognathia\n- Osteopenia\n- Jaundice\n- Hypotonia\n- Hyperreflexia\n- Small for gestational age\n- Left ventricular hypertrophy\n- Thrombocytopenia\n- Respiratory distress\n- Skeletal dysplasia\n- Bowing of the legs\n- Elevated circulating alkaline phosphatase concentration\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Aplasia\/hypoplasia of the extremities\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Thick eyebrow\n- Short clavicles\n- Hyperkeratosis\n- Thickened skin\n- Wrist flexion contracture\n- Flexion contracture\n- Umbilical hernia\n- Protuberant abdomen\n- Left ventricular hypertrophy\n- Achilles tendon contracture\n- Diarrhea\n- Broad-based gait\n- Coarse hair\n- Fine hair\n- Kyphosis\n- Hypoplastic iliac wing\n- Flared iliac wing\n- Elbow flexion contracture\n- Short nose\n- Hip contracture\n- Severe short stature\n- Decreased body weight\n- Beaking of vertebral bodies\n- Knee flexion contracture\n- Flattened femoral head\n- Leg muscle stiffness\n- Short finger\n- Thick vermilion border\n- Flexion contracture of finger\n- Stiff skin\n- Palpebral thickening\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival bleeding\n- Small face\n- Low-set ears\n- Macrotia\n- Protruding ear\n- Visual impairment\n- Esotropia\n- Intellectual disability\n- Ataxia\n- Spasticity\n- Global developmental delay\n- Generalized hypotonia\n- Brisk reflexes\n- Slender build\n- Truncal ataxia\n- Short stature\n- Corneal opacity\n- Ocular pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Gingival bleeding\n- Small face\n- Low-set ears\n- Macrotia\n- Protruding ear\n- Visual impairment\n- Esotropia\n- Intellectual disability\n- Ataxia\n- Spasticity\n- Global developmental delay\n- Generalized hypotonia\n- Brisk reflexes\n- Slender build\n- Truncal ataxia\n- Short stature\n- Corneal opacity\n- Ocular pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Waddling gait\n- Shallow acetabular fossae\n- Ovoid vertebral bodies\n- Increased serum beta-hexosaminidase\n- Irregular femoral epiphysis\n- Corneal opacity\n- Bilateral coxa valga\n- Flattened femoral epiphysis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dysostosis multiplex\n- Abnormal aortic valve morphology\n- Aortic regurgitation\n- Increased serum beta-hexosaminidase\n- Limited interphalangeal movement\n- Metacarpophalangeal joint contracture\n- Systolic heart murmur\n- Hand pain\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dysostosis multiplex\n- Abnormal aortic valve morphology\n- Aortic regurgitation\n- Increased serum beta-hexosaminidase\n- Short stature\n- Decreased body weight\n- Limited interphalangeal movement\n- Metacarpophalangeal joint contracture\n- Left-to-right shunt\n- Membranous ventricular septal aneurysm\n- Systolic heart murmur\n- Hand pain\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent sternum\n- Dysostosis multiplex\n- Thickened skin\n- Hip contracture\n- Increased serum beta-hexosaminidase\n- Dermal atrophy\n- Decreased finger mobility\n- Stiff finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Prominent sternum\n- Dysostosis multiplex\n- Limitation of joint mobility\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow chest\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Round face\n- Hypoplasia of the maxilla\n- Conductive hearing impairment\n- Osteopenia\n- Hip dysplasia\n- Failure to thrive\n- Growth delay\n- Abnormal foot morphology\n- Constipation\n- Delayed skeletal maturation\n- Thoracic scoliosis\n- Short stature\n- Abnormality of the temporomandibular joint\n- Feeding difficulties\n- Constrictive median neuropathy\n- Jaw pain\n- Nasogastric tube feeding\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Full cheeks\n- Joint stiffness\n- Hip contracture\n- Depressed nasal bridge\n- Knee flexion contracture\n- Limited shoulder movement\n- Joint contracture of the hand\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Full cheeks\n- Joint stiffness\n- Hip contracture\n- Depressed nasal bridge\n- Knee flexion contracture\n- Limited shoulder movement\n- Joint contracture of the hand\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Full cheeks\n- Joint stiffness\n- Hip contracture\n- Depressed nasal bridge\n- Knee flexion contracture\n- Limited shoulder movement\n- Joint contracture of the hand\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Full cheeks\n- Joint stiffness\n- Hip contracture\n- Depressed nasal bridge\n- Knee flexion contracture\n- Limited shoulder movement\n- Joint contracture of the hand\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/03980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Broad face\n- Epicanthus\n- Broad palm\n- Hepatosplenomegaly\n- Abnormality of the musculature of the upper limbs\n- Normochromic anemia\n- Short nose\n- Myopathy\n- EMG abnormality\n- Shoulder girdle muscle weakness\n- Short stature\n- Prominent nasolabial fold\n- Flexion contracture of toe\n- Decreased finger mobility\n- Limited pronation\/supination of forearm\n- Corneal opacity\n- Abnormal eye morphology\n- Overweight\n- Heart murmur\n- Systolic heart murmur\n- Ectrodactyly\n- Hypoesthesia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Dysostosis multiplex\n- Hypoplastic ilia\n- Hirsutism\n- Global developmental delay\n- Flexion contracture\n- Joint stiffness\n- Umbilical hernia\n- Psychomotor deterioration\n- Thickened calvaria\n- Large sella turcica\n- Delayed skeletal maturation\n- Short long bone\n- Ovoid vertebral bodies\n- Deformed radius\n- Broad phalanx\n- Opacification of the corneal stroma\n- Stridor\n- obsolete Psychomotor retardation\n- Scaphocephaly\n- Systolic heart murmur\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Hyperkeratosis\n- Flexion contracture\n- Hepatosplenomegaly\n- Cardiomegaly\n- Kyphoscoliosis\n- Severe short stature\n- Aortic valve calcification\n- Mitral valve calcification\n- Corneal opacity\n- Peripheral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse hair\n- Elbow flexion contracture\n- Hip contracture\n- Corneal opacity\n- Flexion contracture of finger\n- Esodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Esotropia\n- Amblyopia\n- Thickened skin\n- Soft tissue swelling of interphalangeal joints\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Hypertelorism\n- Dental malocclusion\n- Abnormal rib morphology\n- Broad clavicles\n- Hirsutism\n- Interphalangeal joint contracture of finger\n- Broad metacarpals\n- Carpal bone hypoplasia\n- Pes cavus\n- Coarse hair\n- Scoliosis\n- Coxa valga\n- Hypoplastic iliac wing\n- Disproportionate short-trunk short stature\n- Sloping radial epiphyses\n- Sloping ulnar metaphysis\n- Abnormal 3rd finger morphology\n- Short stature\n- Shortening of all metacarpals\n- Glenoid fossa hypoplasia\n- Stiff shoulders\n- Short phalanx of finger\n- Broad proximal phalanges of the hand\n- Stiff elbow\n- Stiff knee\n- Schmorl's node\n- Tip-toe gait\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Hypertelorism\n- Dental malocclusion\n- Dysostosis multiplex\n- Hirsutism\n- Thickened skin\n- Pes cavus\n- Coarse hair\n- Spondylolisthesis\n- Disproportionate short-trunk short stature\n- Short stature\n- Posterior scalloping of vertebral bodies\n- Premature ventricular contraction\n- Stiff shoulders\n- Stiff elbow\n- Stiff knee\n- Tip-toe gait\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Short chin\n- Otitis media\n- Short neck\n- Blepharitis\n- Delayed speech and language development\n- Shield chest\n- Dysostosis multiplex\n- Thickened skin\n- Limitation of joint mobility\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Diastasis recti\n- Abnormal heart morphology\n- Nasal congestion\n- Diarrhea\n- Coarse hair\n- Recurrent upper respiratory tract infections\n- Short stature\n- Corneal opacity\n- Long upper lip\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Macroglossia\n- Wide nose\n- Short neck\n- Short ribs\n- Intellectual disability\n- Motor delay\n- Diarrhea\n- Corneal opacity\n- Wide cranial sutures\n- Long upper lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Short chin\n- Short neck\n- Strabismus\n- Limitation of joint mobility\n- Joint stiffness\n- Umbilical hernia\n- Abnormal heart morphology\n- Recurrent respiratory infections\n- Short stature\n- Long upper lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Optic disc pallor\n- Visual loss\n- Corneal opacity\n- Periorbital edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/03999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hydrocele testis\n- Coarse facial features\n- Hypertelorism\n- Hirsutism\n- Hepatosplenomegaly\n- Umbilical hernia\n- Pneumonia\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Macular hyperpigmentation\n- Blue nevus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Full cheeks\n- Amblyopia\n- Synophrys\n- Limitation of joint mobility\n- Joint stiffness\n- Kyphoscoliosis\n- Depressed nasal bridge\n- Corneal opacity\n- Prominent forehead\n- Mild global developmental delay\n- Constrictive median neuropathy\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Short neck\n- Dysostosis multiplex\n- Plagiocephaly\n- Hepatosplenomegaly\n- Umbilical hernia\n- Nasal congestion\n- Abnormality of the cervical spine\n- Short stature\n- Depressed nasal bridge\n- Sleep apnea\n- Snoring\n- Otitis media with effusion\n- Rhinorrhea\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Short neck\n- Umbilical hernia\n- Ventricular hypertrophy\n- Recurrent respiratory infections\n- Lumbar hyperlordosis\n- Short stature\n- Corneal opacity\n- Short finger\n- Limb undergrowth\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Broad ribs\n- Dysostosis multiplex\n- Joint stiffness\n- Hepatosplenomegaly\n- Mitral regurgitation\n- Dyspnea\n- Sparse axillary hair\n- Sparse pubic hair\n- Abnormal vertebral morphology\n- Severe short stature\n- Intellectual disability, borderline\n- Corneal opacity\n- Foot joint contracture\n- Joint contracture of the hand\n- Concave nasal ridge\n- Spatulate ribs\n- Fatigue\n- Ectrodactyly\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Limitation of joint mobility\n- Joint stiffness\n- Abnormal heart valve morphology\n- Lumbar kyphosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Short neck\n- Hypermetropia\n- Optic disc pallor\n- Thick eyebrow\n- Hepatomegaly\n- Skeletal dysplasia\n- Recurrent infections\n- Depressed nasal bridge\n- Corneal opacity\n- Prominent forehead\n- Broad jaw\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Macrocephaly\n- Coarse facial features\n- Full cheeks\n- Hypertelorism\n- Hearing impairment\n- Short neck\n- Nasal congestion\n- Frontal bossing\n- Downturned corners of mouth\n- Shoulder flexion contracture\n- Depressed nasal bridge\n- Sleep apnea\n- Thick vermilion border\n- Snoring\n- Otitis media with effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Trismus\n- Coarse facial features\n- Anteverted nares\n- Taurodontia\n- Microdontia\n- Hepatosplenomegaly\n- Growth delay\n- Kyphosis\n- obsolete Externally rotated\/abducted legs\n- Short palm\n- Short stature\n- Beaking of vertebral bodies\n- Depressed nasal bridge\n- Thoracolumbar kyphosis\n- Pulp obliteration\n- Corneal opacity\n- Anterior open-bite malocclusion\n- Spatulate ribs\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Wide anterior fontanel\n- Coarse facial features\n- Hearing impairment\n- Mixed hearing impairment\n- Hepatosplenomegaly\n- Umbilical hernia\n- Mitral regurgitation\n- Bilateral talipes equinovarus\n- Lumbar kyphosis\n- Short finger\n- Stridor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Wide anterior fontanel\n- Coarse facial features\n- Hearing impairment\n- Mixed hearing impairment\n- Hepatosplenomegaly\n- Umbilical hernia\n- Mitral regurgitation\n- Bilateral talipes equinovarus\n- Lumbar kyphosis\n- Short finger\n- Stridor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- High palate\n- Coarse facial features\n- Hearing impairment\n- Carious teeth\n- Dysostosis multiplex\n- Pointed proximal second through fifth metacarpals\n- Joint stiffness\n- Mitral regurgitation\n- Recurrent respiratory infections\n- Hepatomegaly\n- Short stature\n- Corneal opacity\n- Dermatan sulfate excretion in urine\n- Lumbar kyphosis\n- Anterior open-bite malocclusion\n- Bullet-shaped phalanges of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Mastoiditis\n- Dolichocephaly\n- Coarse facial features\n- Depressed nasal tip\n- Wide nose\n- Delayed speech and language development\n- Hirsutism\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Recurrent respiratory infections\n- Sleep disturbance\n- Thoracolumbar kyphoscoliosis\n- Short stature\n- Slow decrease in visual acuity\n- Corneal opacity\n- Brain atrophy\n- obsolete Psychomotor retardation\n- Heart murmur\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Mastoiditis\n- Dolichocephaly\n- Coarse facial features\n- Depressed nasal tip\n- Wide nose\n- Delayed speech and language development\n- Hirsutism\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Recurrent respiratory infections\n- Sleep disturbance\n- Thoracolumbar kyphoscoliosis\n- Short stature\n- Slow decrease in visual acuity\n- Corneal opacity\n- Brain atrophy\n- obsolete Psychomotor retardation\n- Heart murmur\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mitral valve prolapse\n- Mitral regurgitation\n- Corneal opacity\n- Stiff shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mitral regurgitation\n- Corneal opacity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Coarse facial features\n- Hypotonia\n- Umbilical hernia\n- Ventriculomegaly\n- Posterior fossa cyst\n- Axial hypotonia\n- Feeding difficulties\n- Subcortical cerebral atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Low-set ears\n- Short neck\n- Visual impairment\n- Thick eyebrow\n- Widely spaced teeth\n- Pectus carinatum\n- Joint hypermobility\n- Joint stiffness\n- Hepatosplenomegaly\n- Growth delay\n- Umbilical hernia\n- Hallux valgus\n- Difficulty walking\n- Rickets\n- Kyphoscoliosis\n- Recurrent upper respiratory tract infections\n- Genu valgum\n- Abdominal distention\n- Severe short stature\n- Corneal opacity\n- Short finger\n- Abnormal skeletal morphology\n- Diastolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Low-set ears\n- Short neck\n- Visual impairment\n- Thick eyebrow\n- Widely spaced teeth\n- Pectus carinatum\n- Joint hypermobility\n- Joint stiffness\n- Hepatosplenomegaly\n- Growth delay\n- Umbilical hernia\n- Hallux valgus\n- Difficulty walking\n- Rickets\n- Kyphoscoliosis\n- Recurrent upper respiratory tract infections\n- Genu valgum\n- Abdominal distention\n- Severe short stature\n- Corneal opacity\n- Short finger\n- Abnormal skeletal morphology\n- Diastolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Stiff shoulders\n- Clubbing of fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Stiff shoulders\n- Clubbing of fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Urinary incontinence\n- Inguinal hernia\n- Ptosis\n- Delayed speech and language development\n- Pneumonia\n- Hepatomegaly\n- Bowel incontinence\n- Short stature\n- Mucopolysacchariduria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Dental malocclusion\n- Dysostosis multiplex\n- Brachydactyly\n- Abnormal carpal morphology\n- Carpal bone hypoplasia\n- Anisospondyly\n- Lumbar hyperlordosis\n- Short stature\n- Proximal tapering of metacarpals\n- Limited elbow flexion\n- Limited pronation\/supination of forearm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Dental malocclusion\n- Dysostosis multiplex\n- Brachydactyly\n- Abnormal carpal morphology\n- Carpal bone hypoplasia\n- Anisospondyly\n- Lumbar hyperlordosis\n- Short stature\n- Proximal tapering of metacarpals\n- Limited elbow flexion\n- Limited pronation\/supination of forearm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Coarse facial features\n- Dysostosis multiplex\n- Global developmental delay\n- Hepatosplenomegaly\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Coarse facial features\n- Dysostosis multiplex\n- Global developmental delay\n- Hepatosplenomegaly\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormal rib morphology\n- Dysostosis multiplex\n- Abnormal corpus callosum morphology\n- Mucopolysacchariduria\n- Bullet-shaped phalanges of the hand\n- Abnormal circulating hyaluronic acid concentration\n- Otitis media with effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Recurrent otitis media\n- Wide nose\n- Flared nostrils\n- Short neck\n- Pectus excavatum\n- Pallor\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Kyphosis\n- Elbow flexion contracture\n- Shoulder flexion contracture\n- Increased body weight\n- Knee flexion contracture\n- Thick vermilion border\n- Palpebral edema\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Recurrent otitis media\n- Wide nose\n- Flared nostrils\n- Short neck\n- Pectus excavatum\n- Pallor\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Kyphosis\n- Elbow flexion contracture\n- Shoulder flexion contracture\n- Increased body weight\n- Knee flexion contracture\n- Thick vermilion border\n- Palpebral edema\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Wide nose\n- Thick eyebrow\n- Periorbital fullness\n- Frontal bossing\n- Concave nasal ridge\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Recurrent otitis media\n- Joint stiffness\n- Growth delay\n- Chronic diarrhea\n- Recurrent upper respiratory tract infections\n- Short stature\n- Moderate hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Inguinal hernia\n- Tall stature\n- Abnormality of the anterior fontanelle\n- Macrocephaly\n- Coarse facial features\n- Macrotia\n- Short neck\n- Broad neck\n- Widely spaced teeth\n- Cafe-au-lait spot\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Dehydration\n- Diarrhea\n- Poor suck\n- Spastic paraparesis\n- Increased body weight\n- Impaired mastication\n- Hyperactive deep tendon reflexes\n- Prominent forehead\n- Severe global developmental delay\n- Ankle clonus\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Inguinal hernia\n- Tall stature\n- Abnormality of the anterior fontanelle\n- Macrocephaly\n- Coarse facial features\n- Macrotia\n- Short neck\n- Broad neck\n- Widely spaced teeth\n- Cafe-au-lait spot\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Dehydration\n- Diarrhea\n- Poor suck\n- Spastic paraparesis\n- Increased body weight\n- Impaired mastication\n- Hyperactive deep tendon reflexes\n- Prominent forehead\n- Severe global developmental delay\n- Ankle clonus\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Short neck\n- Pectus excavatum\n- Hirsutism\n- Hepatosplenomegaly\n- Apnea\n- Cough\n- Enlarged tonsils\n- Nasal flaring\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Short neck\n- Pectus excavatum\n- Hirsutism\n- Hepatosplenomegaly\n- Apnea\n- Cough\n- Enlarged tonsils\n- Nasal flaring\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Macroglossia\n- Coarse facial features\n- Full cheeks\n- Recurrent otitis media\n- Widely spaced teeth\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Limitation of joint mobility\n- Hepatosplenomegaly\n- Umbilical hernia\n- Chronic diarrhea\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Kyphosis\n- Prominent nasolabial fold\n- Depressed nasal bridge\n- Intellectual disability, severe\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Macroglossia\n- Coarse facial features\n- Full cheeks\n- Recurrent otitis media\n- Widely spaced teeth\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Limitation of joint mobility\n- Hepatosplenomegaly\n- Umbilical hernia\n- Chronic diarrhea\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Kyphosis\n- Prominent nasolabial fold\n- Depressed nasal bridge\n- Intellectual disability, severe\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Short neck\n- Motor delay\n- Absent speech\n- Protuberant abdomen\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Respiratory insufficiency\n- Asthma\n- Coarse hair\n- Kyphoscoliosis\n- Hip dislocation\n- Central apnea\n- Respiratory failure\n- Dermatan sulfate excretion in urine\n- Aspiration pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Wrist flexion contracture\n- Limited elbow extension\n- Hepatomegaly\n- Genu valgum\n- Short stature\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Otitis media\n- Sensorineural hearing impairment\n- Umbilical hernia\n- Mitral regurgitation\n- Respiratory insufficiency\n- Upper airway obstruction\n- Stridor\n- Stiff wrist\n- Stiff finger\n- Systolic heart murmur\n- Subglottic laryngitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Central scotoma\n- Papilledema\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Protuberant abdomen\n- Abnormal aortic valve morphology\n- Recurrent lower respiratory tract infections\n- Short stature\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Central scotoma\n- Papilledema\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Protuberant abdomen\n- Abnormal aortic valve morphology\n- Recurrent lower respiratory tract infections\n- Short stature\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Central scotoma\n- Papilledema\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Protuberant abdomen\n- Abnormal aortic valve morphology\n- Recurrent lower respiratory tract infections\n- Short stature\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocephalus\n- Macrocephaly\n- Wide anterior fontanel\n- Coarse facial features\n- Broad ribs\n- Spasticity\n- Spastic diplegia\n- Motor delay\n- Reduced tendon reflexes\n- Hepatosplenomegaly\n- Obesity\n- Protuberant abdomen\n- Diastasis recti\n- Abnormal mitral valve morphology\n- Frontal bossing\n- Ventriculomegaly\n- J-shaped sella turcica\n- Kyphosis\n- Short palm\n- Anterior beaking of lumbar vertebrae\n- Spatulate ribs\n- Hernia\n- Upper limb hypertonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Hearing impairment\n- Short neck\n- Glaucoma\n- Hypermetropia\n- Delayed speech and language development\n- Broad ribs\n- Carpal bone hypoplasia\n- Umbilical hernia\n- Heparan sulfate excretion in urine\n- Hepatomegaly\n- Cranial hyperostosis\n- Corneal opacity\n- Dermatan sulfate excretion in urine\n- Vertebral wedging\n- Mild neurosensory hearing impairment\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Prominent supraorbital ridges\n- Wide nose\n- Flared nostrils\n- Conical tooth\n- Short stature\n- Joint contracture of the hand\n- Limb undergrowth\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Conductive hearing impairment\n- Sensorineural hearing impairment\n- Hepatosplenomegaly\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Abnormal mitral valve morphology\n- Abnormal aortic morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Conductive hearing impairment\n- Hepatosplenomegaly\n- Umbilical hernia\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hearing impairment\n- Hepatosplenomegaly\n- Umbilical hernia\n- Abnormal mitral valve morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hearing impairment\n- Hepatosplenomegaly\n- Umbilical hernia\n- Abnormal mitral valve morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hearing impairment\n- Hepatosplenomegaly\n- Umbilical hernia\n- Congestive heart failure\n- Abnormal aortic valve morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hearing impairment\n- Umbilical hernia\n- Right ventricular hypertrophy\n- Left ventricular hypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Short neck\n- Widely spaced teeth\n- Prominent sternum\n- Thickened ribs\n- Dysostosis multiplex\n- Thickened skin\n- Global developmental delay\n- Limitation of joint mobility\n- Hepatosplenomegaly\n- Umbilical hernia\n- Protuberant abdomen\n- Chronic diarrhea\n- Heparan sulfate excretion in urine\n- Chronic rhinitis\n- Short stature\n- Decreased body weight\n- Corneal opacity\n- Dermatan sulfate excretion in urine\n- Lumbar kyphosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Short neck\n- Widely spaced teeth\n- Prominent sternum\n- Thickened ribs\n- Dysostosis multiplex\n- Thickened skin\n- Global developmental delay\n- Limitation of joint mobility\n- Hepatosplenomegaly\n- Umbilical hernia\n- Protuberant abdomen\n- Chronic diarrhea\n- Heparan sulfate excretion in urine\n- Chronic rhinitis\n- Short stature\n- Decreased body weight\n- Corneal opacity\n- Dermatan sulfate excretion in urine\n- Lumbar kyphosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Obesity\n- Small for gestational age\n- Truncal obesity\n- Constipation\n- Drooling\n- Loss of speech\n- Scoliosis\n- Kyphoscoliosis\n- Breast hypoplasia\n- Proportionate short stature\n- Accelerated skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Low hanging columella\n- Thick nasal alae\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Protruding tongue\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Obesity\n- Small for gestational age\n- Truncal obesity\n- Constipation\n- Drooling\n- Loss of speech\n- Scoliosis\n- Kyphoscoliosis\n- Breast hypoplasia\n- Proportionate short stature\n- Accelerated skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Low hanging columella\n- Thick nasal alae\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Protruding tongue\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Obesity\n- Small for gestational age\n- Truncal obesity\n- Constipation\n- Drooling\n- Loss of speech\n- Scoliosis\n- Kyphoscoliosis\n- Breast hypoplasia\n- Proportionate short stature\n- Accelerated skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Low hanging columella\n- Thick nasal alae\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Protruding tongue\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Obesity\n- Small for gestational age\n- Truncal obesity\n- Constipation\n- Drooling\n- Loss of speech\n- Scoliosis\n- Kyphoscoliosis\n- Breast hypoplasia\n- Proportionate short stature\n- Accelerated skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Low hanging columella\n- Thick nasal alae\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Protruding tongue\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Obesity\n- Small for gestational age\n- Truncal obesity\n- Constipation\n- Drooling\n- Loss of speech\n- Scoliosis\n- Kyphoscoliosis\n- Breast hypoplasia\n- Proportionate short stature\n- Accelerated skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Low hanging columella\n- Thick nasal alae\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Protruding tongue\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Obesity\n- Small for gestational age\n- Truncal obesity\n- Constipation\n- Drooling\n- Loss of speech\n- Scoliosis\n- Kyphoscoliosis\n- Breast hypoplasia\n- Proportionate short stature\n- Accelerated skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Low hanging columella\n- Thick nasal alae\n- Short metacarpal\n- Cone-shaped epiphysis\n- Short metatarsal\n- Protruding tongue\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Periorbital wrinkles\n- Autistic behavior\n- Seizure\n- Sandal gap\n- Scoliosis\n- Prominent interphalangeal joints\n- Sparse hair\n- Thick nasal alae\n- Moderate global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Smooth philtrum\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Hyperactivity\n- Eczema\n- Atopic dermatitis\n- Prominent fingertip pads\n- Sandal gap\n- Short distal phalanx of toe\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Prominent interphalangeal joints\n- Sparse hair\n- Short distal phalanx of finger\n- Thick nasal alae\n- Prominent eyelashes\n- Moderate global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Thickened nuchal skin fold\n- Aggressive behavior\n- Autistic behavior\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Global developmental delay\n- Short toe\n- Sandal gap\n- Constipation\n- Loss of speech\n- Short stature\n- Accelerated skeletal maturation\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Short metacarpal\n- Prominent eyelashes\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Downslanted palpebral fissures\n- Autistic behavior\n- Short attention span\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Bilateral ptosis\n- Large for gestational age\n- Mitral regurgitation\n- Patent foramen ovale\n- Sandal gap\n- Loss of speech\n- Hypsarrhythmia\n- Ivory epiphysis of the distal phalanx of the 5th finger\n- Short stature\n- Apneic episodes in infancy\n- Prominent interphalangeal joints\n- Sparse hair\n- Ivory epiphysis of the distal phalanx of the 2nd finger\n- Thick nasal alae\n- Short 4th metacarpal\n- Short 5th metacarpal\n- Short metacarpal\n- Stridor\n- Severe global developmental delay\n- Double aortic arch\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Periorbital wrinkles\n- Widely spaced teeth\n- Delayed speech and language development\n- Pectus excavatum\n- Sandal gap\n- Delayed skeletal maturation\n- Capillary hemangioma\n- Excessive wrinkled skin\n- Sparse hair\n- Thick nasal alae\n- Prominent eyelashes\n- Mild global developmental delay\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Periorbital wrinkles\n- Widely spaced teeth\n- Delayed speech and language development\n- Pectus excavatum\n- Sandal gap\n- Delayed skeletal maturation\n- Capillary hemangioma\n- Excessive wrinkled skin\n- Sparse hair\n- Thick nasal alae\n- Prominent eyelashes\n- Mild global developmental delay\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Periorbital wrinkles\n- Widely spaced teeth\n- Delayed speech and language development\n- Pectus excavatum\n- Sandal gap\n- Delayed skeletal maturation\n- Capillary hemangioma\n- Excessive wrinkled skin\n- Sparse hair\n- Thick nasal alae\n- Prominent eyelashes\n- Mild global developmental delay\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Joint hypermobility\n- Failure to thrive\n- Intrauterine growth retardation\n- Sandal gap\n- Decreased body weight\n- Accelerated skeletal maturation\n- Sparse hair\n- Thick nasal alae\n- Short metacarpal\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Joint hypermobility\n- Failure to thrive\n- Intrauterine growth retardation\n- Sandal gap\n- Decreased body weight\n- Accelerated skeletal maturation\n- Sparse hair\n- Thick nasal alae\n- Short metacarpal\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Joint hypermobility\n- Failure to thrive\n- Intrauterine growth retardation\n- Sandal gap\n- Decreased body weight\n- Accelerated skeletal maturation\n- Sparse hair\n- Thick nasal alae\n- Short metacarpal\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Joint hypermobility\n- Failure to thrive\n- Intrauterine growth retardation\n- Sandal gap\n- Decreased body weight\n- Accelerated skeletal maturation\n- Sparse hair\n- Thick nasal alae\n- Short metacarpal\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Hypermetropia\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Short toe\n- Frontal upsweep of hair\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Short metacarpal\n- Moderate global developmental delay\n- Narrow nasal tip\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Absent speech\n- Small for gestational age\n- Umbilical hernia\n- Sandal gap\n- Delayed skeletal maturation\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Thick nasal alae\n- Prominent eyelashes\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Atopic dermatitis\n- Prominent fingertip pads\n- Absent speech\n- Intrauterine growth retardation\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Sparse hair\n- Thick nasal alae\n- Hyperacusis\n- Prominent eyelashes\n- Moderate global developmental delay\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Broad philtrum\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Synophrys\n- Widely spaced teeth\n- Short attention span\n- Hypertrichosis\n- Seizure\n- Absent speech\n- Intrauterine growth retardation\n- Umbilical hernia\n- Short toe\n- Severe short stature\n- Decreased body weight\n- Deep palmar crease\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Prominent eyelashes\n- Broad thumb\n- Moderate global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Prominent fingertip pads\n- Seizure\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Severe global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/04096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/04097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Everted lower lip vermilion\n- Microcephaly\n- Coarse facial features\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Triangular face\n- Protruding ear\n- Anteverted nares\n- Deeply set eye\n- Broad metacarpals\n- Seizure\n- Global developmental delay\n- Absent speech\n- Growth delay\n- Talipes equinovarus\n- Hyperconvex nail\n- Cerebral atrophy\n- Inability to walk\n- Scoliosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Shortening of all metacarpals\n- Soft tissue swelling of interphalangeal joints\n- Sparse hair\n- Cone-shaped epiphysis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Everted lower lip vermilion\n- Microcephaly\n- Coarse facial features\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Triangular face\n- Protruding ear\n- Anteverted nares\n- Deeply set eye\n- Broad metacarpals\n- Seizure\n- Global developmental delay\n- Absent speech\n- Growth delay\n- Talipes equinovarus\n- Hyperconvex nail\n- Cerebral atrophy\n- Inability to walk\n- Scoliosis\n- Short palm\n- Short stature\n- Decreased body weight\n- Shortening of all metacarpals\n- Soft tissue swelling of interphalangeal joints\n- Sparse hair\n- Cone-shaped epiphysis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Coarse facial features\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Long philtrum\n- High forehead\n- Protruding ear\n- Narrow nasal bridge\n- Deeply set eye\n- Downslanted palpebral fissures\n- Abnormality of subcutaneous fat tissue\n- Seizure\n- Failure to thrive\n- Growth delay\n- Intrauterine growth retardation\n- Redundant skin\n- Abnormal heart morphology\n- Sandal gap\n- Curly hair\n- Brittle hair\n- Soft tissue swelling of interphalangeal joints\n- Follicular hyperkeratosis\n- Ichthyosis\n- Sparse hair\n- Nail dystrophy\n- Enlarged naris\n- Short metacarpal\n- Severe global developmental delay\n- Feeding difficulties\n- Thick vermilion border\n- Decreased body fat percentage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Coarse facial features\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Widely spaced teeth\n- Microdontia\n- Aggressive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Reduced eye contact\n- Failure to thrive\n- Sandal gap\n- Shortening of all metacarpals\n- Prominent interphalangeal joints\n- Sparse hair\n- Increased muscle lipid content\n- Low hanging columella\n- High anterior hairline\n- Feeding difficulties\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Triangular face\n- Low-set ears\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Anteverted nares\n- Widely spaced teeth\n- Microdontia\n- Aggressive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Reduced eye contact\n- Failure to thrive\n- Sandal gap\n- Highly arched eyebrow\n- Scoliosis\n- Shortening of all metacarpals\n- Swelling of proximal interphalangeal joints\n- Focal-onset seizure\n- Sparse hair\n- Increased muscle lipid content\n- High anterior hairline\n- Broad distal phalanx of the hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Hypospadias\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Broad philtrum\n- Hearing impairment\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Anteverted nares\n- Visual impairment\n- Ptosis\n- Thick eyebrow\n- Hirsutism\n- Seizure\n- Hypotonia\n- Absent speech\n- Growth delay\n- Umbilical hernia\n- Poor suck\n- Intellectual disability, moderate\n- Scoliosis\n- Prominent interphalangeal joints\n- Prominent eyelashes\n- Moderate global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Thick eyebrow\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Absent speech\n- Sandal gap\n- Sparse scalp hair\n- Short distal phalanx of the 5th finger\n- Depressed nasal bridge\n- Prominent interphalangeal joints\n- Thick nasal alae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Thick eyebrow\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Absent speech\n- Sandal gap\n- Sparse scalp hair\n- Short distal phalanx of the 5th finger\n- Depressed nasal bridge\n- Prominent interphalangeal joints\n- Thick nasal alae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long eyelashes\n- Thick eyebrow\n- Delayed eruption of permanent teeth\n- Eczema\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Scoliosis\n- Delayed skeletal maturation\n- Short distal phalanx of the 5th finger\n- Prominent interphalangeal joints\n- Feeding difficulties in infancy\n- Short metacarpal\n- Short metatarsal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long eyelashes\n- Thick eyebrow\n- Delayed eruption of permanent teeth\n- Eczema\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Scoliosis\n- Delayed skeletal maturation\n- Short distal phalanx of the 5th finger\n- Prominent interphalangeal joints\n- Feeding difficulties in infancy\n- Short metacarpal\n- Short metatarsal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long eyelashes\n- Thick eyebrow\n- Delayed eruption of permanent teeth\n- Eczema\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Scoliosis\n- Delayed skeletal maturation\n- Short distal phalanx of the 5th finger\n- Prominent interphalangeal joints\n- Feeding difficulties in infancy\n- Short metacarpal\n- Short metatarsal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Abnormality of the ear\n- Synophrys\n- Hyperactivity\n- Hirsutism\n- Intellectual disability\n- Seizure\n- Umbilical hernia\n- Sandal gap\n- Sparse scalp hair\n- Short distal phalanx of the 5th finger\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Thick nasal alae\n- Ivory epiphyses\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Abnormality of the ear\n- Synophrys\n- Hyperactivity\n- Hirsutism\n- Intellectual disability\n- Seizure\n- Umbilical hernia\n- Sandal gap\n- Sparse scalp hair\n- Short distal phalanx of the 5th finger\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Thick nasal alae\n- Ivory epiphyses\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Wide nose\n- Anteverted nares\n- Ptosis\n- Thick eyebrow\n- Psychosis\n- Hyperactivity\n- Eczema\n- Intellectual disability\n- Sparse scalp hair\n- Short distal phalanx of the 5th finger\n- Prominent interphalangeal joints\n- Thick nasal alae\n- Ivory epiphyses\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Wide nose\n- Delayed speech and language development\n- Hyperactivity\n- Eczema\n- Seizure\n- Hypotonia\n- Sandal gap\n- Sparse scalp hair\n- Intellectual disability, moderate\n- Recurrent infections\n- Prominent interphalangeal joints\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Renal duplication\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Wide nose\n- Ptosis\n- Long eyelashes\n- Thick eyebrow\n- Abnormality of the ear\n- Synophrys\n- Aggressive behavior\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Umbilical hernia\n- Sandal gap\n- Sparse scalp hair\n- Prominent interphalangeal joints\n- Intellectual disability, severe\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/04127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Prominent supraorbital ridges\n- Wide nose\n- Ptosis\n- Thick eyebrow\n- Atypical behavior\n- Aggressive behavior\n- Pectus excavatum\n- Heterochromia iridis\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Pes cavus\n- Supernumerary nipple\n- 2-3 toe syndactyly\n- Proximal finger joint hyperextensibility\n- Flat occiput\n- Increased dermatoglyphic whorls\n- 3-4 finger syndactyly\n- Short proximal phalanx of the 5th finger\n- Open bite\n- Self-injurious behavior\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Prominent supraorbital ridges\n- Wide nose\n- Ptosis\n- Thick eyebrow\n- Atypical behavior\n- Aggressive behavior\n- Pectus excavatum\n- Heterochromia iridis\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Pes cavus\n- Supernumerary nipple\n- 2-3 toe syndactyly\n- Proximal finger joint hyperextensibility\n- Flat occiput\n- Increased dermatoglyphic whorls\n- 3-4 finger syndactyly\n- Short proximal phalanx of the 5th finger\n- Open bite\n- Self-injurious behavior\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Low-set ears\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Small scrotum\n- Narrow forehead\n- Micrognathia\n- Low-set ears\n- Anteverted nares\n- Ptosis\n- Cataract\n- Cyanosis\n- Hypotonia\n- Hepatosplenomegaly\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Pericardial effusion\n- Annular pancreas\n- Hydrops fetalis\n- Respiratory failure\n- Feeding difficulties\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Hydronephrosis\n- High palate\n- Microcephaly\n- Full cheeks\n- Micrognathia\n- Anteverted nares\n- Short neck\n- Hypothyroidism\n- Cyanosis\n- Obesity\n- Pulmonic stenosis\n- Short toe\n- Inverted nipples\n- Increased body weight\n- Depressed nasal bridge\n- Short finger\n- Proximal placement of thumb\n- Bitemporal hollowing\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Hydrocephalus\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Intrauterine growth retardation\n- Small for gestational age\n- Abnormal heart morphology\n- Patent ductus arteriosus\n- Pneumonia\n- Respiratory insufficiency\n- Polymicrogyria\n- Short stature\n- Decreased body weight\n- Postnatal growth retardation\n- Intraventricular hemorrhage\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Ambiguous genitalia\n- Microcephaly\n- Intellectual disability\n- Hypotonia\n- Recurrent infections\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Postaxial polydactyly\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Ambiguous genitalia\n- Microcephaly\n- Intellectual disability\n- Hypotonia\n- Recurrent infections\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Postaxial polydactyly\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft soft palate\n- Broad alveolar ridges\n- Microcephaly\n- Epicanthus\n- Smooth philtrum\n- Micrognathia\n- Bulbous nose\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Delayed eruption of permanent teeth\n- Single transverse palmar crease\n- Thin skin\n- Hyperhidrosis\n- Hand clenching\n- Seizure\n- Ventriculomegaly\n- Opisthotonus\n- High, narrow palate\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Clitoral hypertrophy\n- Crumpled ear\n- Severe global developmental delay\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Abnormal pinna morphology\n- Protruding ear\n- Depressed nasal tip\n- Thin ribs\n- Intellectual disability\n- Agenesis of corpus callosum\n- Short stature\n- Decreased body weight\n- Persistent open anterior fontanelle\n- Depressed nasal bridge\n- Absence of the sacrum\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micropenis\n- Microglossia\n- Abnormal pinna morphology\n- Protruding ear\n- Depressed nasal tip\n- Thin ribs\n- Agenesis of corpus callosum\n- Growth delay\n- Rocker bottom foot\n- Overlapping toe\n- Bilateral cleft lip and palate\n- Persistent open anterior fontanelle\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Bilateral cryptorchidism\n- Cleft lower alveolar ridge\n- Absence of the sacrum\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Micropenis\n- Cleft palate\n- High palate\n- Microcephaly\n- Micrognathia\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Anteverted nares\n- Intrauterine growth retardation\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Feeding difficulties\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Broad alveolar ridges\n- High palate\n- Microcephaly\n- Epicanthus\n- Micrognathia\n- Abnormal pinna morphology\n- Anteverted nares\n- Ptosis\n- Single transverse palmar crease\n- Intellectual disability\n- Intrauterine growth retardation\n- Bradycardia\n- Apnea\n- 2-3 toe syndactyly\n- Clitoral hypertrophy\n- Postnatal growth retardation\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Broad alveolar ridges\n- High palate\n- Microcephaly\n- Epicanthus\n- Micrognathia\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Anteverted nares\n- Ptosis\n- Single transverse palmar crease\n- Intellectual disability\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Feeding difficulties\n- Premature adrenarche\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- High palate\n- Microcephaly\n- Epicanthus\n- Micrognathia\n- Abnormal pinna morphology\n- Ptosis\n- Single transverse palmar crease\n- Intellectual disability\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypospadias\n- Ambiguous genitalia\n- Vesicoureteral reflux\n- Thin vermilion border\n- Micrognathia\n- Posteriorly rotated ears\n- Depressed nasal tip\n- Hypotonia\n- Flexion contracture\n- Calcaneovalgus deformity\n- Short columella\n- Poor suck\n- Downturned corners of mouth\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Epileptic spasm\n- Severe global developmental delay\n- Postaxial polydactyly\n- Abnormal fetal skin morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypospadias\n- Ambiguous genitalia\n- Vesicoureteral reflux\n- Thin vermilion border\n- Micrognathia\n- Posteriorly rotated ears\n- Depressed nasal tip\n- Hypotonia\n- Flexion contracture\n- Calcaneovalgus deformity\n- Short columella\n- Poor suck\n- Downturned corners of mouth\n- Accelerated skeletal maturation\n- Bilateral single transverse palmar creases\n- Epileptic spasm\n- Severe global developmental delay\n- Postaxial polydactyly\n- Abnormal fetal skin morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Microcephaly\n- Epicanthus\n- Narrow forehead\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Ptosis\n- Esotropia\n- Pectus excavatum\n- Sacral dimple\n- Mottled pigmentation\n- Small thenar eminence\n- Intellectual disability\n- Plagiocephaly\n- Failure to thrive\n- Metatarsus adductus\n- Vomiting\n- Pyloric stenosis\n- Poor suck\n- Curly hair\n- 2-3 toe syndactyly\n- Finger syndactyly\n- Short 5th finger\n- Short thumb\n- Enlarged naris\n- Short 5th toe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Abnormal oral frenulum morphology\n- High palate\n- Microcephaly\n- Epicanthus\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Cataract\n- Hyperpigmentation of the skin\n- Sacral dimple\n- Hypertrichosis\n- Absent lacrimal punctum\n- Talipes equinovalgus\n- Apnea\n- Severe short stature\n- Short stature\n- 2-3 toe syndactyly\n- Multiple cafe-au-lait spots\n- Limb undergrowth\n- Everted upper lip vermilion\n- Feeding difficulties\n- Postaxial polydactyly\n- Epidermoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Low-set ears\n- Chronic otitis media\n- Anteverted nares\n- Ptosis\n- Hypermetropia\n- Dental crowding\n- Hypernasal speech\n- Pes cavus\n- Talipes equinovalgus\n- Patchy alopecia\n- High, narrow palate\n- Short stature\n- 2-3 toe syndactyly\n- Microtia\n- Skin tags\n- Increased overbite\n- Postaxial polydactyly\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- High palate\n- Micrognathia\n- Posteriorly rotated ears\n- Hearing impairment\n- Chronic otitis media\n- Ptosis\n- Single transverse palmar crease\n- Talipes equinovalgus\n- Hallux valgus\n- Scoliosis\n- 2-3 toe syndactyly\n- Rotated maxillary central incisors\n- Intellectual disability, borderline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypospadias\n- Bifid scrotum\n- Cleft soft palate\n- Microcephaly\n- Micrognathia\n- Prominent nasal bridge\n- Anteverted nares\n- Hypotonia\n- Global developmental delay\n- Atrial septal defect\n- Decreased body weight\n- 2-3 toe syndactyly\n- Metopic synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Generalized hypotonia\n- Coarctation of aorta\n- 2-3 toe syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Abnormal pinna morphology\n- Anteverted nares\n- Short neck\n- Ptosis\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Bifid uvula\n- Thin vermilion border\n- Microcephaly\n- Epicanthus\n- Sloping forehead\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Anteverted nares\n- Developmental cataract\n- Neonatal hypotonia\n- Subcutaneous nodule\n- Bilateral ptosis\n- Severe failure to thrive\n- Hepatomegaly\n- 2-3 toe syndactyly\n- Hallux varus\n- Midline notch of upper alveolar ridge\n- Postaxial polydactyly\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Aggressive behavior\n- Hypertonia\n- Absent speech\n- Flexion contracture\n- Hip dislocation\n- Decreased body weight\n- Pes valgus\n- Infantile muscular hypotonia\n- Elevated circulating alanine aminotransferase concentration\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypogonadotropic hypogonadism\n- Ambiguous genitalia\n- Gingival overgrowth\n- Microcephaly\n- Micrognathia\n- Cataract\n- Hypertension\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Severe failure to thrive\n- Oligohydramnios\n- Weak cry\n- Patent ductus arteriosus\n- Metatarsus adductus\n- Gastroesophageal reflux\n- Cerebral atrophy\n- Delayed skeletal maturation\n- Elbow flexion contracture\n- 2-3 toe syndactyly\n- Knee flexion contracture\n- Pes valgus\n- Radial deviation of finger\n- Colpocephaly\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Downslanted palpebral fissures\n- Ptosis\n- Specific learning disability\n- Bilateral ptosis\n- Talipes equinovalgus\n- 2-3 toe syndactyly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Anteverted nares\n- Ptosis\n- Global developmental delay\n- Failure to thrive\n- Hip dislocation\n- Short nose\n- 2-3 toe syndactyly\n- Short thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Anteverted nares\n- Ptosis\n- Short nose\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Micrognathia\n- Posteriorly rotated ears\n- Ptosis\n- Global developmental delay\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Abnormality of the palmar creases\n- Delayed myelination\n- Upper limb hypertonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Sloping forehead\n- Micrognathia\n- Low-set ears\n- Recurrent otitis media\n- Wide nose\n- Anteverted nares\n- Ptosis\n- Hypotonia\n- Spasticity\n- Muscle weakness\n- Absent speech\n- Small for gestational age\n- Vomiting\n- Motor deterioration\n- Developmental regression\n- Areflexia of lower limbs\n- Thoracic scoliosis\n- Short stature\n- 2-3 toe syndactyly\n- Recurrent pneumonia\n- Severe photosensitivity\n- Solar urticaria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Small scrotum\n- Hypospadias\n- Bifid scrotum\n- Ambiguous genitalia\n- Renal agenesis\n- Microcephaly\n- Retrognathia\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Short neck\n- Ptosis\n- Adrenal hypoplasia\n- Single transverse palmar crease\n- Intrauterine growth retardation\n- Oligohydramnios\n- Atrial septal defect\n- Patent ductus arteriosus\n- Aortic valve stenosis\n- Talipes equinovarus\n- Overlapping toe\n- Toe clinodactyly\n- Hypoplasia of the corpus callosum\n- Pulmonary arterial hypertension\n- Limb joint contracture\n- Short stature\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Broad hallux\n- Short hallux\n- Abnormality of the palmar creases\n- Hypoplastic aortic arch\n- Postaxial polydactyly\n- Biventricular hypertrophy\n- Cleft hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Sinusitis\n- Microcephaly\n- Mastoiditis\n- Malar flattening\n- Epicanthus\n- Long philtrum\n- Micrognathia\n- Small forehead\n- Macrotia\n- Recurrent otitis media\n- Conductive hearing impairment\n- Wide nasal bridge\n- Strabismus\n- Ptosis\n- Single transverse palmar crease\n- Hemangioma\n- Hyperextensibility of the finger joints\n- Global developmental delay\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Prominent ear helix\n- Uplifted earlobe\n- Broad hallux\n- Abnormal shape of the palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Long philtrum\n- Micrognathia\n- Macrotia\n- Recurrent otitis media\n- Wide nasal bridge\n- Astigmatism\n- Optic nerve hypoplasia\n- Atypical behavior\n- Bilateral ptosis\n- Failure to thrive\n- Nasal congestion\n- Splenomegaly\n- Short stature\n- Attention deficit hyperactivity disorder\n- High myopia\n- Recurrent tonsillitis\n- Cutaneous syndactyly\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Micrognathia\n- Low-set ears\n- Macrotia\n- Anteverted nares\n- Cataract\n- Hypotonia\n- Global developmental delay\n- Bilateral ptosis\n- Small for gestational age\n- Craniofacial asymmetry\n- 2-3 toe syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft soft palate\n- Microcephaly\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Wide nose\n- Anteverted nares\n- Ptosis\n- Carious teeth\n- Dental malocclusion\n- Atypical behavior\n- Atrial septal defect\n- Drooling\n- Vertebral fusion\n- Short stature\n- Open bite\n- Diminished mental health\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Epicanthus\n- Microretrognathia\n- Hypertelorism\n- Shallow orbits\n- Bilateral ptosis\n- Broad finger\n- Redundant skin\n- Overlapping toe\n- Poor suck\n- Recurrent upper respiratory tract infections\n- Short nose\n- 2-3 toe syndactyly\n- Capillary hemangioma\n- Feeding difficulties in infancy\n- Infantile muscular hypotonia\n- Short finger\n- Short thumb\n- Underdeveloped supraorbital ridges\n- Broad thumb\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Low-set, posteriorly rotated ears\n- Ptosis\n- Single transverse palmar crease\n- Global developmental delay\n- Failure to thrive\n- Ventricular hypertrophy\n- Ventriculomegaly\n- Achalasia\n- 2-3 toe syndactyly\n- Dysplastic aortic valve\n- Feeding difficulties\n- Nasogastric tube feeding\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Low-set, posteriorly rotated ears\n- Ptosis\n- Single transverse palmar crease\n- Global developmental delay\n- Failure to thrive\n- Ventricular hypertrophy\n- Ventriculomegaly\n- Achalasia\n- 2-3 toe syndactyly\n- Dysplastic aortic valve\n- Feeding difficulties\n- Nasogastric tube feeding\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Micrognathia\n- Posteriorly rotated ears\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Anteverted nares\n- Ptosis\n- Photophobia\n- Autism\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Reduced eye contact\n- Seizure\n- Global developmental delay\n- Generalized hypotonia\n- Failure to thrive\n- Sleep disturbance\n- Decreased facial expression\n- 2-3 toe syndactyly\n- Attention deficit hyperactivity disorder\n- Receptive language delay\n- Feeding difficulties\n- Clinodactyly\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Recurrent otitis media\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Bilateral ptosis\n- Growth delay\n- Elevated hepatic transaminase\n- Short nasal bridge\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Chronic sinusitis\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Bifid uvula\n- Microcephaly\n- Coarse facial features\n- Epicanthus\n- Full cheeks\n- High forehead\n- Bulbous nose\n- Prominent nose\n- Broad nasal tip\n- Delayed puberty\n- Scoliosis\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Thick vermilion border\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Bifid uvula\n- Microcephaly\n- Coarse facial features\n- Epicanthus\n- Full cheeks\n- High forehead\n- Bulbous nose\n- Prominent nose\n- Broad nasal tip\n- Delayed puberty\n- Scoliosis\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Thick vermilion border\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Micropenis\n- Microcephaly\n- Micrognathia\n- Wide nose\n- Anteverted nares\n- Single transverse palmar crease\n- Intellectual disability\n- Global developmental delay\n- Hypertonia\n- Failure to thrive\n- Metatarsus adductus\n- Constipation\n- Pyloric stenosis\n- Intermittent diarrhea\n- Short stature\n- 2-3 toe syndactyly\n- Skin tags\n- 1-2 toe syndactyly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Broad alveolar ridges\n- Microcephaly\n- Epicanthus\n- Micrognathia\n- Posteriorly rotated ears\n- Wide nose\n- Anteverted nares\n- Strabismus\n- Ptosis\n- Sacral dimple\n- Intellectual disability\n- Hypertonia\n- Failure to thrive\n- Metatarsus adductus\n- Episodic vomiting\n- Short stature\n- Abnormality of the palmar creases\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Solitary median maxillary central incisor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/04198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short neck\n- Corneal opacity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/04200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Short philtrum\n- Wide nose\n- Long eyelashes\n- Thick eyebrow\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Clinodactyly of the 5th finger\n- Short stature\n- Depressed nasal bridge\n- Postnatal growth retardation\n- Aplastic\/hypoplastic toenail\n- Camptodactyly\n- Short phalanx of the 5th toe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/04201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Deeply set eye\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Recurrent hypoglycemia\n- Frontal bossing\n- Episodic vomiting\n- Birth length less than 3rd percentile\n- Relative macrocephaly\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Shoulder dimple\n- Prominent forehead\n- Feeding difficulties\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/04202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Deeply set eye\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Recurrent hypoglycemia\n- Frontal bossing\n- Episodic vomiting\n- Birth length less than 3rd percentile\n- Relative macrocephaly\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Shoulder dimple\n- Prominent forehead\n- Feeding difficulties\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/04203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Deeply set eye\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Recurrent hypoglycemia\n- Frontal bossing\n- Episodic vomiting\n- Birth length less than 3rd percentile\n- Relative macrocephaly\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Shoulder dimple\n- Prominent forehead\n- Feeding difficulties\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/04204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Deeply set eye\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Ventricular septal defect\n- Recurrent hypoglycemia\n- Frontal bossing\n- Episodic vomiting\n- Birth length less than 3rd percentile\n- Relative macrocephaly\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Shoulder dimple\n- Prominent forehead\n- Feeding difficulties\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/04205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/04228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Low-set ears\n- Long eyelashes\n- Single transverse palmar crease\n- Hirsutism\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Short middle phalanx of the 5th finger\n- Short stature\n- Coronal craniosynostosis\n- Lacrimal duct stenosis\n- Short middle phalanx of the 3rd finger\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genital system\n- Thick lower lip vermilion\n- Mandibular prognathia\n- Short philtrum\n- Low-set ears\n- Abnormal pinna morphology\n- Overfolded helix\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Gait disturbance\n- Obesity\n- Ventriculomegaly\n- External genital hypoplasia\n- Short stature\n- Tented upper lip vermilion\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypospadias\n- Everted lower lip vermilion\n- Mandibular prognathia\n- High forehead\n- Protruding ear\n- Downslanted palpebral fissures\n- Broad palm\n- Intellectual disability\n- Seizure\n- Short foot\n- Deep philtrum\n- Ventriculomegaly\n- Cavum septum pellucidum\n- Clinodactyly of the 5th finger\n- Short stature\n- Relative macrocephaly\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Widely spaced toes\n- Microtia\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Prominent forehead\n- Bilateral perisylvian polymicrogyria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Long palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Ventriculomegaly\n- Thick nasal alae\n- Wide nasal base\n- Narrow palpebral fissure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Bulbous nose\n- Wide nose\n- Long palpebral fissure\n- Global developmental delay\n- Obesity\n- Thick nasal alae\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Low-set ears\n- Thickened helices\n- Long palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Short foot\n- Metatarsus adductus\n- Short stature\n- Widely spaced toes\n- Thick nasal alae\n- 2-4 toe syndactyly\n- Wide nasal base\n- Narrow palpebral fissure\n- Overfriendliness\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Epicanthus\n- Torticollis\n- Periorbital fullness\n- Hyperpigmentation of the skin\n- Intellectual disability\n- Global developmental delay\n- Joint laxity\n- Short foot\n- Sandal gap\n- Recurrent respiratory infections\n- Cortical dysplasia\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Depressed nasal bridge\n- Knee flexion contracture\n- Attention deficit hyperactivity disorder\n- Microtia\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Prominent supraorbital ridges\n- High forehead\n- Low-set ears\n- Abnormal pinna morphology\n- Strabismus\n- Deeply set eye\n- Upslanted palpebral fissure\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Pes planus\n- Intention tremor\n- Delayed skeletal maturation\n- Short stature\n- Cerebellar vermis atrophy\n- EEG with generalized slow activity\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- High forehead\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Specific learning disability\n- Obesity\n- Pes planus\n- Ventriculomegaly\n- Short stature\n- 2-3 toe syndactyly\n- EEG with generalized slow activity\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micropenis\n- Mandibular prognathia\n- Prominent supraorbital ridges\n- High forehead\n- Cupped ear\n- Thickened helices\n- Bulbous nose\n- Aggressive behavior\n- Intellectual disability\n- Seizure\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Absent speech\n- Short stature\n- Upper limb spasticity\n- Microtia\n- Uplifted earlobe\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Mandibular prognathia\n- Bulbous nose\n- Deeply set eye\n- Aggressive behavior\n- Irritability\n- Hyperactivity\n- Global developmental delay\n- Tremor\n- Short foot\n- Bilateral tonic-clonic seizure\n- Gait imbalance\n- Intellectual disability, moderate\n- Short stature\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Mandibular prognathia\n- Posteriorly rotated ears\n- Hearing impairment\n- Protruding ear\n- Bulbous nose\n- Anteverted nares\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Hypotonia\n- Global developmental delay\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Bilateral cryptorchidism\n- Open bite\n- Protruding tongue\n- Myoclonic absence seizure\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Mandibular prognathia\n- High forehead\n- Abnormal pinna morphology\n- Astigmatism\n- Aggressive behavior\n- Short attention span\n- Irritability\n- Hyperactivity\n- Global developmental delay\n- Talipes equinovarus\n- Gait imbalance\n- Recurrent bronchitis\n- Severe expressive language delay\n- Bilateral cryptorchidism\n- Intellectual disability, severe\n- Myoclonic absence seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Thick lower lip vermilion\n- Long face\n- Pointed chin\n- Thickened helices\n- Protruding ear\n- Atypical behavior\n- Delayed speech and language development\n- Global developmental delay\n- Absent speech\n- Intellectual disability, moderate\n- Short stature\n- Microtia\n- Decreased testicular size\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Short foot\n- Sandal gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gynecomastia\n- Intellectual disability\n- Sandal gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Blindness\n- Phthisis bulbi\n- Intellectual disability\n- Global developmental delay\n- Absent speech\n- Joint hypermobility\n- Small for gestational age\n- Short foot\n- Calcaneovalgus deformity\n- Truncal obesity\n- Apnea\n- Thoracic kyphosis\n- Short stature\n- Decreased testicular size\n- Distal lower limb amyotrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dental crowding\n- obsolete Mood swings\n- Short attention span\n- Hyperactivity\n- Intellectual disability\n- Tremor\n- Hyperreflexia\n- Short foot\n- Truncal obesity\n- Alopecia of scalp\n- Thoracic kyphosis\n- Distal amyotrophy\n- Short stature\n- Hyperextensible hand joints\n- Poor fine motor coordination\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- obsolete Mood swings\n- Short attention span\n- Hyperactivity\n- Intellectual disability\n- Absent speech\n- Joint hypermobility\n- Obesity\n- Short foot\n- Sandal gap\n- Distal amyotrophy\n- Short stature\n- Poor fine motor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- obsolete Mood swings\n- Short attention span\n- Hyperactivity\n- Intellectual disability\n- Absent speech\n- Joint hypermobility\n- Short foot\n- Sandal gap\n- Distal amyotrophy\n- Short stature\n- Poor fine motor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Epicanthus\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Hyperactivity\n- Absent speech\n- Short foot\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Keratosis pilaris\n- Infection-related seizure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Epicanthus\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Hyperactivity\n- Absent speech\n- Short foot\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Keratosis pilaris\n- Infection-related seizure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Hyperactivity\n- Absent speech\n- Short foot\n- Intention tremor\n- Recurrent infections\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Infection-related seizure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thick lower lip vermilion\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Delayed speech and language development\n- Hyperactivity\n- Hyperhidrosis\n- Short foot\n- Intention tremor\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Decreased testicular size\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thick lower lip vermilion\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Delayed speech and language development\n- Hyperactivity\n- Hyperhidrosis\n- Short foot\n- Intention tremor\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Decreased testicular size\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/04327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Thin vermilion border\n- Macrocephaly\n- Short neck\n- Broad neck\n- Upslanted palpebral fissure\n- Synophrys\n- Delayed speech and language development\n- Dry skin\n- Intellectual disability\n- Seizure\n- Obesity\n- Pes planus\n- Short foot\n- Low posterior hairline\n- Generalized hirsutism\n- Downturned corners of mouth\n- Short stature\n- Acute myeloid leukemia\n- Wide intermamillary distance\n- Nail dystrophy\n- Abnormal hair whorl\n- Edema of the dorsum of feet\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Thin vermilion border\n- Macrocephaly\n- Broad face\n- Hypertelorism\n- Short neck\n- Broad neck\n- Upslanted palpebral fissure\n- Synophrys\n- Delayed speech and language development\n- Dry skin\n- Intellectual disability\n- Seizure\n- Pes planus\n- Short foot\n- Low posterior hairline\n- Generalized hirsutism\n- Downturned corners of mouth\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Deep white matter hypodensities\n- Nail dystrophy\n- Abnormal hair whorl\n- Midface retrusion\n- Edema of the dorsum of feet\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Thin vermilion border\n- Broad face\n- Short neck\n- Broad neck\n- Upslanted palpebral fissure\n- Synophrys\n- Delayed speech and language development\n- Dry skin\n- Intellectual disability\n- Seizure\n- Obesity\n- Pes planus\n- Short foot\n- Low posterior hairline\n- Generalized hirsutism\n- Downturned corners of mouth\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Deep white matter hypodensities\n- Abnormal hair whorl\n- Midface retrusion\n- Edema of the dorsum of feet\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Wide mouth\n- Periorbital fullness\n- Periorbital fullness\n- Short nose\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long philtrum\n- Bulbous nose\n- Anteverted nares\n- Abnormal heart morphology\n- Respiratory distress\n- Supravalvular aortic stenosis\n- Thick vermilion border\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad forehead\n- Bulbous nose\n- Periorbital fullness\n- Anxiety\n- Delayed speech and language development\n- Enuresis\n- Soft skin\n- Global developmental delay\n- Downturned corners of mouth\n- Depressed nasal bridge\n- Attention deficit hyperactivity disorder\n- Prematurely aged appearance\n- Thick vermilion border\n- Overfriendliness\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Bulbous nose\n- Periorbital fullness\n- Delayed speech and language development\n- Enuresis\n- Global developmental delay\n- Depressed nasal bridge\n- Impaired visuospatial constructive cognition\n- Overfriendliness\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Global developmental delay\n- Pituitary microadenoma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Atypical behavior\n- Hypothyroidism\n- Cyanosis\n- Global developmental delay\n- Radioulnar synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Hypertelorism\n- Underdeveloped nasal alae\n- Short neck\n- Broad neck\n- Upslanted palpebral fissure\n- Synophrys\n- Dry skin\n- Seizure\n- Pes planus\n- Short foot\n- Low posterior hairline\n- Generalized hirsutism\n- Difficulty walking\n- Hyperbilirubinemia\n- Short stature\n- Preauricular pit\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Nail dystrophy\n- Proximal placement of thumb\n- Low hanging columella\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Chronic constipation\n- Recurrent cutaneous abscess formation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Recurrent otitis media\n- Underdeveloped nasal alae\n- Upslanted palpebral fissure\n- Synophrys\n- Dry skin\n- Pes cavus\n- Short foot\n- Recurrent respiratory infections\n- Generalized hirsutism\n- Intellectual disability, moderate\n- Low hanging columella\n- Chronic constipation\n- Pineal cyst\n- Joint subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Hearing impairment\n- Underdeveloped nasal alae\n- Short neck\n- Broad neck\n- Upslanted palpebral fissure\n- Synophrys\n- Dry skin\n- Seizure\n- Pes cavus\n- Short foot\n- Low posterior hairline\n- Generalized hirsutism\n- Depressed nasal bridge\n- Proximal placement of thumb\n- Low hanging columella\n- Intellectual disability, severe\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Hypertelorism\n- Underdeveloped nasal alae\n- Short neck\n- Broad neck\n- Synophrys\n- Spasticity\n- Ventricular septal defect\n- Mitral stenosis\n- Double outlet right ventricle\n- Bilateral tonic-clonic seizure\n- Pulmonary arterial hypertension\n- Global brain atrophy\n- Motor deterioration\n- Abnormal cortical gyration\n- Depressed nasal bridge\n- Persistent left superior vena cava\n- Wide intermamillary distance\n- Proximal placement of thumb\n- Low hanging columella\n- Intellectual disability, severe\n- Supratentorial neoplasm\n- Clubbing of toes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Underdeveloped nasal alae\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Bilateral talipes equinovarus\n- Neutropenia\n- Low posterior hairline\n- Abnormal cerebral white matter morphology\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Low hanging columella\n- Intellectual disability, severe\n- Myoclonic absence seizure\n- Respiratory tract infection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/04374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/04375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/04376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/04377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Long philtrum\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Bilateral talipes equinovarus\n- Scoliosis\n- Kyphosis\n- Knee dislocation\n- Bilateral elbow dislocations\n- Depressed nasal bridge\n- Supernumerary metacarpal bones\n- Abnormality of the palmar creases\n- Broad fingertip\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Long philtrum\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Bilateral talipes equinovarus\n- Scoliosis\n- Kyphosis\n- Knee dislocation\n- Bilateral elbow dislocations\n- Depressed nasal bridge\n- Supernumerary metacarpal bones\n- Abnormality of the palmar creases\n- Broad fingertip\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Anteverted nares\n- Pectus excavatum\n- Arachnodactyly\n- Slender finger\n- Hallux valgus\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Spastic tetraparesis\n- Myelopathy\n- Motor deterioration\n- Kyphosis\n- Shoulder dislocation\n- Depressed nasal bridge\n- Hyperactive deep tendon reflexes\n- Vertebral wedging\n- Prominent forehead\n- Neck pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Hypertelorism\n- Facial asymmetry\n- High forehead\n- Myopia\n- Hypodontia\n- Dental malocclusion\n- Periodontitis\n- Spatulate thumbs\n- Abnormal spinal cord morphology\n- Hip dislocation\n- Short stature\n- Knee dislocation\n- Depressed nasal bridge\n- Shortening of all metacarpals\n- Prominent forehead\n- Midface retrusion\n- Long fingers\n- Frontal open bite\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Talipes equinovarus\n- Genu recurvatum\n- Hip dislocation\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Recurrent upper respiratory tract infections\n- Depressed nasal bridge\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Broad forehead\n- Talipes equinovarus\n- Talipes equinovalgus\n- Hip dislocation\n- Depressed nasal bridge\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Wide nasal bridge\n- Joint dislocation\n- Short nail\n- Short toe\n- Hip dislocation\n- Fibular hypoplasia\n- Elbow dislocation\n- Short palm\n- Knee dislocation\n- Depressed nasal bridge\n- Multiple palmar creases\n- Pes valgus\n- Short metacarpal\n- Short metatarsal\n- Concave nasal ridge\n- Broad thumb\n- Flat face\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Nystagmus\n- Abnormality of the skin\n- Abnormal thumb morphology\n- Slender finger\n- Intellectual disability, mild\n- Joint hypermobility\n- Disproportionate tall stature\n- Pes planus\n- Kyphoscoliosis\n- Abnormality of the wrist\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/04388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Nystagmus\n- Abnormality of the skin\n- Abnormal thumb morphology\n- Slender finger\n- Intellectual disability, mild\n- Joint hypermobility\n- Disproportionate tall stature\n- Pes planus\n- Kyphoscoliosis\n- Abnormality of the wrist\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/04389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Strabismus\n- Abnormal sternum morphology\n- Abnormal thumb morphology\n- Slender finger\n- Intellectual disability, mild\n- Joint hypermobility\n- Disproportionate tall stature\n- Kyphoscoliosis\n- Cerebellar vermis atrophy\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/04390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Strabismus\n- Autistic behavior\n- Abnormal sternum morphology\n- Slender finger\n- Seizure\n- Limited elbow extension\n- Disproportionate tall stature\n- Abnormal mitral valve morphology\n- Cerebral cortical atrophy\n- Intellectual disability, moderate\n- Kyphoscoliosis\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/04391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/04416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/04417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Delayed cranial suture closure\n- Brachydactyly\n- Growth delay\n- Gastroesophageal reflux\n- Abnormal renal morphology\n- Wide nasal base\n- Clinodactyly\n- Hooded eyelid\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the vertebral column\n- Brachydactyly\n- Intellectual disability\n- Gastroesophageal reflux\n- Postnatal growth retardation\n- Clinodactyly\n- Abnormality of limbs\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachydactyly\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Postnatal growth retardation\n- Clinodactyly\n- Abnormality of limbs\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachydactyly\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Postnatal growth retardation\n- Clinodactyly\n- Abnormality of limbs\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Myopia\n- Intrauterine growth retardation\n- Atrial septal defect\n- Coarctation of aorta\n- Accessory spleen\n- Gastroesophageal reflux\n- Supernumerary ribs\n- Severe sensorineural hearing impairment\n- Intellectual disability, severe\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Sensorineural hearing impairment\n- Ptosis\n- Myopia\n- Intellectual disability, mild\n- Talipes equinovarus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macrocephaly\n- Myopia\n- Intrauterine growth retardation\n- Pulmonic stenosis\n- Short foot\n- Clinodactyly of the 5th finger\n- Fetal pyelectasis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macrocephaly\n- Myopia\n- Intrauterine growth retardation\n- Pulmonic stenosis\n- Short foot\n- Clinodactyly of the 5th finger\n- Fetal pyelectasis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Dental malocclusion\n- Seizure\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Dental malocclusion\n- Seizure\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Ptosis\n- Myopia\n- Microdontia\n- Autistic behavior\n- Short ribs\n- Brachydactyly\n- Intrauterine growth retardation\n- Short foot\n- Short toe\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Lacrimal duct stenosis\n- Proximal placement of thumb\n- Short thumb\n- Tooth agenesis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Ptosis\n- Myopia\n- Microdontia\n- Autistic behavior\n- Short ribs\n- Brachydactyly\n- Intrauterine growth retardation\n- Short foot\n- Short toe\n- Gastroesophageal reflux\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Lacrimal duct stenosis\n- Proximal placement of thumb\n- Short thumb\n- Tooth agenesis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Low anterior hairline\n- Hypertelorism\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Upslanted palpebral fissure\n- Synophrys\n- Widely spaced teeth\n- Aggressive behavior\n- Hypotonia\n- Absent speech\n- Flexion contracture\n- Hypoplasia of the corpus callosum\n- Spastic tetraplegia\n- Scoliosis\n- Short middle phalanx of the 5th finger\n- Depressed nasal bridge\n- Bilateral sensorineural hearing impairment\n- Short 4th metacarpal\n- Broad columella\n- Primary microcephaly\n- Midface retrusion\n- Feeding difficulties\n- Clinodactyly\n- Narrow palpebral fissure\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Short philtrum\n- Wide nasal bridge\n- Strabismus\n- Widely spaced teeth\n- Inappropriate laughter\n- Seizure\n- Hypotonia\n- Thrombocytopenia\n- Intestinal malrotation\n- Downturned corners of mouth\n- Hypoplastic philtrum\n- Primary microcephaly\n- Hypopituitarism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Short philtrum\n- Wide nasal bridge\n- Strabismus\n- Widely spaced teeth\n- Inappropriate laughter\n- Seizure\n- Hypotonia\n- Thrombocytopenia\n- Intestinal malrotation\n- Downturned corners of mouth\n- Hypoplastic philtrum\n- Primary microcephaly\n- Hypopituitarism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Pointed chin\n- Short philtrum\n- Hearing impairment\n- Bulbous nose\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Hyperactivity\n- Cerebellar atrophy\n- Absent speech\n- Broad finger\n- Short toe\n- Vomiting\n- Sleep disturbance\n- Axial hypotonia\n- Short finger\n- Uplifted earlobe\n- Chronic constipation\n- Alternating exotropia\n- Near esotropia\n- Esophagitis\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Thin vermilion border\n- Smooth philtrum\n- Micrognathia\n- High forehead\n- Low-set ears\n- Sensorineural hearing impairment\n- Prominent nasal bridge\n- Wide nasal bridge\n- Retinal coloboma\n- Microphthalmia\n- Coloboma\n- Optic nerve hypoplasia\n- Peters anomaly\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Abnormal cerebellum morphology\n- Absent speech\n- Abnormal heart morphology\n- Ventricular septal defect\n- Patent foramen ovale\n- Hypoplasia of the corpus callosum\n- Hypoplasia of the brainstem\n- Downturned corners of mouth\n- Cleft ala nasi\n- Secondary microcephaly\n- Wide intermamillary distance\n- Lateral ventricle dilatation\n- Abnormality of the palmar creases\n- Prominent forehead\n- Cerebral white matter hypoplasia\n- Enlarged thalamic volume\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Short philtrum\n- Low-set ears\n- Thickened helices\n- Sensorineural hearing impairment\n- Prominent nasal bridge\n- Retinal coloboma\n- Ptosis\n- Long eyelashes\n- Microphthalmia\n- Coloboma\n- Iris coloboma\n- Single transverse palmar crease\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Abnormal cerebellum morphology\n- Cerebellar hypoplasia\n- Absent speech\n- Abnormal heart morphology\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Hypoplasia of the corpus callosum\n- Hypoplasia of the brainstem\n- Downturned corners of mouth\n- Tricuspid regurgitation\n- Secondary microcephaly\n- Pericallosal lipoma\n- Prominent ear helix\n- Prominent forehead\n- Cerebral white matter hypoplasia\n- Enlarged thalamic volume\n- Subcortical heterotopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Smooth philtrum\n- Prominent nasal bridge\n- Prominent nose\n- Retinal coloboma\n- Coloboma\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Abnormal cerebellum morphology\n- Cerebellar hypoplasia\n- Absent speech\n- Hypoplasia of the corpus callosum\n- Downturned corners of mouth\n- Enlarged posterior fossa\n- Secondary microcephaly\n- Lateral ventricle dilatation\n- Ectropion of lower eyelids\n- Abnormality of the palmar creases\n- Prominent forehead\n- Cerebral white matter hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Macroglossia\n- Narrow palate\n- Bifid uvula\n- High palate\n- Dolichocephaly\n- Long face\n- Hearing impairment\n- Underdeveloped nasal alae\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Long palpebral fissure\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Ventricular septal defect\n- Pes planus\n- Abnormal hallux morphology\n- Constipation\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Vertebral segmentation defect\n- Short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Prominent metopic ridge\n- Wide intermamillary distance\n- Impaired pain sensation\n- Broad lateral eyebrow\n- Pes valgus\n- Six lumbar vertebrae\n- Hypoplastic helices\n- Open bite\n- Agenesis of molar\n- Wide nasal ridge\n- Abnormality of the plantar skin of foot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Macroglossia\n- Narrow palate\n- Bifid uvula\n- High palate\n- Dolichocephaly\n- Long face\n- Hearing impairment\n- Underdeveloped nasal alae\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Long palpebral fissure\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Ventricular septal defect\n- Pes planus\n- Abnormal hallux morphology\n- Constipation\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Vertebral segmentation defect\n- Short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Prominent metopic ridge\n- Wide intermamillary distance\n- Impaired pain sensation\n- Broad lateral eyebrow\n- Pes valgus\n- Six lumbar vertebrae\n- Hypoplastic helices\n- Open bite\n- Agenesis of molar\n- Wide nasal ridge\n- Abnormality of the plantar skin of foot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Macroglossia\n- Narrow palate\n- Bifid uvula\n- High palate\n- Dolichocephaly\n- Long face\n- Hearing impairment\n- Underdeveloped nasal alae\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Long palpebral fissure\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Ventricular septal defect\n- Pes planus\n- Abnormal hallux morphology\n- Constipation\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Vertebral segmentation defect\n- Short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Prominent metopic ridge\n- Wide intermamillary distance\n- Impaired pain sensation\n- Broad lateral eyebrow\n- Pes valgus\n- Six lumbar vertebrae\n- Hypoplastic helices\n- Open bite\n- Agenesis of molar\n- Wide nasal ridge\n- Abnormality of the plantar skin of foot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Wide mouth\n- High palate\n- Microcephaly\n- Broad philtrum\n- Full cheeks\n- Hypomimic face\n- Narrow forehead\n- Low-set ears\n- Macrotia\n- Abnormal nasal bridge morphology\n- Prominent nasal bridge\n- Downslanted palpebral fissures\n- Hypermetropia\n- Long palpebral fissure\n- Delayed speech and language development\n- Single transverse palmar crease\n- Spasticity\n- Global developmental delay\n- Hip dysplasia\n- Failure to thrive\n- Overlapping toe\n- Deep philtrum\n- Low posterior hairline\n- Tetraparesis\n- Skeletal muscle atrophy\n- Short stature\n- Decreased body weight\n- Atrioventricular canal defect\n- Demyelinating peripheral neuropathy\n- Equinovarus deformity\n- Proximal placement of thumb\n- Open bite\n- Intellectual disability, severe\n- Wide nasal ridge\n- Systolic heart murmur\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/04458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Cataract\n- Osteoporosis\n- Penetrating foot ulcers\n- Poikiloderma\n- Poor wound healing\n- Limitation of joint mobility\n- Alopecia\n- Hallux valgus\n- Osteoarthritis\n- External genital hypoplasia\n- Reduced subcutaneous adipose tissue\n- Dermal atrophy\n- Type II diabetes mellitus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Absent eyelashes\n- Cutaneous photosensitivity\n- Poikiloderma\n- Growth delay\n- Diarrhea\n- Plantar hyperkeratosis\n- Sparse hair\n- Nail dystrophy\n- Increased bone mineral density\n- Food intolerance\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Sparse eyelashes\n- Abnormal dental enamel morphology\n- Insulin resistance\n- Osteopenia\n- Growth delay\n- Anemia\n- Diarrhea\n- Fine hair\n- Hypercholesterolemia\n- Increased circulating ferritin concentration\n- Short stature\n- Alveolar rhabdomyosarcoma\n- Plantar hyperkeratosis\n- Sparse hair\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormality of the genitourinary system\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Short philtrum\n- Abnormal pinna morphology\n- Anteverted nares\n- Deeply set eye\n- Upslanted palpebral fissure\n- Atypical behavior\n- Single transverse palmar crease\n- Brachydactyly\n- Broad palm\n- Seizure\n- Hypotonia\n- Absent speech\n- Sandal gap\n- Frontal upsweep of hair\n- Short nose\n- Clinodactyly of the 5th finger\n- Depigmentation\/hyperpigmentation of skin\n- Microtia\n- Large earlobe\n- Intellectual disability, severe\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/04462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Hypertelorism\n- Anteverted nares\n- Upslanted palpebral fissure\n- Hypotonia\n- Short nose\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Midface retrusion\n- Feeding difficulties\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/04463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Abnormality of the dentition\n- Brachycephaly\n- Coarse facial features\n- Low anterior hairline\n- Pointed chin\n- Hypertelorism\n- Abnormal pinna morphology\n- Anteverted nares\n- Synophrys\n- Atypical behavior\n- Broad palm\n- Seizure\n- Hypotonia\n- Obesity\n- Large for gestational age\n- Broad foot\n- Short foot\n- Bilateral talipes equinovarus\n- Short nose\n- Short palm\n- Increased body weight\n- Horizontal eyebrow\n- Midface retrusion\n- Skin-picking\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/04464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Coarse facial features\n- Pointed chin\n- Hypertelorism\n- Abnormal pinna morphology\n- Upslanted palpebral fissure\n- Single transverse palmar crease\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Abnormal heart morphology\n- Short stature\n- Depigmentation\/hyperpigmentation of skin\n- Feeding difficulties in infancy\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/04465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Pointed chin\n- Synophrys\n- Atypical behavior\n- Brachydactyly\n- Hypotonia\n- Obesity\n- Sleep disturbance\n- Short palm\n- Depigmentation\/hyperpigmentation of skin\n- U-Shaped upper lip vermilion\n- Intellectual disability, severe\n- Midface retrusion\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/04466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/04478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormality of the dentition\n- Brachycephaly\n- Round face\n- Hypertelorism\n- Bulbous nose\n- Prominent nasal bridge\n- Anteverted nares\n- Deeply set eye\n- Synophrys\n- Dental crowding\n- Atypical behavior\n- Autistic behavior\n- Hyperactivity\n- Tapered finger\n- Seizure\n- Abnormal facial shape\n- Low posterior hairline\n- Coarse hair\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Abnormal hand morphology\n- Attention deficit hyperactivity disorder\n- Short 5th finger\n- Incisor macrodontia\n- Talon cusp\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Hearing impairment\n- Autistic behavior\n- Abnormality of the hand\n- Brachydactyly\n- Seizure\n- Intellectual disability, mild\n- Abnormal facial shape\n- Intellectual disability, moderate\n- Bilateral conductive hearing impairment\n- Bilateral sensorineural hearing impairment\n- Abnormality of premolar\n- Incisor macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormality of the dentition\n- Abnormal palate morphology\n- Brachycephaly\n- Abnormality of the face\n- Round face\n- Hypertelorism\n- Hearing impairment\n- Bulbous nose\n- Prominent nasal bridge\n- Strabismus\n- Hypermetropia\n- Autistic behavior\n- Hyperactivity\n- Abnormality of the hand\n- Brachydactyly\n- Tapered finger\n- Intellectual disability, mild\n- Low posterior hairline\n- Coarse hair\n- Intellectual disability, moderate\n- Clinodactyly of the 5th finger\n- Short stature\n- Bilateral conductive hearing impairment\n- Incisor macrodontia\n- Talon cusp\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Abnormality of the face\n- Long philtrum\n- Hearing impairment\n- Prominent nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Autistic behavior\n- Abnormal rib morphology\n- Abnormality of the vertebral column\n- Abnormality of the hand\n- Intellectual disability, mild\n- Scoliosis\n- Short stature\n- Incisor macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Bulbous nose\n- Wide nasal bridge\n- Anteverted nares\n- Deeply set eye\n- Atypical behavior\n- Aggressive behavior\n- Inflexible adherence to routines or rituals\n- Impaired social interactions\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Slurred speech\n- Intrauterine growth retardation\n- Polyhydramnios\n- Coarse hair\n- Recurrent upper respiratory tract infections\n- Clinodactyly of the 5th finger\n- Short stature\n- Poor fine motor coordination\n- Enuresis nocturna\n- Incisor macrodontia\n- Talon cusp\n- Chronic sinusitis\n- Abnormal social behavior\n- Wheezing\n- Impaired toileting ability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Protruding ear\n- Bulbous nose\n- Prominent nasal bridge\n- Anteverted nares\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Single transverse palmar crease\n- Brachydactyly\n- Intellectual disability, mild\n- Intrauterine growth retardation\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Attention deficit hyperactivity disorder\n- Short 5th finger\n- Incisor macrodontia\n- Caesarian section\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal palate morphology\n- Velopharyngeal insufficiency\n- Thin vermilion border\n- Retrognathia\n- Stapes ankylosis\n- Stenosis of the external auditory canal\n- Conductive hearing impairment\n- Bulbous nose\n- Prominent nasal bridge\n- Synophrys\n- Autistic behavior\n- Impaired social interactions\n- Anxiety\n- Global developmental delay\n- Intrauterine growth retardation\n- Hypernasal speech\n- Abnormal heart morphology\n- Ventricular septal defect\n- Recurrent upper respiratory tract infections\n- Clinodactyly of the 5th finger\n- Avascular necrosis of the capital femoral epiphysis\n- Bilateral single transverse palmar creases\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Round face\n- Long philtrum\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Thickened nuchal skin fold\n- Cervical ribs\n- Exaggerated cupid's bow\n- Delayed skeletal maturation\n- Short stature\n- Prominent nasal tip\n- Avascular necrosis of the capital femoral epiphysis\n- Mild global developmental delay\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Round face\n- Long philtrum\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Thickened nuchal skin fold\n- Cervical ribs\n- Exaggerated cupid's bow\n- Delayed skeletal maturation\n- Short stature\n- Prominent nasal tip\n- Avascular necrosis of the capital femoral epiphysis\n- Mild global developmental delay\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Long philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Synophrys\n- Compulsive behaviors\n- Intellectual disability\n- Intellectual disability, moderate\n- Lumbar hyperlordosis\n- Abnormal vertebral morphology\n- Short stature\n- Poor fine motor coordination\n- Short 5th metacarpal\n- Delayed fine motor development\n- Incisor macrodontia\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Turricephaly\n- Round face\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Autistic behavior\n- Intellectual disability, mild\n- Motor delay\n- Ventricular septal defect\n- Generalized non-motor (absence) seizure\n- Short stature\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- Incisor macrodontia\n- Wide nasal base\n- Preeclampsia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Turricephaly\n- Round face\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Autistic behavior\n- Intellectual disability, mild\n- Motor delay\n- Ventricular septal defect\n- Generalized non-motor (absence) seizure\n- Short stature\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- Incisor macrodontia\n- Wide nasal base\n- Preeclampsia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Long philtrum\n- Prominent nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Sparse eyelashes\n- Hyperactivity\n- Specific learning disability\n- Hip dysplasia\n- Low posterior hairline\n- Coarse hair\n- Clinodactyly of the 5th finger\n- Incisor macrodontia\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Brachycephaly\n- Microcephaly\n- Bulbous nose\n- Anxiety\n- Seizure\n- Intellectual disability, mild\n- Motor delay\n- Umbilical hernia\n- Scoliosis\n- Short stature\n- Atrioventricular canal defect\n- Abnormal distal phalanx morphology of finger\n- Incisor macrodontia\n- Wide nasal base\n- Panic attack\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Brachycephaly\n- Microcephaly\n- Bulbous nose\n- Anxiety\n- Seizure\n- Intellectual disability, mild\n- Motor delay\n- Umbilical hernia\n- Scoliosis\n- Short stature\n- Atrioventricular canal defect\n- Abnormal distal phalanx morphology of finger\n- Incisor macrodontia\n- Wide nasal base\n- Panic attack\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Brachycephaly\n- Microcephaly\n- Bulbous nose\n- Anxiety\n- Seizure\n- Intellectual disability, mild\n- Motor delay\n- Umbilical hernia\n- Scoliosis\n- Short stature\n- Atrioventricular canal defect\n- Abnormal distal phalanx morphology of finger\n- Incisor macrodontia\n- Wide nasal base\n- Panic attack\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Protruding ear\n- Thick eyebrow\n- Synophrys\n- Dental crowding\n- Aggressive behavior\n- Restrictive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Delayed speech and language development\n- Pectus excavatum\n- Low posterior hairline\n- Poor speech\n- Expressive language delay\n- Short stature\n- Preauricular pit\n- Attention deficit hyperactivity disorder\n- Hypoplastic helices\n- Abnormal incisor morphology\n- Incisor macrodontia\n- Wide nasal base\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anteverted nares\n- Upslanted palpebral fissure\n- Synophrys\n- Abnormal dental enamel morphology\n- Single transverse palmar crease\n- Brachydactyly\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Obesity\n- Lumbar hyperlordosis\n- Short stature\n- Short humerus\n- Bilateral conductive hearing impairment\n- Incisor macrodontia\n- Prominent eyelashes\n- Midface retrusion\n- Pineal cyst\n- Wide nasal base\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Delayed cranial suture closure\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Thickened helices\n- Astigmatism\n- Long eyelashes\n- Autistic behavior\n- Inflexible adherence to routines or rituals\n- Impaired social interactions\n- Broad palm\n- Intellectual disability, mild\n- Motor delay\n- Bilateral ptosis\n- Polyhydramnios\n- Hypernasal speech\n- Ventriculomegaly\n- Low posterior hairline\n- Memory impairment\n- Expressive language delay\n- Delayed skeletal maturation\n- Inverted nipples\n- Disproportionate short stature\n- Short stature\n- Abnormal dental pulp morphology\n- Dyslexia\n- Incisor macrodontia\n- Abnormal optic disc morphology\n- Frequent temper tantrums\n- Tics\n- Periauricular skin pits\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal palate morphology\n- Retrognathia\n- Hearing impairment\n- Low-set ears\n- Bulbous nose\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Sacral dimple\n- Atypical scarring of skin\n- Brachydactyly\n- Intellectual disability, mild\n- Global developmental delay\n- Small for gestational age\n- Hypernasal speech\n- Small nail\n- Polycythemia\n- Hypoglycemia\n- Intellectual disability, moderate\n- Delayed skeletal maturation\n- Multiple joint contractures\n- Arthralgia\n- Spinal rigidity\n- Clinodactyly of the 5th finger\n- Finger joint hypermobility\n- Dysplastic corpus callosum\n- Attention deficit hyperactivity disorder\n- Contracture of the distal interphalangeal joint of the 5th finger\n- Contracture of the distal interphalangeal joint of the 4th finger\n- Contracture of the distal interphalangeal joint of the 3rd finger\n- Contracture of the distal interphalangeal joint of the 2nd finger\n- Short distal phalanx of finger\n- Short hallux\n- Osteochondritis dissecans\n- Incisor macrodontia\n- Bone fracture\n- Stiff finger\n- Stiff hip\n- Testicular torsion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Triangular face\n- Long philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Ptosis\n- Myopia\n- Widely-spaced maxillary central incisors\n- Premature birth\n- Abnormal facial shape\n- Intellectual disability, moderate\n- Cervical kyphosis\n- Short stature\n- Short 5th finger\n- Incisor macrodontia\n- Broad eyebrow\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- Prominent nasal bridge\n- Anteverted nares\n- Myopia\n- Thick eyebrow\n- Seizure\n- Specific learning disability\n- Intellectual disability, moderate\n- Cervical kyphosis\n- Short stature\n- Premature loss of teeth\n- Short 5th finger\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/04507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Cupped ear\n- Wide nasal bridge\n- Ptosis\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability, mild\n- Global developmental delay\n- Small nail\n- Intellectual disability, moderate\n- Short stature\n- Polysyndactyly of hallux\n- Congenital bilateral ptosis\n- Hypoplastic helices\n- Short 5th finger\n- Overweight\n- Clinodactyly\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/04508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Coarse facial features\n- Deeply set eye\n- Hypotelorism\n- Osteopenia\n- Soft skin\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Photosensitive myoclonic seizure\n- Failure to thrive\n- Short foot\n- Gait ataxia\n- Broad-based gait\n- Unsteady gait\n- Sleep disturbance\n- Highly arched eyebrow\n- Polyphagia\n- Prominent nasal tip\n- Sparse hair\n- Tapered toe\n- Short digit\n- Feeding difficulties\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/04509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Smooth philtrum\n- Anxiety\n- Prominent fingertip pads\n- Global developmental delay\n- Obesity\n- Highly arched eyebrow\n- Short palm\n- Increased body weight\n- Deep palmar crease\n- Low hanging columella\n- Nasal regurgitation\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/04510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Microretrognathia\n- High forehead\n- Bulbous nose\n- Underdeveloped nasal alae\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Brachydactyly\n- Motor delay\n- Plagiocephaly\n- Joint laxity\n- Obesity\n- Broad foot\n- Thin nail\n- Poor suck\n- Short nose\n- Short middle phalanx of the 5th finger\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Axial hypotonia\n- Short middle phalanx of the 2nd finger\n- Broad hallux\n- Abnormality of pain sensation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/04511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Thin vermilion border\n- Epicanthus\n- Prominent nasal bridge\n- Strabismus\n- Upslanted palpebral fissure\n- Tapered finger\n- Slender finger\n- Seizure\n- Global developmental delay\n- Plagiocephaly\n- Joint laxity\n- Pes planus\n- Sandal gap\n- Recurrent upper respiratory tract infections\n- Clinodactyly of the 5th finger\n- Attention deficit hyperactivity disorder\n- Attached earlobe\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/04512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Posteriorly rotated ears\n- Anteverted nares\n- Cataract\n- Synophrys\n- Eczema\n- Brachydactyly\n- Intellectual disability\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Constipation\n- Highly arched eyebrow\n- Obstructive sleep apnea\n- Severe short stature\n- Decreased body weight\n- Lumbar kyphoscoliosis\n- Hypoplasia of proximal radius\n- Hypoplasia of proximal fibula\n- Chronic lung disease\n- Thickened ears\n- Grade I vesicoureteral reflux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/04530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/04537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/04567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/04572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/04573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/04574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/04575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/04576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/04577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/04578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/04584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/04585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/04586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/04587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/04588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/04589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/04590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/04591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/04592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/04593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/04602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Broad forehead\n- Long philtrum\n- Hearing impairment\n- Wide nose\n- Ptosis\n- Hypertension\n- Seizure\n- Hypotonia\n- Motor delay\n- Agenesis of corpus callosum\n- Right ventricular hypertrophy\n- Right ventricular failure\n- Dysphagia\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Curved fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/04616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Long philtrum\n- Anteverted nares\n- Proptosis\n- Abnormal repetitive mannerisms\n- Short attention span\n- Anxiety\n- Delayed speech and language development\n- Decreased response to growth hormone stimulation test\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Hip dysplasia\n- Dysphagia\n- Sleep disturbance\n- Short nose\n- Somatic sensory dysfunction\n- Short stature\n- Attention deficit hyperactivity disorder\n- Tented upper lip vermilion\n- Delayed fine motor development\n- Feeding difficulties\n- Skin-picking\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/04617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin vermilion border\n- Broad philtrum\n- Long philtrum\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Reduced eye contact\n- Global developmental delay\n- Absent speech\n- Hip dysplasia\n- Abnormality of the cardiovascular system\n- Gastroesophageal reflux\n- Incoordination\n- Sleep disturbance\n- Intellectual disability, severe\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/04618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin vermilion border\n- Broad philtrum\n- Long philtrum\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Reduced eye contact\n- Global developmental delay\n- Absent speech\n- Hip dysplasia\n- Abnormality of the cardiovascular system\n- Gastroesophageal reflux\n- Incoordination\n- Sleep disturbance\n- Intellectual disability, severe\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/04619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/04620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/04621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/04622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/04623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/04624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/04643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/04674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/04677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/04680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/04681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/04682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/04683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/04684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Wide nasal bridge\n- Broad nasal tip\n- Astigmatism\n- Dementia\n- Anxiety\n- Reduced eye contact\n- Rheumatoid arthritis\n- Macrodontia\n- Nail pits\n- Dysphagia\n- Migraine\n- Kyphosis\n- Scapular winging\n- Short stature\n- Attention deficit hyperactivity disorder\n- Short finger\n- Dyslexia\n- Mild global developmental delay\n- Mild expressive language delay\n- Feeding difficulties\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/04685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/04694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Anteverted nares\n- Hyperactivity\n- Hirsutism\n- Seizure\n- Growth delay\n- EEG abnormality\n- Highly arched eyebrow\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Anteverted nares\n- Hyperactivity\n- Hirsutism\n- Seizure\n- Growth delay\n- EEG abnormality\n- Highly arched eyebrow\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Anteverted nares\n- Hyperactivity\n- Hirsutism\n- Seizure\n- Growth delay\n- EEG abnormality\n- Highly arched eyebrow\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Anteverted nares\n- Hyperactivity\n- Hirsutism\n- Seizure\n- Growth delay\n- EEG abnormality\n- Highly arched eyebrow\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/04698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Disproportionate tall stature\n- Scoliosis\n- Intellectual disability, severe\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/04699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n- Narrow foot\n- Gait imbalance\n- Recurrent infections\n- Narrow palm\n- Intellectual disability, severe\n- Cerebral palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/04700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cutis laxa\n- Intellectual disability\n- Hypotonia\n- Obesity\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/04701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/04702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/04703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/04704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/04705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/04706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/04707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/04708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/04709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/04710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/04711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/04712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/04713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/04714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/04715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/04716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/04717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/04718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Hypertelorism\n- Anteverted nares\n- Cerebellar vermis hypoplasia\n- Abnormal heart morphology\n- Bilateral cleft lip and palate\n- Abnormal respiratory system physiology\n- Laryngeal cleft\n- Mild global developmental delay\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Hypertelorism\n- Anteverted nares\n- Cerebellar vermis hypoplasia\n- Abnormal heart morphology\n- Bilateral cleft lip and palate\n- Abnormal respiratory system physiology\n- Laryngeal cleft\n- Mild global developmental delay\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Hypertelorism\n- Anteverted nares\n- Abnormal heart morphology\n- Bilateral cleft lip and palate\n- Abnormal respiratory system physiology\n- Laryngeal cleft\n- Mild global developmental delay\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/04732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Hypertelorism\n- Widow's peak\n- Wide nasal bridge\n- Broad nasal tip\n- Delayed speech and language development\n- Global developmental delay\n- Omphalocele\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- Recurrent infections\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/04733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocele testis\n- Shawl scrotum\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Ptosis\n- Dental crowding\n- Abnormal dental enamel morphology\n- Natal tooth\n- Single umbilical artery\n- Global developmental delay\n- Abnormal umbilicus morphology\n- Ventricular septal defect\n- Aortic root aneurysm\n- Coronal craniosynostosis\n- Sagittal craniosynostosis\n- Preauricular pit\n- Six lumbar vertebrae\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/04734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocele testis\n- Shawl scrotum\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Ptosis\n- Dental crowding\n- Abnormal dental enamel morphology\n- Natal tooth\n- Single umbilical artery\n- Global developmental delay\n- Abnormal umbilicus morphology\n- Ventricular septal defect\n- Aortic root aneurysm\n- Coronal craniosynostosis\n- Sagittal craniosynostosis\n- Preauricular pit\n- Six lumbar vertebrae\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/04735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Ptosis\n- Bicornuate uterus\n- Short stature\n- Preauricular pit\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/04736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/04748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/04749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/04750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/04751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/04752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/04779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/04780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/04781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/04782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/04783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Aggressive behavior\n- Global developmental delay\n- Recurrent hand flapping\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/04784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/04806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/04807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/04826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Intrauterine growth retardation\n- Bilateral talipes equinovarus\n- Scoliosis\n- Delayed skeletal maturation\n- Elbow dislocation\n- Knee dislocation\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Bilateral talipes equinovarus\n- Hip dislocation\n- Knee dislocation\n- Depressed nasal bridge\n- Supernumerary metacarpal bones\n- Broad hallux\n- Prominent forehead\n- Broad fingertip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Telecanthus\n- Joint laxity\n- Intrauterine growth retardation\n- Bilateral talipes equinovarus\n- Delayed skeletal maturation\n- Knee dislocation\n- Bilateral elbow dislocations\n- Depressed nasal bridge\n- Prominent forehead\n- Broad fingertip\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Talipes equinovarus\n- Scoliosis\n- Hip dislocation\n- Elbow dislocation\n- Short stature\n- Knee dislocation\n- Depressed nasal bridge\n- Supernumerary metacarpal bones\n- Prominent forehead\n- Broad fingertip\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Talipes equinovarus\n- Scoliosis\n- Hip dislocation\n- Elbow dislocation\n- Short stature\n- Knee dislocation\n- Depressed nasal bridge\n- Supernumerary metacarpal bones\n- Prominent forehead\n- Broad fingertip\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/04836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Mandibular prognathia\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Telecanthus\n- Cataract\n- Abnormality of the ear\n- Autism\n- Pectus excavatum\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Limitation of joint mobility\n- Pericarditis\n- Broad-based gait\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Microtia\n- Abnormality of the gastrointestinal tract\n- Broad eyebrow\n- Midface retrusion\n- Camptodactyly\n- Abnormality of brain morphology\n- Clinodactyly\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/04837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Talipes equinovarus\n- Broad toe\n- Hip dislocation\n- Knee dislocation\n- Bilateral elbow dislocations\n- Depressed nasal bridge\n- Vertebral wedging\n- Prominent forehead\n- Broad fingertip\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/04839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/04840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/04841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/04842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/04843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/04847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/04858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/04859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/04860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/04861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/04862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/04863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/04872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/04905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/04906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Prominent scalp veins\n- Low hanging columella\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/04907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Prominent scalp veins\n- Low hanging columella\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/04908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/04909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/04910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/04911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/04912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/04913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/04914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/04932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the outer ear\n- Hearing impairment\n- Retinal coloboma\n- Delayed puberty\n- Growth delay\n- Partial atrioventricular canal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormality of the outer ear\n- Hearing impairment\n- Incomplete partition of the cochlea type II\n- Choanal stenosis\n- Iris coloboma\n- Macular coloboma\n- Ventricular septal defect\n- Pulmonary valve atresia\n- Submucous cleft of soft and hard palate\n- Bilateral facial palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the outer ear\n- Abnormality of the inner ear\n- Hearing impairment\n- Choanal atresia\n- Optic disc coloboma\n- Patent ductus arteriosus\n- Abnormality of the male genitalia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/04951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/04962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/04973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Pointed chin\n- Hypertelorism\n- Low-set ears\n- Thickened helices\n- Webbed neck\n- Short neck\n- Downslanted palpebral fissures\n- Ptosis\n- Abnormal sternum morphology\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Abnormal heart morphology\n- Atrial septal defect\n- Pes planus\n- Low posterior hairline\n- Chiari malformation\n- Short stature\n- Postnatal growth retardation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/04974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/04981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/04999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05039.png"} 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diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/05048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/05061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/05062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/05063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/05064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/05065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/05066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/05067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Thickened helices\n- Dental malocclusion\n- Delayed speech and language development\n- Intellectual disability, moderate\n- Spotty hyperpigmentation\n- Persistence of primary teeth\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Thickened helices\n- Dental malocclusion\n- Delayed speech and language development\n- Intellectual disability, moderate\n- Spotty hyperpigmentation\n- Persistence of primary teeth\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Congenital diaphragmatic hernia\n- Partial agenesis of the corpus callosum\n- Bicoronal synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Hypertelorism\n- Low-set ears\n- Downslanted palpebral fissures\n- Ptosis\n- Sprengel anomaly\n- Brachydactyly\n- Intellectual disability, mild\n- Agenesis of corpus callosum\n- Ridged nail\n- Midline nasal groove\n- Clinodactyly of the 5th finger\n- Coronal craniosynostosis\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Hypertelorism\n- Low-set ears\n- Downslanted palpebral fissures\n- Ptosis\n- Sprengel anomaly\n- Brachydactyly\n- Intellectual disability, mild\n- Agenesis of corpus callosum\n- Ridged nail\n- Midline nasal groove\n- Clinodactyly of the 5th finger\n- Coronal craniosynostosis\n- Unilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Downslanted palpebral fissures\n- Brachydactyly\n- Agenesis of corpus callosum\n- Specific learning disability\n- Ridged nail\n- Midline nasal groove\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Downslanted palpebral fissures\n- Brachydactyly\n- Agenesis of corpus callosum\n- Specific learning disability\n- Ridged nail\n- Midline nasal groove\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Downslanted palpebral fissures\n- Midline nasal groove\n- Clinodactyly of the 5th finger\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Downslanted palpebral fissures\n- Midline nasal groove\n- Clinodactyly of the 5th finger\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/05091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/05092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/05093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/05119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genital system\n- Microcephaly\n- Hearing impairment\n- Atypical behavior\n- Seizure\n- Intellectual disability, moderate\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/05156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short long bone\n- Dislocated radial head\n- Persistence of primary teeth\n- Limb undergrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short long bone\n- Dislocated radial head\n- Persistence of primary teeth\n- Limb undergrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Proptosis\n- Intrauterine growth retardation\n- Frontal bossing\n- Short long bone\n- Mesomelia\n- Short stature\n- Depressed nasal bridge\n- Bilateral cryptorchidism\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Proptosis\n- Intrauterine growth retardation\n- Frontal bossing\n- Short long bone\n- Mesomelia\n- Short stature\n- Depressed nasal bridge\n- Bilateral cryptorchidism\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Proptosis\n- Intrauterine growth retardation\n- Frontal bossing\n- Short long bone\n- Mesomelia\n- Short stature\n- Depressed nasal bridge\n- Bilateral cryptorchidism\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Malar flattening\n- Hypertelorism\n- Micrognathia\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Proptosis\n- Intrauterine growth retardation\n- Frontal bossing\n- Short long bone\n- Mesomelia\n- Short stature\n- Depressed nasal bridge\n- Bilateral cryptorchidism\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/05187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/05188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/05189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/05190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/05191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/05192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/05193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/05194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/05195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/05196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/05197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/05213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/05220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/05221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/05222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/05223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/05224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/05225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/05226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Poor fine motor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/05227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Sacral dimple\n- Generalized hypotonia\n- Pes planus\n- Poor motor coordination\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/05228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocele testis\n- Enlarged kidney\n- Hydronephrosis\n- Wide mouth\n- Furrowed tongue\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Delayed speech and language development\n- Pectus excavatum\n- Abnormality of the vertebral column\n- Large hands\n- Motor delay\n- Large for gestational age\n- Umbilical hernia\n- Abnormal heart morphology\n- Ventricular septal defect\n- Hepatomegaly\n- High, narrow palate\n- Accelerated skeletal maturation\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocele testis\n- Enlarged kidney\n- Hydronephrosis\n- Wide mouth\n- Furrowed tongue\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Delayed speech and language development\n- Pectus excavatum\n- Abnormality of the vertebral column\n- Large hands\n- Motor delay\n- Large for gestational age\n- Umbilical hernia\n- Abnormal heart morphology\n- Ventricular septal defect\n- Hepatomegaly\n- High, narrow palate\n- Accelerated skeletal maturation\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydroureter\n- Enlarged kidney\n- Hydronephrosis\n- Wide mouth\n- Furrowed tongue\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Delayed speech and language development\n- Pectus excavatum\n- Abnormality of the vertebral column\n- Large hands\n- Motor delay\n- Large for gestational age\n- Umbilical hernia\n- Hepatomegaly\n- High, narrow palate\n- Accelerated skeletal maturation\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/05256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/05257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/05258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/05259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/05260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/05261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/05262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/05263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/05264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/05265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/05266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/05267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/05268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Strabismus\n- Visual impairment\n- Thick eyebrow\n- Agitation\n- Autism\n- Compulsive behaviors\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Slender finger\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Slender build\n- Weight loss\n- Constipation\n- Loss of speech\n- Developmental regression\n- Scoliosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Attention deficit hyperactivity disorder\n- Cervical instability\n- Tented upper lip vermilion\n- Upturned corners of mouth\n- Tented philtrum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Polyuria\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Abnormal nasal bridge morphology\n- Short attention span\n- Pectus carinatum\n- Gait disturbance\n- Ventricular septal defect\n- Tachycardia\n- Patent foramen ovale\n- Prolonged QT interval\n- Overlapping toe\n- Poor coordination\n- Supraventricular tachycardia\n- Hyperextensible hand joints\n- Abnormal aggressive, impulsive or violent behavior\n- Six lumbar vertebrae\n- Feeding difficulties in infancy\n- Generalized neonatal hypotonia\n- Thin lower lip vermilion\n- Ankle clonus\n- obsolete Toe walking\n- Cerebral palsy\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Anxiety\n- Delayed speech and language development\n- Slender finger\n- Motor delay\n- Slender build\n- Congestive heart failure\n- Tetralogy of Fallot\n- Pulmonic stenosis\n- Asplenia\n- Single ventricle\n- Headache\n- Developmental regression\n- Episodic vomiting\n- Abnormal muscle tone\n- Short stature\n- Prominent nasal tip\n- Capillary hemangioma\n- Poor fine motor coordination\n- Feeding difficulties in infancy\n- Horizontal eyebrow\n- Long upper lip\n- Mild global developmental delay\n- Tricuspid atresia\n- Left superior vena cava draining directly to the left atrium\n- Abnormal aortic arch morphology\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Anxiety\n- Low frustration tolerance\n- Delayed speech and language development\n- Eczema\n- Intellectual disability\n- Lethargy\n- Motor delay\n- Dandy-Walker malformation\n- Rigidity\n- Poor motor coordination\n- Headache\n- Sleep disturbance\n- Poor fine motor coordination\n- Repetitive compulsive behavior\n- Astrocytoma\n- Pulmonary insufficiency\n- Mild global developmental delay\n- Tetralogy of Fallot with pulmonary stenosis\n- Tetralogy of Fallot with pulmonary atresia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Full cheeks\n- Low-set ears\n- Long eyelashes\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Pectus excavatum\n- Sacral dimple\n- Urticaria\n- Mottled pigmentation\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Craniosynostosis\n- Prolonged QT interval\n- Gastroesophageal reflux\n- Gait imbalance\n- Delayed CNS myelination\n- Drooling\n- Unsteady gait\n- Abnormal periventricular white matter morphology\n- Bowel incontinence\n- Elevated circulating alkaline phosphatase concentration\n- Neonatal hyperbilirubinemia\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Self-biting\n- Snout reflex\n- Systolic heart murmur\n- Decreased body fat percentage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Full cheeks\n- Low-set ears\n- Long eyelashes\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Pectus excavatum\n- Sacral dimple\n- Urticaria\n- Mottled pigmentation\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Craniosynostosis\n- Prolonged QT interval\n- Gastroesophageal reflux\n- Gait imbalance\n- Delayed CNS myelination\n- Drooling\n- Unsteady gait\n- Abnormal periventricular white matter morphology\n- Bowel incontinence\n- Elevated circulating alkaline phosphatase concentration\n- Neonatal hyperbilirubinemia\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Self-biting\n- Snout reflex\n- Systolic heart murmur\n- Decreased body fat percentage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Abnormality of the anterior fontanelle\n- Microcephaly\n- Full cheeks\n- Facial asymmetry\n- Low-set ears\n- Otitis media\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Astigmatism\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Esotropia\n- Thick eyebrow\n- Amblyopia\n- Delayed speech and language development\n- Eczema\n- Hirsutism\n- Mottled pigmentation\n- Prominent fingertip pads\n- Seizure\n- Global developmental delay\n- Motor delay\n- Abnormal corpus callosum morphology\n- Syncope\n- Failure to thrive\n- Polyhydramnios\n- Premature birth\n- Breech presentation\n- Prolonged QT interval\n- Bradycardia\n- Dysphagia\n- Pneumonia\n- Apnea\n- Abnormal cerebral ventricle morphology\n- Ventriculomegaly\n- Drooling\n- Abnormal periventricular white matter morphology\n- Hypoplastic nipples\n- Neonatal respiratory distress\n- Recurrent upper respiratory tract infections\n- Tachypnea\n- Obstructive sleep apnea\n- Beaking of vertebral bodies\n- Flat occiput\n- Feeding difficulties in infancy\n- Uplifted earlobe\n- Intellectual disability, severe\n- Self-biting\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Smooth philtrum\n- Cupped ear\n- Strabismus\n- Delayed speech and language development\n- Eczema\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Pericardial effusion\n- Pneumonia\n- Frequent falls\n- Hypercalcemia\n- Short stature\n- Periventricular leukomalacia\n- Double tooth\n- Prominent eyelashes\n- Abnormality of upper lip vermillion\n- Feeding difficulties\n- Allergy\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Smooth philtrum\n- Cupped ear\n- Strabismus\n- Delayed speech and language development\n- Eczema\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Pericardial effusion\n- Pneumonia\n- Frequent falls\n- Hypercalcemia\n- Short stature\n- Periventricular leukomalacia\n- Double tooth\n- Prominent eyelashes\n- Abnormality of upper lip vermillion\n- Feeding difficulties\n- Allergy\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Smooth philtrum\n- Cupped ear\n- Strabismus\n- Delayed speech and language development\n- Eczema\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Pericardial effusion\n- Pneumonia\n- Frequent falls\n- Hypercalcemia\n- Short stature\n- Periventricular leukomalacia\n- Double tooth\n- Prominent eyelashes\n- Abnormality of upper lip vermillion\n- Feeding difficulties\n- Allergy\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Dolichocephaly\n- Full cheeks\n- Microretrognathia\n- Triangular face\n- Broad forehead\n- High forehead\n- Posteriorly rotated ears\n- Otitis media\n- Prominent nasal bridge\n- Narrow nasal bridge\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Iris coloboma\n- Amblyopia\n- Autism\n- Short attention span\n- Delayed speech and language development\n- Slender finger\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Slurred speech\n- Craniosynostosis\n- Joint laxity\n- Gastroesophageal reflux\n- Prominent glabella\n- Poor motor coordination\n- Expressive language delay\n- Decreased plasma carnitine\n- Attention deficit hyperactivity disorder\n- Few cafe-au-lait spots\n- Hypermobility of toe joints\n- Speech apraxia\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Dolichocephaly\n- Hearing impairment\n- Recurrent otitis media\n- Hypermetropia\n- Autism\n- Aggressive behavior\n- Delayed speech and language development\n- Seizure\n- Intellectual disability, mild\n- Global developmental delay\n- Macrodontia\n- Gastroesophageal reflux\n- Frequent falls\n- Intestinal malrotation\n- High, narrow palate\n- Osteomyelitis\n- Short stature\n- Attention deficit hyperactivity disorder\n- Abnormal hair whorl\n- Recurrent sinusitis\n- Nasogastric tube feeding in infancy\n- Feeding difficulties\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Tall stature\n- Conductive hearing impairment\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Synophrys\n- Generalized hypotonia\n- Failure to thrive\n- Fever\n- Constipation\n- Delayed gross motor development\n- Short stature\n- Feeding difficulties in infancy\n- Tented philtrum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Wide nasal bridge\n- Fair hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Wide nasal bridge\n- Fair hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Prominent nose\n- Long eyelashes\n- Dry skin\n- Global developmental delay\n- Motor delay\n- Pes cavus\n- Dysphagia\n- Cerebral atrophy\n- Gait imbalance\n- Intellectual disability, moderate\n- Frequent falls\n- Expressive language delay\n- Short femur\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n- Anxiety\n- Delayed speech and language development\n- Long eyebrows\n- Delayed fine motor development\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/05304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Short philtrum\n- Widow's peak\n- Small forehead\n- Bulbous nose\n- Astigmatism\n- Proptosis\n- Thick eyebrow\n- Synophrys\n- Hyperactivity\n- Pectus excavatum\n- Precocious puberty\n- Seizure\n- Bicuspid aortic valve\n- Prolonged QT interval\n- Dysphagia\n- Gastroesophageal reflux\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Widened subarachnoid space\n- Cerebral white matter agenesis\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Short philtrum\n- Widow's peak\n- Small forehead\n- Bulbous nose\n- Astigmatism\n- Proptosis\n- Thick eyebrow\n- Synophrys\n- Hyperactivity\n- Pectus excavatum\n- Precocious puberty\n- Seizure\n- Bicuspid aortic valve\n- Prolonged QT interval\n- Dysphagia\n- Gastroesophageal reflux\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Widened subarachnoid space\n- Cerebral white matter agenesis\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Short philtrum\n- Widow's peak\n- Small forehead\n- Bulbous nose\n- Astigmatism\n- Proptosis\n- Thick eyebrow\n- Synophrys\n- Hyperactivity\n- Pectus excavatum\n- Precocious puberty\n- Seizure\n- Bicuspid aortic valve\n- Prolonged QT interval\n- Dysphagia\n- Gastroesophageal reflux\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Widened subarachnoid space\n- Cerebral white matter agenesis\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Short philtrum\n- Widow's peak\n- Small forehead\n- Bulbous nose\n- Astigmatism\n- Proptosis\n- Thick eyebrow\n- Synophrys\n- Hyperactivity\n- Pectus excavatum\n- Precocious puberty\n- Seizure\n- Bicuspid aortic valve\n- Prolonged QT interval\n- Dysphagia\n- Gastroesophageal reflux\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Widened subarachnoid space\n- Cerebral white matter agenesis\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Short philtrum\n- Widow's peak\n- Small forehead\n- Bulbous nose\n- Astigmatism\n- Proptosis\n- Thick eyebrow\n- Synophrys\n- Hyperactivity\n- Pectus excavatum\n- Precocious puberty\n- Seizure\n- Bicuspid aortic valve\n- Prolonged QT interval\n- Dysphagia\n- Gastroesophageal reflux\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Widened subarachnoid space\n- Cerebral white matter agenesis\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Thick eyebrow\n- Agitation\n- Precocious puberty\n- Intellectual disability\n- Bradycardia\n- Vomiting\n- Gastrointestinal dysmotility\n- Elevated circulating follicle stimulating hormone level\n- Intracranial cystic lesion\n- Delayed fine motor development\n- Self-biting\n- Episodic fatigue\n- Small intestinal bacterial overgrowth\n- Tube feeding\n- Cerebral visual impairment\n- Body odor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Thick eyebrow\n- Agitation\n- Precocious puberty\n- Intellectual disability\n- Bradycardia\n- Vomiting\n- Gastrointestinal dysmotility\n- Elevated circulating follicle stimulating hormone level\n- Intracranial cystic lesion\n- Delayed fine motor development\n- Self-biting\n- Episodic fatigue\n- Small intestinal bacterial overgrowth\n- Tube feeding\n- Cerebral visual impairment\n- Body odor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Thick eyebrow\n- Agitation\n- Precocious puberty\n- Intellectual disability\n- Bradycardia\n- Vomiting\n- Gastrointestinal dysmotility\n- Elevated circulating follicle stimulating hormone level\n- Intracranial cystic lesion\n- Delayed fine motor development\n- Self-biting\n- Episodic fatigue\n- Small intestinal bacterial overgrowth\n- Tube feeding\n- Cerebral visual impairment\n- Body odor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Thick eyebrow\n- Agitation\n- Precocious puberty\n- Intellectual disability\n- Bradycardia\n- Vomiting\n- Gastrointestinal dysmotility\n- Elevated circulating follicle stimulating hormone level\n- Intracranial cystic lesion\n- Delayed fine motor development\n- Self-biting\n- Episodic fatigue\n- Small intestinal bacterial overgrowth\n- Tube feeding\n- Cerebral visual impairment\n- Body odor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad philtrum\n- Short philtrum\n- Micrognathia\n- Hearing impairment\n- Thick eyebrow\n- Agitation\n- Precocious puberty\n- Intellectual disability\n- Bradycardia\n- Vomiting\n- Gastrointestinal dysmotility\n- Elevated circulating follicle stimulating hormone level\n- Intracranial cystic lesion\n- Delayed fine motor development\n- Self-biting\n- Episodic fatigue\n- Small intestinal bacterial overgrowth\n- Tube feeding\n- Cerebral visual impairment\n- Body odor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad philtrum\n- Short philtrum\n- Astigmatism\n- Inflexible adherence to routines or rituals\n- Anxiety\n- Delayed speech and language development\n- Cutis marmorata\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Vomiting\n- Sleep disturbance\n- Gastrointestinal dysmotility\n- Prolonged QTc interval\n- Pica\n- Allergy\n- Food intolerance\n- Auditory sensitivity\n- Mallory-Weiss tear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Broad philtrum\n- Hypertelorism\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Proptosis\n- Hypermetropia\n- Thick eyebrow\n- Reduced eye contact\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Intrauterine growth retardation\n- Omphalocele\n- Ventriculomegaly\n- Intracranial hemorrhage\n- Short nose\n- Abnormal T-wave\n- Focal-onset seizure\n- Reduced visual acuity\n- Laterally extended eyebrow\n- Feeding difficulties\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Broad philtrum\n- Hypertelorism\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Proptosis\n- Hypermetropia\n- Thick eyebrow\n- Reduced eye contact\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Intrauterine growth retardation\n- Omphalocele\n- Ventriculomegaly\n- Intracranial hemorrhage\n- Short nose\n- Abnormal T-wave\n- Focal-onset seizure\n- Reduced visual acuity\n- Laterally extended eyebrow\n- Feeding difficulties\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Broad philtrum\n- Hypertelorism\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Proptosis\n- Hypermetropia\n- Thick eyebrow\n- Reduced eye contact\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Intrauterine growth retardation\n- Omphalocele\n- Ventriculomegaly\n- Intracranial hemorrhage\n- Short nose\n- Abnormal T-wave\n- Focal-onset seizure\n- Reduced visual acuity\n- Laterally extended eyebrow\n- Feeding difficulties\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Broad philtrum\n- Hypertelorism\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Proptosis\n- Hypermetropia\n- Thick eyebrow\n- Reduced eye contact\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Intrauterine growth retardation\n- Omphalocele\n- Ventriculomegaly\n- Intracranial hemorrhage\n- Short nose\n- Abnormal T-wave\n- Focal-onset seizure\n- Reduced visual acuity\n- Laterally extended eyebrow\n- Feeding difficulties\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Broad philtrum\n- Hypertelorism\n- Long philtrum\n- Anteverted nares\n- Astigmatism\n- Proptosis\n- Hypermetropia\n- Thick eyebrow\n- Reduced eye contact\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Intrauterine growth retardation\n- Omphalocele\n- Ventriculomegaly\n- Intracranial hemorrhage\n- Short nose\n- Abnormal T-wave\n- Focal-onset seizure\n- Reduced visual acuity\n- Laterally extended eyebrow\n- Feeding difficulties\n- Tall chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/05372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/05373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/05374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/05375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/05376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/05377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/05378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/05379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/05382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/05383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/05384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/05385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/05386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/05413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/05414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/05415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/05422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/05429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/05430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/05431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/05432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/05433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/05434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/05435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/05436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/05437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/05469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/05470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/05471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Thick eyebrow\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Brachydactyly\n- Seizure\n- Abnormal facial shape\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Focal-onset seizure\n- Intellectual disability, severe\n- Incisor macrodontia\n- Prominent eyelashes\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/05478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/05479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/05483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/05484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/05485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/05486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/05487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/05488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/05489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/05490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/05491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/05492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/05493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/05494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/05495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent nose\n- Downslanted palpebral fissures\n- Cataract\n- Sclerocornea\n- Hirsutism\n- Intrauterine growth retardation\n- Abnormal pulmonary valve morphology\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Right ventricular hypertrophy\n- Constipation\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Short stature\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Broad thumb\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent nose\n- Downslanted palpebral fissures\n- Cataract\n- Sclerocornea\n- Hirsutism\n- Intrauterine growth retardation\n- Abnormal pulmonary valve morphology\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Right ventricular hypertrophy\n- Constipation\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Short stature\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Broad thumb\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent nose\n- Downslanted palpebral fissures\n- Cataract\n- Sclerocornea\n- Hirsutism\n- Intrauterine growth retardation\n- Abnormal pulmonary valve morphology\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Right ventricular hypertrophy\n- Constipation\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Short stature\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Broad thumb\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Prominent nose\n- Astigmatism\n- Myopia\n- Intellectual disability, mild\n- Short stature\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent nose\n- Strabismus\n- Downslanted palpebral fissures\n- Hirsutism\n- Intrauterine growth retardation\n- Patent ductus arteriosus\n- Tethered cord\n- Scoliosis\n- Short stature\n- Premature ovarian insufficiency\n- Bilateral sensorineural hearing impairment\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Intellectual disability, severe\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent nose\n- Strabismus\n- Downslanted palpebral fissures\n- Hirsutism\n- Intrauterine growth retardation\n- Patent ductus arteriosus\n- Tethered cord\n- Scoliosis\n- Short stature\n- Premature ovarian insufficiency\n- Bilateral sensorineural hearing impairment\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Intellectual disability, severe\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent nose\n- Strabismus\n- Downslanted palpebral fissures\n- Hirsutism\n- Intrauterine growth retardation\n- Patent ductus arteriosus\n- Tethered cord\n- Scoliosis\n- Short stature\n- Premature ovarian insufficiency\n- Bilateral sensorineural hearing impairment\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad hallux\n- Intellectual disability, severe\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Coarse facial features\n- Dental crowding\n- Dysarthria\n- Joint hypermobility\n- Hepatic steatosis\n- Scoliosis\n- Arthralgia\n- Patellar dislocation\n- Persistent left superior vena cava\n- Bilateral conductive hearing impairment\n- Feeding difficulties in infancy\n- Frontal hirsutism\n- Low femoral bone density\n- Spondylitis\n- Absent fifth toenail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/05540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/05541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/05542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/05543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/05544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/05545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/05546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/05547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/05548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/05551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/05552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/05556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/05557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/05559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/05569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/05570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/05571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/05572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/05584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Synophrys\n- Hirsutism\n- Global developmental delay\n- Short nose\n- Concave nasal ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Prominent nasal bridge\n- Myopia\n- Thick eyebrow\n- Synophrys\n- Dental crowding\n- Hypothyroidism\n- Back pain\n- Short 5th finger\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Anteverted nares\n- Thick eyebrow\n- Congenital diaphragmatic hernia\n- Global developmental delay\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/05613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Hearing impairment\n- Conductive hearing impairment\n- Protruding ear\n- Bulbous nose\n- Telecanthus\n- Thick eyebrow\n- Synophrys\n- Delayed speech and language development\n- Motor delay\n- Abnormal heart morphology\n- Ventricular septal defect\n- Abnormal aortic valve morphology\n- Deep philtrum\n- Short stature\n- Preauricular pit\n- Long eyebrows\n- Abnormal renal pelvis morphology\n- Feeding difficulties\n- Pilomatrixoma\n- Anteverted ears\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Hearing impairment\n- Conductive hearing impairment\n- Bulbous nose\n- Telecanthus\n- Synophrys\n- Hypertrichosis\n- Brachydactyly\n- Intellectual disability\n- Macrodontia\n- Dysphonia\n- Deep philtrum\n- Gastroesophageal reflux\n- Short stature\n- Long eyebrows\n- Incisor macrodontia\n- Broad eyebrow\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Bulbous nose\n- Telecanthus\n- Synophrys\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Motor delay\n- Macrodontia\n- Mitral regurgitation\n- Deep philtrum\n- Gastroesophageal reflux\n- Short stature\n- Long eyebrows\n- Incisor macrodontia\n- Broad eyebrow\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Bulbous nose\n- Synophrys\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Macrodontia\n- Deep philtrum\n- Scoliosis\n- Short stature\n- Long eyebrows\n- Incisor macrodontia\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Bulbous nose\n- Telecanthus\n- Synophrys\n- Delayed speech and language development\n- Hypertrichosis\n- Brachydactyly\n- Intellectual disability\n- Macrodontia\n- Deep philtrum\n- Clinodactyly of the 5th finger\n- Short stature\n- Long eyebrows\n- Incisor macrodontia\n- Broad eyebrow\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/05632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypogonadotropic hypogonadism\n- Abnormal pinna morphology\n- Cupped ear\n- Sensorineural hearing impairment\n- Depressed nasal tip\n- Choanal atresia\n- Broad nasal tip\n- Hypoplasia of teeth\n- Hypothyroidism\n- Decreased response to growth hormone stimulation test\n- Global developmental delay\n- Growth delay\n- Hypoplastic nipples\n- Facial palsy\n- Aplasia of the semicircular canal\n- Aplasia\/Hypoplasia of the pancreas\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/05645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/05646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High palate\n- Brachycephaly\n- Long philtrum\n- High forehead\n- Astigmatism\n- Visual impairment\n- Telecanthus\n- Upslanted palpebral fissure\n- Horizontal nystagmus\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Deep philtrum\n- Bilateral tonic-clonic seizure\n- Sparse scalp hair\n- Exaggerated cupid's bow\n- Highly arched eyebrow\n- Depressed nasal bridge\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/05647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/05648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/05649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/05657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/05679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/05680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/05681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/05682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/05683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/05684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/05686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/05687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Small face\n- Triangular face\n- Otitis media\n- Delayed speech and language development\n- Nephrolithiasis\n- Hematuria\n- Brachydactyly\n- Seizure\n- Global developmental delay\n- Failure to thrive\n- Patent foramen ovale\n- Delayed skeletal maturation\n- Elfin facies\n- Delayed fine motor development\n- Chronic sinusitis\n- Dysuria\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/05688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/05693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/05694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/05695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/05696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/05697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/05698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/05702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Convex nasal ridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Thick eyebrow\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Motor delay\n- Specific learning disability\n- Brisk reflexes\n- Flexion contracture\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Limb hypertonia\n- Episodic vomiting\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/05756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/05766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/05767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/05768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/05769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/05777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/05778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/05781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/05782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/05783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/05786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/05787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/05788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/05789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/05790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/05791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/05792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/05793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/05794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/05795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Astigmatism\n- Myopia\n- Delayed speech and language development\n- Narrow chest\n- Primary hypothyroidism\n- Motor delay\n- Neonatal hypotonia\n- Joint laxity\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/05801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Astigmatism\n- Myopia\n- Delayed speech and language development\n- Narrow chest\n- Primary hypothyroidism\n- Motor delay\n- Neonatal hypotonia\n- Joint laxity\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/05802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/05811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/05815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/05817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/05818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/05819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/05820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/05821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/05823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/05826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/05827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/05828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/05829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/05830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/05831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/05834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/05835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/05836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/05837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/05838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/05839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/05840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/05841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/05849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/05850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/05851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/05852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/05853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/05854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/05855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/05856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/05857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/05858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/05859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/05860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/05874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/05875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/05877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/05878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/05879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/05880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Stenosis of the external auditory canal\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Lower eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/05881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/05885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/05886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/05887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/05889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/05892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/05893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/05894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/05895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/05896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/05897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/05898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/05899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/05900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/05901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/05902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/05906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/05907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/05911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/05912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/05913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/05914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/05915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/05916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/05917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/05918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/05919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/05920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/05921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/05922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/05942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/05943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/05944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/05945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/05946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/05947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/05948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/05949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/05950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/05951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/05952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/05953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/05954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/05958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/05960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/05962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/05967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/05968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/05969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/05970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/05971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/05972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/05973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/05974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/05975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/05976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/05977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Abnormality of the nose\n- Myopia\n- Abnormal fingertip morphology\n- Seizure\n- Global developmental delay\n- Failure to thrive\n- Toe syndactyly\n- Constipation\n- Abnormal cerebral ventricle morphology\n- Abnormal muscle tone\n- Abnormal cheek morphology\n- Feeding difficulties\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/05978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular face\n- Exotropia\n- Delayed speech and language development\n- Cafe-au-lait spot\n- Motor delay\n- Failure to thrive\n- Scoliosis\n- Thoracic kyphosis\n- Thoracolumbar scoliosis\n- Increased LDL cholesterol concentration\n- Decreased HDL cholesterol concentration\n- Increased muscle fatiguability\n- Vertebral wedging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/05979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/05984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/05989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/05990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/05991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/05992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Recurrent otitis media\n- Wide nasal bridge\n- Intellectual disability\n- Failure to thrive\n- Intrauterine growth retardation\n- Chronic diarrhea\n- Woolly hair\n- Elevated hepatic transaminase\n- Recurrent pneumonia\n- Prominent forehead\n- Villous atrophy\n- Hepatic bridging fibrosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/05993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/05994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/05995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/05996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/05997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/05998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/05999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/06000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/06001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/06002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/06003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/06004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/06015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/06016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/06017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/06018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/06019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/06020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/06035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/06036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/06037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/06053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/06054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/06061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/06068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/06069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/06070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/06071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/06072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/06073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/06074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Short philtrum\n- Hearing impairment\n- Deeply set eye\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Intellectual disability\n- Clinodactyly of the 5th finger\n- Prominent proximal interphalangeal joints\n- Large earlobe\n- Low hanging columella\n- Medial flaring of the eyebrow\n- Broad columella\n- Simple ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Broad forehead\n- Hearing impairment\n- Downslanted palpebral fissures\n- Intellectual disability\n- Frontal bossing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Broad forehead\n- Hearing impairment\n- Downslanted palpebral fissures\n- Intellectual disability\n- Frontal bossing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Malar flattening\n- Downslanted palpebral fissures\n- Ventricular septal defect\n- Atrial septal defect\n- Short forearm\n- Aplasia\/Hypoplasia of the mandible\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tinnitus\n- Hearing impairment\n- Intellectual disability, mild\n- Specific learning disability\n- Gastroesophageal reflux\n- Vertigo\n- Memory impairment\n- Spastic\/hyperactive bladder\n- Recurrent sinusitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Thin vermilion border\n- Abnormality of the philtrum\n- Hypertelorism\n- Bulbous nose\n- Anteverted nares\n- Atypical behavior\n- Seizure\n- Global developmental delay\n- Exaggerated cupid's bow\n- EEG abnormality\n- Thick nasal alae\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Round face\n- Hypertelorism\n- Prominent nose\n- Synophrys\n- Atypical behavior\n- Abnormality of the hand\n- Brachydactyly\n- Seizure\n- Global developmental delay\n- EEG abnormality\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Incisor macrodontia\n- Prominence of the zygomatic bone\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Velopharyngeal insufficiency\n- Thin vermilion border\n- Microcephaly\n- Abnormality of the philtrum\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Atypical behavior\n- Abnormality of the hand\n- Brachydactyly\n- Seizure\n- Global developmental delay\n- Macrodontia\n- Abnormal heart morphology\n- Intellectual disability, moderate\n- EEG abnormality\n- Delayed skeletal maturation\n- Caudal appendage\n- Clinodactyly of the 5th finger\n- Thick nasal alae\n- Incisor macrodontia\n- Abnormality of upper lip vermillion\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin upper lip vermilion\n- Thin vermilion border\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Abnormality of the hand\n- Brachydactyly\n- Global developmental delay\n- Umbilical hernia\n- Macrodontia\n- Exaggerated cupid's bow\n- Clinodactyly of the 5th finger\n- Intellectual disability, borderline\n- Thick nasal alae\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Thin vermilion border\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Atypical behavior\n- Abnormality of the hand\n- Global developmental delay\n- Macrodontia\n- Exaggerated cupid's bow\n- Sleep disturbance\n- Intellectual disability, borderline\n- Thick nasal alae\n- Morbus Scheuermann\n- Incisor macrodontia\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Abnormality of the philtrum\n- Hearing impairment\n- Bulbous nose\n- Anteverted nares\n- Precocious puberty\n- Abnormality of the hand\n- Intellectual disability, mild\n- Global developmental delay\n- Macrodontia\n- Exaggerated cupid's bow\n- Delayed skeletal maturation\n- Thick nasal alae\n- Incisor macrodontia\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Prominent nasal bridge\n- Prominent nose\n- Synophrys\n- Seizure\n- Global developmental delay\n- Intellectual disability, moderate\n- EEG abnormality\n- Short stature\n- Acute myeloid leukemia\n- Prominence of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Thin vermilion border\n- Microcephaly\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Atypical behavior\n- Precocious puberty\n- Abnormality of the hand\n- Intellectual disability, mild\n- Global developmental delay\n- Macrodontia\n- Morphological central nervous system abnormality\n- Exaggerated cupid's bow\n- Sleep disturbance\n- Thick nasal alae\n- Incisor macrodontia\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Prominent nasal bridge\n- Prominent nose\n- Synophrys\n- Abnormality of the hand\n- Brachydactyly\n- Global developmental delay\n- Abnormal heart morphology\n- Intellectual disability, moderate\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Short stature\n- Prominence of the zygomatic bone\n- Camptodactyly\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydroureter\n- Thin upper lip vermilion\n- Thin vermilion border\n- Microcephaly\n- Abnormality of the philtrum\n- Round face\n- Hypertelorism\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Global developmental delay\n- Abnormal heart morphology\n- Morphological central nervous system abnormality\n- Exaggerated cupid's bow\n- Sleep disturbance\n- Short stature\n- Thick nasal alae\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Round face\n- Hypertelorism\n- Prominent nasal bridge\n- Prominent nose\n- Synophrys\n- Atypical behavior\n- Abnormality of the hand\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Macrodontia\n- Abnormal heart morphology\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Incisor macrodontia\n- Prominence of the zygomatic bone\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Velopharyngeal insufficiency\n- Thin vermilion border\n- Round face\n- Hypertelorism\n- Hearing impairment\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Atypical behavior\n- Precocious puberty\n- Abnormality of the hand\n- Global developmental delay\n- Macrodontia\n- Exaggerated cupid's bow\n- Delayed skeletal maturation\n- Intellectual disability, borderline\n- Thick nasal alae\n- Incisor macrodontia\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal agenesis\n- Thin upper lip vermilion\n- Thin vermilion border\n- Abnormality of the philtrum\n- Round face\n- Hypertelorism\n- Hearing impairment\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Atypical behavior\n- Seizure\n- Global developmental delay\n- Macrodontia\n- Morphological central nervous system abnormality\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- EEG abnormality\n- Sleep disturbance\n- Scoliosis\n- Short stature\n- Thick nasal alae\n- Incisor macrodontia\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Round face\n- Hypertelorism\n- Prominent nasal bridge\n- Prominent nose\n- Synophrys\n- Atypical behavior\n- Precocious puberty\n- Abnormality of the hand\n- Seizure\n- Intellectual disability, mild\n- Global developmental delay\n- EEG abnormality\n- Sleep disturbance\n- Short stature\n- Prominence of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Cutis marmorata\n- Hirsutism\n- Intellectual disability\n- Global developmental delay\n- Plagiocephaly\n- Short foot\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- High, narrow palate\n- Limited elbow movement\n- Clinodactyly of the 5th finger\n- Short palm\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Low anterior hairline\n- Prominent nasal bridge\n- Ptosis\n- Long eyelashes\n- Synophrys\n- Hirsutism\n- Global developmental delay\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Intellectual disability, moderate\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- High, narrow palate\n- Downturned corners of mouth\n- Limited elbow movement\n- Clinodactyly of the 5th finger\n- Short palm\n- Proximal placement of thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Low anterior hairline\n- Long philtrum\n- Micrognathia\n- Prominent nasal bridge\n- Long eyelashes\n- Synophrys\n- Hirsutism\n- Global developmental delay\n- Short foot\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Enlarged cisterna magna\n- Intellectual disability, moderate\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Highly arched eyebrow\n- High, narrow palate\n- Downturned corners of mouth\n- Limited elbow movement\n- Clinodactyly of the 5th finger\n- Short palm\n- Feeding difficulties in infancy\n- Proximal placement of thumb\n- Barrett esophagus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/06167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/06168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/06169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/06170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/06171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/06172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/06173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/06174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/06177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/06178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/06179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/06180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/06182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/06183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/06193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/06194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/06195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/06199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/06200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/06207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/06208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/06209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypertelorism\n- Wide nasal bridge\n- Intellectual disability\n- Cirrhosis\n- Failure to thrive\n- Ascites\n- Chronic diarrhea\n- Intractable diarrhea\n- Pleural effusion\n- Woolly hair\n- Short stature\n- Decreased body weight\n- Malnutrition\n- T lymphocytopenia\n- Hypopigmentation of hair\n- Trichorrhexis nodosa\n- Respiratory tract infection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/06211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Microretrognathia\n- Long philtrum\n- Whistling appearance\n- Hearing impairment\n- Overfolded helix\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Telecanthus\n- Hypermetropia\n- Laryngomalacia\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Overlapping toe\n- Dyspnea\n- Low posterior hairline\n- Recurrent respiratory infections\n- Drooling\n- Short nose\n- Distal arthrogryposis\n- Deep palmar crease\n- Unilateral ptosis\n- Feeding difficulties in infancy\n- Ulnar deviation of finger\n- Contracture of thumb\n- Sleep apnea\n- Overlapping fingers\n- Dimple chin\n- Short palpebral fissure\n- Flexion contracture of finger\n- Snoring\n- Otitis media with effusion\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/06212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Microretrognathia\n- Long philtrum\n- Whistling appearance\n- Hearing impairment\n- Overfolded helix\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Telecanthus\n- Hypermetropia\n- Laryngomalacia\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Overlapping toe\n- Dyspnea\n- Low posterior hairline\n- Recurrent respiratory infections\n- Drooling\n- Short nose\n- Distal arthrogryposis\n- Deep palmar crease\n- Unilateral ptosis\n- Feeding difficulties in infancy\n- Ulnar deviation of finger\n- Contracture of thumb\n- Sleep apnea\n- Overlapping fingers\n- Dimple chin\n- Short palpebral fissure\n- Flexion contracture of finger\n- Snoring\n- Otitis media with effusion\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/06213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/06218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/06219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/06220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/06221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/06222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/06223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/06224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/06225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/06238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/06239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/06240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/06242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/06243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/06244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/06245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/06246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/06247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/06248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/06249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/06250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/06287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Stenosis of the external auditory canal\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Hypertonia\n- Gait disturbance\n- Abnormal foot morphology\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Supernumerary tooth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Delayed speech and language development\n- Pectus excavatum\n- Arachnodactyly\n- Intellectual disability, mild\n- Hypertonia\n- Gait disturbance\n- Slender build\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Scoliosis\n- Kyphosis\n- Feeding difficulties in infancy\n- Cutaneous syndactyly of toes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- 2-3 finger syndactyly\n- Seizure\n- Intellectual disability, mild\n- Slender build\n- Camptodactyly of toe\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/06319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/06320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/06333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/06334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/06352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/06353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/06374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/06375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n- Constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low anterior hairline\n- Strabismus\n- Deeply set eye\n- Thick eyebrow\n- Synophrys\n- Delayed speech and language development\n- Osteopenia\n- Hirsutism\n- Global developmental delay\n- Gait disturbance\n- Macrodontia\n- Gastroesophageal reflux\n- Gait imbalance\n- Scoliosis\n- Thoracic kyphosis\n- Short stature\n- Abnormal aggressive, impulsive or violent behavior\n- Attention deficit hyperactivity disorder\n- Repetitive compulsive behavior\n- Abnormal position of hair whorl\n- Feeding difficulties\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Hearing impairment\n- Myopia\n- Sacral dimple\n- Neonatal hypotonia\n- Pes planus\n- Poor motor coordination\n- Spina bifida\n- Scoliosis\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n- Mild global developmental delay\n- Tented philtrum\n- Keratosis pilaris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Short chin\n- Prominent nasal bridge\n- Astigmatism\n- Long eyelashes\n- Thick eyebrow\n- Nystagmus\n- Autism\n- Delayed speech and language development\n- Sacral dimple\n- Neonatal hypotonia\n- Macrodontia\n- Pes planus\n- Mild short stature\n- Prominent nasal tip\n- Repetitive compulsive behavior\n- Moderate global developmental delay\n- Ankle clonus\n- Chronic fatigue\n- Clinodactyly\n- Periauricular skin pits\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Chordee\n- Hypertelorism\n- Triangular face\n- Myopia\n- Delayed speech and language development\n- Reduced eye contact\n- Sacral dimple\n- Intellectual disability, mild\n- Slurred speech\n- Abnormal morphology of the pelvis musculature\n- Premature birth\n- Metatarsus adductus\n- Sleep disturbance\n- Immunodeficiency\n- Short stature\n- Flat occiput\n- Abnormality of the palpebral fissures\n- Testicular dysgenesis\n- Feeding difficulties in infancy\n- Mild global developmental delay\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Chronic otitis media\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Delayed closure of the anterior fontanelle\n- Macrodontia\n- Patent foramen ovale\n- Dysphagia\n- Short stature\n- Short finger\n- Hyperextensibility of the knee\n- Anteverted ears\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydrocele testis\n- Thin upper lip vermilion\n- Low anterior hairline\n- Triangular face\n- Low-set ears\n- Macrotia\n- Wide nasal bridge\n- Astigmatism\n- Delayed speech and language development\n- Pectus carinatum\n- Sacral dimple\n- Hirsutism\n- Global developmental delay\n- Ventricular septal defect\n- Tetralogy of Fallot\n- Abnormal aortic morphology\n- Pes planus\n- Gait imbalance\n- Neonatal respiratory distress\n- Tented upper lip vermilion\n- Cerebral palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Anteverted nares\n- Myopia\n- Thick eyebrow\n- Migraine\n- Scoliosis\n- Bowel irritability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Retrognathia\n- Triangular face\n- Wide nasal bridge\n- Anteverted nares\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Failure to thrive\n- Macrodontia\n- Bicuspid aortic valve\n- Patent foramen ovale\n- Large fleshy ears\n- High, narrow palate\n- Short stature\n- Feeding difficulties in infancy\n- Ankyloglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Hypertelorism\n- Hearing impairment\n- Wide nasal bridge\n- Broad nasal tip\n- Long eyelashes\n- Synophrys\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Growth delay\n- Kyphosis\n- Abnormality of temperature regulation\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Abnormality of pain sensation\n- Abnormality of upper lip vermillion\n- Fatigue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Submucous cleft hard palate\n- Hearing impairment\n- Wide nasal bridge\n- Broad nasal tip\n- Myopia\n- Amblyopia\n- Autism\n- Aggressive behavior\n- Reduced eye contact\n- Precocious puberty\n- Global developmental delay\n- Specific learning disability\n- Delayed closure of the anterior fontanelle\n- Failure to thrive\n- Pes planus\n- Toe syndactyly\n- Vomiting\n- Sleep disturbance\n- Kyphosis\n- Short stature\n- Persistent left superior vena cava\n- Feeding difficulties in infancy\n- Short finger\n- Dyslexia\n- Horizontal eyebrow\n- Self-biting\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Hearing impairment\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Synophrys\n- Autism\n- Delayed speech and language development\n- Precocious puberty\n- Seizure\n- Global developmental delay\n- Motor delay\n- Macrodontia\n- Large forehead\n- Mild short stature\n- obsolete Prominent epicanthal folds\n- Chronic constipation\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, mild\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/06396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/06397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/06398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/06402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/06410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/06411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/06412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/06413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/06420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Stenosis of the external auditory canal\n- Bulbous nose\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Hypertrichosis\n- Hypotonia\n- Global developmental delay\n- Patent ductus arteriosus\n- Short foot\n- Frontal upsweep of hair\n- Short palm\n- Short stature\n- Depressed nasal bridge\n- Microtia\n- Short palpebral fissure\n- Clinodactyly\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Stenosis of the external auditory canal\n- Bulbous nose\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Hypertrichosis\n- Hypotonia\n- Global developmental delay\n- Short foot\n- Frontal upsweep of hair\n- Short palm\n- Short stature\n- Depressed nasal bridge\n- Microtia\n- Short palpebral fissure\n- Clinodactyly\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/06434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Concave nail\n- Secondary microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/06435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/06440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Wide nose\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Pectus excavatum\n- Hirsutism\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Toe syndactyly\n- Low posterior hairline\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Sacral hypertrichosis\n- Elbow hypertrichosis\n- Short middle phalanx of finger\n- Curly eyelashes\n- Mild intrauterine growth retardation\n- Short 3rd finger\n- Hypoplasia of the antihelix\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/06447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Micrognathia\n- Hearing impairment\n- Macrotia\n- Protruding ear\n- Strabismus\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Synophrys\n- Hirsutism\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Abnormal heart morphology\n- Sandal gap\n- Memory impairment\n- Thoracic scoliosis\n- Limited elbow movement\n- Clinodactyly of the 5th finger\n- Short stature\n- Sacral hypertrichosis\n- Elbow hypertrichosis\n- Curly eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Facial asymmetry\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Seizure\n- Plagiocephaly\n- Low posterior hairline\n- Intellectual disability, moderate\n- Scoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Facial asymmetry\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Seizure\n- Plagiocephaly\n- Low posterior hairline\n- Intellectual disability, moderate\n- Scoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Strabismus\n- Deeply set eye\n- Nystagmus\n- Pectus excavatum\n- Drooling\n- Intellectual disability, moderate\n- Depressed nasal bridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Macrocephaly\n- Long face\n- Pointed chin\n- Strabismus\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Pectus excavatum\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Frontal bossing\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Cavum septum pellucidum\n- Accelerated skeletal maturation\n- Intellectual disability, severe\n- Prominent forehead\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Macrocephaly\n- Long face\n- Pointed chin\n- Strabismus\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Pectus excavatum\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Frontal bossing\n- Ventriculomegaly\n- Recurrent respiratory infections\n- Cavum septum pellucidum\n- Accelerated skeletal maturation\n- Intellectual disability, severe\n- Prominent forehead\n- Abnormality of brain morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Facial asymmetry\n- Strabismus\n- Downslanted palpebral fissures\n- Global developmental delay\n- Frontal bossing\n- Gastroesophageal reflux\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Facial asymmetry\n- Broad nasal tip\n- Bifid nasal tip\n- Downslanted palpebral fissures\n- Telecanthus\n- Exotropia\n- Nystagmus\n- Sprengel anomaly\n- Partial agenesis of the corpus callosum\n- Split nail\n- Frontal bossing\n- Coarse hair\n- Clinodactyly of the 5th finger\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Facial asymmetry\n- Broad nasal tip\n- Bifid nasal tip\n- Downslanted palpebral fissures\n- Telecanthus\n- Exotropia\n- Nystagmus\n- Sprengel anomaly\n- Partial agenesis of the corpus callosum\n- Split nail\n- Frontal bossing\n- Coarse hair\n- Clinodactyly of the 5th finger\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/06468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/06469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/06470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Triangular face\n- Long philtrum\n- Bulbous nose\n- Wide nasal bridge\n- Anteverted nares\n- Deeply set eye\n- Alopecia\n- Short foot\n- Downturned corners of mouth\n- Hypocalcemia\n- Hyperphosphatemia\n- Short palm\n- Depressed nasal bridge\n- External ear malformation\n- Hypomagnesiuria\n- Decreased circulating parathyroid hormone level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/06471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Triangular face\n- Long philtrum\n- Bulbous nose\n- Wide nasal bridge\n- Anteverted nares\n- Deeply set eye\n- Alopecia\n- Short foot\n- Downturned corners of mouth\n- Hypocalcemia\n- Hyperphosphatemia\n- Short palm\n- Depressed nasal bridge\n- External ear malformation\n- Hypomagnesiuria\n- Decreased circulating parathyroid hormone level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/06472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertrichosis\n- Seizure\n- Global developmental delay\n- Hip dysplasia\n- Secundum atrial septal defect\n- Constipation\n- Status epilepticus\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertrichosis\n- Seizure\n- Global developmental delay\n- Hip dysplasia\n- Secundum atrial septal defect\n- Constipation\n- Status epilepticus\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/06478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/06487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/06503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/06510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/06512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/06516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/06530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/06531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/06538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/06539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/06540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/06541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/06545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/06546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/06547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/06553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Oculomotor apraxia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Limb hypertonia\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/06554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/06556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/06557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/06558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Prominent nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Ptosis\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/06573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Brachycephaly\n- Facial asymmetry\n- Unilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/06575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/06576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/06585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/06586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06591.png"} 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most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06599.png"} 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likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06607.png"} 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diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/06613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06615.png"} 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the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/06633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06639.png"} 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diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/06655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/06662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Strabismus\n- Widely spaced teeth\n- Hypopigmentation of the skin\n- Gait ataxia\n- Sleep disturbance\n- Hypopigmentation of hair\n- Severe global developmental delay\n- Happy demeanor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Oculomotor apraxia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Limb hypertonia\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/06670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Oculomotor apraxia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Limb hypertonia\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/06671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Oculomotor apraxia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Limb hypertonia\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/06672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Oculomotor apraxia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Limb hypertonia\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/06674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Oculomotor apraxia\n- Global developmental delay\n- Cerebellar hypoplasia\n- Limb hypertonia\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/06675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Mandibular prognathia\n- Widely spaced teeth\n- Hyperreflexia\n- Cerebral cortical atrophy\n- Lumbar hyperlordosis\n- Flat occiput\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Keratoconus\n- Widely spaced teeth\n- Agitation\n- Aggressive behavior\n- Inappropriate laughter\n- Hirsutism\n- Seizure\n- Motor delay\n- Hyperreflexia\n- Truncal ataxia\n- Thoracic scoliosis\n- Short stature\n- Flat occiput\n- Protruding tongue\n- Inappropriate crying\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Widely spaced teeth\n- Inappropriate laughter\n- Hyperreflexia\n- Gait ataxia\n- Scoliosis\n- Thoracic scoliosis\n- Short stature\n- Flat occiput\n- Multiple palmar creases\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Strabismus\n- Inappropriate laughter\n- Hirsutism\n- Seizure\n- Global developmental delay\n- Hyperreflexia\n- Gait ataxia\n- Lumbar hyperlordosis\n- Thoracic scoliosis\n- Flat occiput\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Aggressive behavior\n- Inappropriate laughter\n- Hyperactivity\n- Seizure\n- Ataxia\n- Global developmental delay\n- Hyperreflexia\n- Flat occiput\n- Abnormal pyramidal sign\n- Protruding tongue\n- obsolete Toe walking\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Mandibular prognathia\n- Seizure\n- Ataxia\n- Global developmental delay\n- Absent speech\n- Truncal ataxia\n- Thoracolumbar scoliosis\n- Mild short stature\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/06723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the ureter\n- Cleft palate\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Hyperactivity\n- Tapered finger\n- Seizure\n- Choreoathetosis\n- Motor delay\n- Cerebral atrophy\n- Aganglionic megacolon\n- Intellectual disability, moderate\n- Developmental regression\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Ectopic anus\n- Cerebral hypomyelination\n- Small finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/06724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the ureter\n- Cleft palate\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Hyperactivity\n- Tapered finger\n- Seizure\n- Choreoathetosis\n- Motor delay\n- Cerebral atrophy\n- Aganglionic megacolon\n- Intellectual disability, moderate\n- Developmental regression\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Ectopic anus\n- Cerebral hypomyelination\n- Small finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/06725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Large earlobe\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/06726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Hypopigmentation of the skin\n- Generalized hypotonia\n- Dysphagia\n- Respiratory distress\n- Abnormality of speech or vocalization\n- Sleep disturbance\n- Loss of ambulation\n- Tachypnea\n- EEG with spike-wave complexes (<2.5 Hz)\n- Intellectual disability, severe\n- Alternating exotropia\n- Myoclonic seizure\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Hypopigmentation of the skin\n- Generalized hypotonia\n- Dysphagia\n- Respiratory distress\n- Abnormality of speech or vocalization\n- Sleep disturbance\n- Loss of ambulation\n- Tachypnea\n- EEG with spike-wave complexes (<2.5 Hz)\n- Intellectual disability, severe\n- Alternating exotropia\n- Myoclonic seizure\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/06822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/06829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/06836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/06846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/06847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/06852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/06853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/06857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/06866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/06874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/06875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/06877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/06878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/06879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/06880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/06881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/06882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/06883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Hearing impairment\n- Underdeveloped nasal alae\n- Oligodontia\n- Hypothyroidism\n- Severe failure to thrive\n- Exocrine pancreatic insufficiency\n- Abnormal scalp morphology\n- Steatorrhea\n- Bilateral cleft lip and palate\n- Short stature\n- Mild neurosensory hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/06895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/06904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/06910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/06911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/06912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/06913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/06914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/06915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/06916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/06920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/06921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Flexion contracture\n- Distal amyotrophy\n- Calcification of the auricular cartilage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/06922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Brachycephaly\n- Macrocephaly\n- Broad forehead\n- Hearing impairment\n- Macrotia\n- Broad nasal tip\n- Deeply set eye\n- Downslanted palpebral fissures\n- Abnormality of vision\n- Ptosis\n- Autism\n- Delayed speech and language development\n- Hypotonia\n- Thin nail\n- Truncal obesity\n- Hypoplasia of the corpus callosum\n- Sparse body hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Distal amyotrophy\n- Reduced bone mineral density\n- Elevated circulating alpha-fetoprotein concentration\n- Repetitive compulsive behavior\n- Lipodystrophy\n- Impaired glucose tolerance\n- Increased size of the mandible\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/06923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Brachycephaly\n- Macrocephaly\n- Broad forehead\n- Hearing impairment\n- Macrotia\n- Broad nasal tip\n- Deeply set eye\n- Downslanted palpebral fissures\n- Abnormality of vision\n- Ptosis\n- Autism\n- Delayed speech and language development\n- Hypotonia\n- Thin nail\n- Truncal obesity\n- Hypoplasia of the corpus callosum\n- Sparse body hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Distal amyotrophy\n- Reduced bone mineral density\n- Elevated circulating alpha-fetoprotein concentration\n- Repetitive compulsive behavior\n- Lipodystrophy\n- Impaired glucose tolerance\n- Increased size of the mandible\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/06924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Broad forehead\n- Hearing impairment\n- Macrotia\n- Deeply set eye\n- Downslanted palpebral fissures\n- Ptosis\n- Anxiety\n- Insulin-resistant diabetes mellitus\n- Intellectual disability\n- Hypotonia\n- Hip dysplasia\n- Thin nail\n- Truncal obesity\n- Sparse body hair\n- Cerebral calcification\n- Multiple joint contractures\n- Distal amyotrophy\n- Reduced bone mineral density\n- Calcification of the auricular cartilage\n- Elevated circulating alpha-fetoprotein concentration\n- Bone cyst\n- Overweight\n- Increased size of the mandible\n- Tics\n- Self-injurious behavior\n- Torus palatinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/06925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/06926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/06928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/06929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/06930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/06931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/06932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/06933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Thin vermilion border\n- Low-set, posteriorly rotated ears\n- Short neck\n- Astigmatism\n- Strabismus\n- Amblyopia\n- Dental malocclusion\n- Microdontia\n- Delayed speech and language development\n- Hypothyroidism\n- Hypertension\n- Congenital hypothyroidism\n- Brachydactyly\n- Intellectual disability\n- Small for gestational age\n- High pitched voice\n- Short foot\n- Delayed gross motor development\n- Delayed skeletal maturation\n- Kyphosis\n- Hyperuricosuria\n- Proportionate short stature\n- Severe short stature\n- Hypouricemia\n- Chronic constipation\n- Short palpebral fissure\n- Abnormal thyroid-stimulating hormone level\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/06934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/06937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/06938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/06947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/06948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/06949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/06950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/06951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/06955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/06959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/06966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/06967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/06968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/06969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/06970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/06972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/06973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/06977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Short philtrum\n- Atypical behavior\n- Brachydactyly\n- Language impairment\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/06978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Short philtrum\n- Posteriorly rotated ears\n- Broad nasal tip\n- Delayed puberty\n- Brachydactyly\n- Intellectual disability\n- Language impairment\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Premature ovarian insufficiency\n- Abnormal columella morphology\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/06979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Menorrhagia\n- Thin vermilion border\n- Short philtrum\n- Hearing impairment\n- Atypical behavior\n- Intellectual disability\n- Language impairment\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n- Broad fingertip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/06980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Short philtrum\n- Hearing impairment\n- Intellectual disability\n- Macrodontia\n- Language impairment\n- Delayed skeletal maturation\n- Short stature\n- Short 5th finger\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/06981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Short philtrum\n- Prominent nose\n- Atypical behavior\n- Broad finger\n- Language impairment\n- Clinodactyly of the 5th finger\n- Short stature\n- Low hanging columella\n- Broad fingertip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/06982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/06986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/06992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/06993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thick lower lip vermilion\n- Hearing impairment\n- Long eyelashes\n- Thick eyebrow\n- Hypertrichosis\n- Intellectual disability\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Dandy-Walker malformation\n- Cerebellar hypoplasia\n- Sparse scalp hair\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the nails\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/06999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/07005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/07006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/07007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/07008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/07009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/07010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/07011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/07012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/07013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/07018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/07019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/07023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/07024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal pinna morphology\n- Bulbous nose\n- Long nose\n- Mandibulofacial dysostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/07040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/07041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/07042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/07043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/07044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/07045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Narrow palate\n- Parietal bossing\n- Hypertelorism\n- Proptosis\n- Dental crowding\n- Multiple impacted teeth\n- Frontal bossing\n- Short stature\n- Agenesis of permanent teeth\n- Increased head circumference\n- Abnormal trabecular bone morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/07046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow palate\n- Mandibular prognathia\n- Hypertelorism\n- Abnormal maxilla morphology\n- Wide nasal bridge\n- Proptosis\n- Multiple impacted teeth\n- Frontal bossing\n- Short stature\n- Narrow jaw\n- Abnormal trabecular bone morphology\n- Abnormal mandible coronoid process morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/07047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/07048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/07053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/07056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/07057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/07058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/07059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/07060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/07061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/07062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/07063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/07064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/07112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/07113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/07116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/07125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/07127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/07128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Short neck\n- Delayed speech and language development\n- Ectopia lentis\n- Arachnodactyly\n- Seizure\n- Hypernasal speech\n- Atrial septal defect\n- Delayed skeletal maturation\n- Long nose\n- Aortic aneurysm\n- Low hanging columella\n- Gluten intolerance\n- Cutaneous syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Short neck\n- Delayed speech and language development\n- Precocious puberty\n- Hypernasal speech\n- Delayed skeletal maturation\n- Long nose\n- Clinodactyly of the 5th finger\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Short neck\n- Delayed speech and language development\n- Hypernasal speech\n- Delayed skeletal maturation\n- Long nose\n- Clinodactyly of the 5th finger\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Short neck\n- Delayed speech and language development\n- Hypernasal speech\n- Atrial septal defect\n- Delayed skeletal maturation\n- Long nose\n- Clinodactyly of the 5th finger\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Short neck\n- Delayed speech and language development\n- Hypernasal speech\n- Delayed skeletal maturation\n- Long nose\n- 2-3 toe syndactyly\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/07138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/07161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/07162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/07163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/07164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Astigmatism\n- Strabismus\n- Hypermetropia\n- Delayed speech and language development\n- Global developmental delay\n- Patent ductus arteriosus\n- Flat forehead\n- Abnormal columella morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Abnormality of the nose\n- Recurrent otitis media\n- Long eyelashes\n- Global developmental delay\n- Motor delay\n- Delayed closure of the anterior fontanelle\n- Short stature\n- Long eyebrows\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Inappropriate laughter\n- Ataxia\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Inappropriate laughter\n- Ataxia\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Inappropriate laughter\n- Ataxia\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Inappropriate laughter\n- Ataxia\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Inappropriate laughter\n- Ataxia\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Triangular face\n- Anteverted nares\n- Proptosis\n- Blue sclerae\n- Hypoplasia of teeth\n- Frontal bossing\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Triangular face\n- Anteverted nares\n- Proptosis\n- Blue sclerae\n- Hypoplasia of teeth\n- Frontal bossing\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Everted lower lip vermilion\n- Narrow face\n- Long face\n- High forehead\n- Downslanted palpebral fissures\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Accelerated skeletal maturation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Everted lower lip vermilion\n- Narrow face\n- Long face\n- High forehead\n- Downslanted palpebral fissures\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Accelerated skeletal maturation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Narrow face\n- Long face\n- High forehead\n- Atypical behavior\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Scoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Narrow face\n- Long face\n- High forehead\n- Atypical behavior\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Scoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Long philtrum\n- Anteverted nares\n- Deeply set eye\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Short nose\n- Depressed nasal bridge\n- Sparse hair\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Atypical behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Hypermetropia\n- Optic disc pallor\n- Myopia\n- Nystagmus\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Migraine\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Hypermetropia\n- Optic disc pallor\n- Myopia\n- Nystagmus\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Migraine\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Kyphoscoliosis\n- Accelerated skeletal maturation\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- EEG abnormality\n- Kyphoscoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- EEG abnormality\n- Kyphoscoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- EEG abnormality\n- Kyphoscoliosis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Optic disc pallor\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- EEG abnormality\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Optic disc pallor\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- EEG abnormality\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Facial asymmetry\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- EEG abnormality\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Facial asymmetry\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- EEG abnormality\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Facial asymmetry\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- EEG abnormality\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Facial asymmetry\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- EEG abnormality\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Everted lower lip vermilion\n- Macrocephaly\n- Narrow face\n- Long face\n- High forehead\n- Strabismus\n- Downslanted palpebral fissures\n- Nystagmus\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Ventriculomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Hypoplasia of the maxilla\n- Abnormality of the nose\n- 11 pairs of ribs\n- Brachydactyly\n- Coarctation of aorta\n- Dislocated radial head\n- Intellectual disability, borderline\n- Low hanging columella\n- Broad fingertip\n- Moderate expressive language delay\n- Radial deviation of the 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Hypoplasia of the maxilla\n- Abnormality of the nose\n- 11 pairs of ribs\n- Brachydactyly\n- Coarctation of aorta\n- Dislocated radial head\n- Intellectual disability, borderline\n- Low hanging columella\n- Broad fingertip\n- Moderate expressive language delay\n- Radial deviation of the 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Conductive hearing impairment\n- Hypermetropia\n- Carious teeth\n- Microdontia\n- Brachydactyly\n- Expressive language delay\n- Intellectual disability, borderline\n- Low hanging columella\n- Broad fingertip\n- Broad thumb\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Velopharyngeal insufficiency\n- Short philtrum\n- Triangular face\n- Hearing impairment\n- Abnormality of the nose\n- Low-set ears\n- Hip dysplasia\n- Intellectual disability, moderate\n- Low hanging columella\n- Moderate expressive language delay\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Triangular face\n- Abnormality of the nose\n- 11 pairs of ribs\n- Intellectual disability\n- Umbilical hernia\n- Expressive language delay\n- Low hanging columella\n- Ivory epiphyses of the distal phalanges of the hand\n- Congenital posterior urethral valve\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Triangular face\n- Abnormality of the nose\n- 11 pairs of ribs\n- Intellectual disability\n- Umbilical hernia\n- Expressive language delay\n- Low hanging columella\n- Ivory epiphyses of the distal phalanges of the hand\n- Congenital posterior urethral valve\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Strabismus\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Short middle phalanx of finger\n- Low hanging columella\n- Broad fingertip\n- Broad thumb\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Retrognathia\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Carious teeth\n- Microdontia\n- Brachydactyly\n- Intellectual disability, borderline\n- Low hanging columella\n- Short 1st metacarpal\n- Broad fingertip\n- Broad thumb\n- Moderate expressive language delay\n- Varicocele\n- Clinodactyly\n- Epididymal cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Brachydactyly\n- Intellectual disability, mild\n- Low hanging columella\n- Short 5th metacarpal\n- Broad fingertip\n- Broad thumb\n- Moderate expressive language delay\n- Clinodactyly\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Brachydactyly\n- Intellectual disability, mild\n- Low hanging columella\n- Short 5th metacarpal\n- Broad fingertip\n- Broad thumb\n- Moderate expressive language delay\n- Clinodactyly\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Everted lower lip vermilion\n- Long face\n- Retrognathia\n- Hearing impairment\n- Webbed neck\n- Hypermetropia\n- Upslanted palpebral fissure\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Cafe-au-lait spot\n- Hemangioma\n- Slender finger\n- Hypotonia\n- Motor delay\n- Dyscalculia\n- Unilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Epicanthus\n- Facial hypotonia\n- Long philtrum\n- Micrognathia\n- Posteriorly rotated ears\n- Bulbous nose\n- Torticollis\n- Proptosis\n- Abnormal sclera morphology\n- Hypotonia\n- Motor delay\n- Laryngomalacia\n- Gastroesophageal reflux\n- Obstructive sleep apnea\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Menorrhagia\n- Macroglossia\n- High palate\n- Hearing impairment\n- Hypermetropia\n- Microphthalmia\n- Atypical behavior\n- Autism\n- obsolete Mood swings\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Long foot\n- Sandal gap\n- Intellectual disability, moderate\n- Arthralgia\n- Elbow flexion contracture\n- Abnormal toenail morphology\n- Flat face\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Wide mouth\n- Bulbous nose\n- Convex nasal ridge\n- Periorbital fullness\n- Delayed speech and language development\n- Soft skin\n- Bruising susceptibility\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Overlapping toe\n- Expressive language delay\n- Tracheomalacia\n- Ankyloglossia\n- Abnormal CNS myelination\n- Thick vermilion border\n- Pineal cyst\n- Otitis media with effusion\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Square face\n- Bulbous nose\n- Psychosis\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Abnormal corpus callosum morphology\n- Expressive language delay\n- Abnormal aggressive, impulsive or violent behavior\n- Attention deficit hyperactivity disorder\n- Low hanging columella\n- Glue ear\n- Tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Long face\n- Facial asymmetry\n- Narrow forehead\n- Myopia\n- Dental crowding\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Pectus excavatum\n- Irregular menstruation\n- Cafe-au-lait spot\n- Intellectual disability, mild\n- Motor delay\n- Bilateral ptosis\n- Sandal gap\n- Expressive language delay\n- High, narrow palate\n- Capillary malformation\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Long face\n- Cataract\n- Myopia\n- Psychosis\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Pectus excavatum\n- Prominent fingertip pads\n- Slender finger\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Dilated cardiomyopathy\n- Constipation\n- Expressive language delay\n- Intellectual disability, severe\n- Slender toe\n- Upper eyelid edema\n- Vitamin B12 deficiency\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Long face\n- Cataract\n- Myopia\n- Psychosis\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Pectus excavatum\n- Prominent fingertip pads\n- Slender finger\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Dilated cardiomyopathy\n- Constipation\n- Expressive language delay\n- Intellectual disability, severe\n- Slender toe\n- Upper eyelid edema\n- Vitamin B12 deficiency\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Long face\n- Cataract\n- Myopia\n- Psychosis\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Pectus excavatum\n- Prominent fingertip pads\n- Slender finger\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Dilated cardiomyopathy\n- Constipation\n- Expressive language delay\n- Intellectual disability, severe\n- Slender toe\n- Upper eyelid edema\n- Vitamin B12 deficiency\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Long face\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Downslanted palpebral fissures\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Slender finger\n- Intellectual disability, mild\n- Motor delay\n- Sleep disturbance\n- Scoliosis\n- Feeding difficulties\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Long face\n- Hypertelorism\n- Long philtrum\n- High forehead\n- Downslanted palpebral fissures\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Slender finger\n- Intellectual disability, mild\n- Motor delay\n- Sleep disturbance\n- Scoliosis\n- Feeding difficulties\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- High forehead\n- Narrow nasal bridge\n- Myopia\n- Aggressive behavior\n- Short attention span\n- Delayed speech and language development\n- Pectus carinatum\n- Hypotonia\n- Intellectual disability, mild\n- Joint hypermobility\n- Slender build\n- Mitral regurgitation\n- Mutism\n- Expressive language delay\n- Large earlobe\n- Dilatation of the sinus of Valsalva\n- Long nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- High forehead\n- Narrow nasal bridge\n- Myopia\n- Aggressive behavior\n- Short attention span\n- Delayed speech and language development\n- Pectus carinatum\n- Hypotonia\n- Intellectual disability, mild\n- Joint hypermobility\n- Slender build\n- Mitral regurgitation\n- Mutism\n- Expressive language delay\n- Large earlobe\n- Dilatation of the sinus of Valsalva\n- Long nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow palate\n- Everted lower lip vermilion\n- Narrow face\n- Long face\n- Epicanthus\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- High forehead\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Large hands\n- Prominent fingertip pads\n- Seizure\n- Neonatal hypotonia\n- Long foot\n- Deep philtrum\n- Scoliosis\n- Short nose\n- Accelerated skeletal maturation\n- Bullet-shaped phalanges of the hand\n- Midface retrusion\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow palate\n- Everted lower lip vermilion\n- Narrow face\n- Long face\n- Epicanthus\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- High forehead\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Large hands\n- Prominent fingertip pads\n- Seizure\n- Neonatal hypotonia\n- Long foot\n- Deep philtrum\n- Scoliosis\n- Short nose\n- Accelerated skeletal maturation\n- Bullet-shaped phalanges of the hand\n- Midface retrusion\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Umbilical hernia\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n- Premature ventricular contraction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Patent ductus arteriosus\n- Hypoplasia of the corpus callosum\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Patent ductus arteriosus\n- Hypoplasia of the corpus callosum\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Hypoplasia of the corpus callosum\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Scoliosis\n- Kyphosis\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Abnormal heart morphology\n- Scoliosis\n- Kyphosis\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Abnormal heart morphology\n- Scoliosis\n- Kyphosis\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Scoliosis\n- Kyphosis\n- Short stature\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of skeletal maturation\n- Intellectual disability\n- Scoliosis\n- Kyphosis\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Short philtrum\n- Bulbous nose\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Wide nose\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Hypertrichosis\n- Atopic dermatitis\n- Intellectual disability\n- Motor delay\n- Clinodactyly of the 5th finger\n- Preauricular pit\n- Prominent metopic ridge\n- Low hanging columella\n- Abnormal temper tantrums\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Small scrotum\n- Hydronephrosis\n- Microcephaly\n- Hearing impairment\n- Wide nasal bridge\n- Optic atrophy\n- Intellectual disability\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Flexion contracture\n- Anteriorly placed anus\n- Talipes equinovarus\n- Ventriculomegaly\n- Aplasia\/Hypoplasia of the patella\n- Colpocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Small scrotum\n- Hydronephrosis\n- Microcephaly\n- Hearing impairment\n- Wide nasal bridge\n- Optic atrophy\n- Intellectual disability\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Flexion contracture\n- Anteriorly placed anus\n- Talipes equinovarus\n- Ventriculomegaly\n- Aplasia\/Hypoplasia of the patella\n- Colpocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Hypoplastic labia minora\n- Microcephaly\n- Prominent nasal bridge\n- Optic atrophy\n- Abnormal rib morphology\n- Intellectual disability\n- Flexion contracture\n- Anteriorly placed anus\n- Atrial septal defect\n- Talipes equinovarus\n- Abnormal patella morphology\n- Aplasia\/Hypoplasia of the patella\n- Aplasia\/Hypoplasia of the corpus callosum\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Microcephaly\n- Coarse facial features\n- Micrognathia\n- Bulbous nose\n- Broad nasal tip\n- Motor delay\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Talipes equinovarus\n- Abnormal pelvic girdle bone morphology\n- Hip contracture\n- Knee flexion contracture\n- Patellar aplasia\n- Aplasia\/Hypoplasia of the corpus callosum\n- Clitoral hypertrophy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Small scrotum\n- Hydronephrosis\n- Microcephaly\n- Coarse facial features\n- Micrognathia\n- Bulbous nose\n- Broad nasal tip\n- Motor delay\n- Atrial septal defect\n- Talipes equinovarus\n- Knee flexion contracture\n- Patellar aplasia\n- Aplasia\/Hypoplasia of the corpus callosum\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia minora\n- Microcephaly\n- Coarse facial features\n- Micrognathia\n- Bulbous nose\n- Broad nasal tip\n- Motor delay\n- Abnormal pelvic girdle bone morphology\n- Hip contracture\n- Knee flexion contracture\n- Patellar aplasia\n- Aplasia\/Hypoplasia of the corpus callosum\n- Clitoral hypertrophy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia minora\n- Microcephaly\n- Coarse facial features\n- Micrognathia\n- Bulbous nose\n- Broad nasal tip\n- Motor delay\n- Abnormal pelvic girdle bone morphology\n- Hip contracture\n- Knee flexion contracture\n- Patellar aplasia\n- Aplasia\/Hypoplasia of the corpus callosum\n- Clitoral hypertrophy\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Mask-like facies\n- Bulbous nose\n- Blepharophimosis\n- Abnormal thumb morphology\n- Hypotonia\n- Specific learning disability\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Blepharophimosis\n- Delayed speech and language development\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Blepharophimosis\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Blepharophimosis\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Blepharophimosis\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Blepharophimosis\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Hypoplastic labia minora\n- Ureteropelvic junction obstruction\n- Hydronephrosis\n- Thick lower lip vermilion\n- Narrow palate\n- High palate\n- Everted lower lip vermilion\n- Microcephaly\n- Coarse facial features\n- Epicanthus\n- Abnormality of the philtrum\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Overfolded helix\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Optic nerve hypoplasia\n- Delayed eruption of permanent teeth\n- Delayed speech and language development\n- Pectus excavatum\n- Nevus flammeus\n- Brachydactyly\n- Syndactyly\n- Hand clenching\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Anteriorly placed anus\n- Atrial septal defect\n- Patent ductus arteriosus\n- Talipes equinovarus\n- Gastroesophageal reflux\n- Curly hair\n- EEG abnormality\n- Low-set nipples\n- Tracheomalacia\n- Obstructive sleep apnea\n- Elbow flexion contracture\n- Short nose\n- Short stature\n- Knee flexion contracture\n- Patellar aplasia\n- Wide intermamillary distance\n- Aplasia\/Hypoplasia of the corpus callosum\n- Palmoplantar cutis laxa\n- Bilateral single transverse palmar creases\n- Sparse hair\n- Microtia\n- High anterior hairline\n- Abnormality of upper lip vermillion\n- Severe global developmental delay\n- Feeding difficulties\n- Wide nasal base\n- Central diaphragmatic hernia\n- Femur fracture\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia minora\n- Hydronephrosis\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Mask-like facies\n- Pointed chin\n- Smooth philtrum\n- Low-set ears\n- Bulbous nose\n- Prominent nasal bridge\n- Broad nasal tip\n- Nasolacrimal duct obstruction\n- Blepharophimosis\n- Optic nerve hypoplasia\n- Brachydactyly\n- Syndactyly\n- Hand clenching\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Atrial septal defect\n- Patent ductus arteriosus\n- Vomiting\n- Gastroesophageal reflux\n- Radioulnar synostosis\n- Clinodactyly of the 5th finger\n- Short stature\n- Knee flexion contracture\n- Patellar aplasia\n- Bilateral single transverse palmar creases\n- Feeding difficulties\n- Central diaphragmatic hernia\n- Ureterovesical junction obstruction\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Bifid uvula\n- Thin upper lip vermilion\n- Facial hypotonia\n- Pointed chin\n- Short philtrum\n- Short chin\n- Micrognathia\n- Abnormal pinna morphology\n- Small earlobe\n- Bulbous nose\n- Prominent nasal bridge\n- Long neck\n- Strabismus\n- Ptosis\n- Nasolacrimal duct obstruction\n- Delayed speech and language development\n- Glandular hypospadias\n- Short sternum\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Constipation\n- Myopathic facies\n- Expressive language delay\n- Meconium ileus\n- Prominent nasal tip\n- Wide intermamillary distance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Microcephaly\n- Mask-like facies\n- Narrow forehead\n- Low-set ears\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Bulbous nose\n- Prominent nasal bridge\n- Ptosis\n- Hypermetropia\n- Blepharophimosis\n- Hypothyroidism\n- Hypotonia\n- Absent speech\n- Polyhydramnios\n- Laryngomalacia\n- Ventricular septal defect\n- Atrial septal defect\n- Talipes equinovarus\n- Intellectual disability, profound\n- Pulmonary artery stenosis\n- Aplasia\/Hypoplasia of the corpus callosum\n- Abnormality of the palmar creases\n- Feeding difficulties\n- Profound global developmental delay\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mask-like facies\n- Micrognathia\n- Low-set ears\n- Conductive hearing impairment\n- Bulbous nose\n- Prominent nasal bridge\n- Astigmatism\n- Strabismus\n- Ptosis\n- Blepharophimosis\n- Hypoplasia of teeth\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Polyhydramnios\n- Atrial septal defect\n- Patent ductus arteriosus\n- Talipes equinovarus\n- Aspiration\n- Abnormal patella morphology\n- Increased nuchal translucency\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mask-like facies\n- Micrognathia\n- Low-set ears\n- Conductive hearing impairment\n- Bulbous nose\n- Prominent nasal bridge\n- Astigmatism\n- Strabismus\n- Ptosis\n- Blepharophimosis\n- Hypoplasia of teeth\n- Widely spaced teeth\n- Delayed speech and language development\n- Intellectual disability\n- Polyhydramnios\n- Atrial septal defect\n- Patent ductus arteriosus\n- Talipes equinovarus\n- Aspiration\n- Abnormal patella morphology\n- Increased nuchal translucency\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Microcephaly\n- Retrognathia\n- Pointed chin\n- Micrognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Strabismus\n- obsolete Sparse and thin eyebrow\n- Hypothyroidism\n- Hypotonia\n- Motor delay\n- Abnormal corpus callosum morphology\n- Absent speech\n- Flexion contracture\n- Joint hypermobility\n- Laryngomalacia\n- Gastroesophageal reflux\n- Radioulnar synostosis\n- Abnormal patella morphology\n- Lacrimal duct stenosis\n- Intellectual disability, severe\n- Severe global developmental delay\n- Oral aversion\n- Tibial torsion\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Clitoral hypoplasia\n- Hypoplastic labia minora\n- Hydronephrosis\n- Narrow mouth\n- Cleft palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Full cheeks\n- Mask-like facies\n- Pointed chin\n- Smooth philtrum\n- Short philtrum\n- Facial asymmetry\n- Short chin\n- Narrow forehead\n- Protruding ear\n- Bulbous nose\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Narrow nasal bridge\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Myopia\n- Exotropia\n- Abnormal optic nerve morphology\n- Blue sclerae\n- Abnormality of the frontal hairline\n- Long palpebral fissure\n- Abnormal dental enamel morphology\n- Delayed eruption of teeth\n- Hypoplasia of teeth\n- Microdontia\n- Delayed speech and language development\n- Hypotonia\n- Agenesis of corpus callosum\n- Dystonia\n- Absent speech\n- Abnormal heart morphology\n- Atrial septal defect\n- Talipes equinovarus\n- Short columella\n- Ventriculomegaly\n- Cortical dysplasia\n- Arthrogryposis multiplex congenita\n- Thoracolumbar scoliosis\n- Patellar aplasia\n- Absent cupid's bow\n- Intellectual disability, severe\n- Dilatation of the renal pelvis\n- Feeding difficulties\n- Ocular melanocytosis\n- Colpocephaly\n- Ulcerative colitis\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Clitoral hypoplasia\n- Hypoplastic labia minora\n- Hydronephrosis\n- Narrow mouth\n- Cleft palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Full cheeks\n- Mask-like facies\n- Pointed chin\n- Smooth philtrum\n- Short philtrum\n- Facial asymmetry\n- Short chin\n- Narrow forehead\n- Protruding ear\n- Bulbous nose\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Narrow nasal bridge\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Myopia\n- Exotropia\n- Abnormal optic nerve morphology\n- Blue sclerae\n- Abnormality of the frontal hairline\n- Long palpebral fissure\n- Abnormal dental enamel morphology\n- Delayed eruption of teeth\n- Hypoplasia of teeth\n- Microdontia\n- Delayed speech and language development\n- Hypotonia\n- Agenesis of corpus callosum\n- Dystonia\n- Absent speech\n- Abnormal heart morphology\n- Atrial septal defect\n- Talipes equinovarus\n- Short columella\n- Ventriculomegaly\n- Cortical dysplasia\n- Arthrogryposis multiplex congenita\n- Thoracolumbar scoliosis\n- Patellar aplasia\n- Absent cupid's bow\n- Intellectual disability, severe\n- Dilatation of the renal pelvis\n- Feeding difficulties\n- Ocular melanocytosis\n- Colpocephaly\n- Ulcerative colitis\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Clitoral hypoplasia\n- Hypoplastic labia minora\n- Hydronephrosis\n- Narrow mouth\n- Cleft palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Full cheeks\n- Mask-like facies\n- Pointed chin\n- Smooth philtrum\n- Short philtrum\n- Facial asymmetry\n- Short chin\n- Narrow forehead\n- Protruding ear\n- Bulbous nose\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Narrow nasal bridge\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Myopia\n- Exotropia\n- Abnormal optic nerve morphology\n- Blue sclerae\n- Abnormality of the frontal hairline\n- Long palpebral fissure\n- Abnormal dental enamel morphology\n- Delayed eruption of teeth\n- Hypoplasia of teeth\n- Microdontia\n- Delayed speech and language development\n- Hypotonia\n- Agenesis of corpus callosum\n- Dystonia\n- Absent speech\n- Abnormal heart morphology\n- Atrial septal defect\n- Talipes equinovarus\n- Short columella\n- Ventriculomegaly\n- Cortical dysplasia\n- Arthrogryposis multiplex congenita\n- Thoracolumbar scoliosis\n- Patellar aplasia\n- Absent cupid's bow\n- Intellectual disability, severe\n- Dilatation of the renal pelvis\n- Feeding difficulties\n- Ocular melanocytosis\n- Colpocephaly\n- Ulcerative colitis\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Mask-like facies\n- Facial asymmetry\n- Prominent supraorbital ridges\n- Bulbous nose\n- Prominent nasal bridge\n- Strabismus\n- Amblyopia\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Dysarthria\n- Bicuspid aortic valve\n- Pes cavus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Spastic gait\n- Clonus\n- Attention deficit hyperactivity disorder\n- Feeding difficulties\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Mask-like facies\n- Facial asymmetry\n- Prominent supraorbital ridges\n- Bulbous nose\n- Prominent nasal bridge\n- Strabismus\n- Amblyopia\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Dysarthria\n- Bicuspid aortic valve\n- Pes cavus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Spastic gait\n- Clonus\n- Attention deficit hyperactivity disorder\n- Feeding difficulties\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Mask-like facies\n- Facial asymmetry\n- Prominent supraorbital ridges\n- Bulbous nose\n- Prominent nasal bridge\n- Strabismus\n- Amblyopia\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Dysarthria\n- Bicuspid aortic valve\n- Pes cavus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Spastic gait\n- Clonus\n- Attention deficit hyperactivity disorder\n- Feeding difficulties\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Intellectual disability\n- Hypotonia\n- Kyphoscoliosis\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Hypotonia\n- Kyphoscoliosis\n- Depressed nasal bridge\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Motor delay\n- Kyphoscoliosis\n- Short nose\n- Depressed nasal bridge\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Narrow face\n- Long face\n- Epicanthus\n- Mandibular prognathia\n- High forehead\n- Downslanted palpebral fissures\n- Hypermetropia\n- Autism\n- Delayed speech and language development\n- Pectus excavatum\n- Motor delay\n- Generalized hypotonia\n- Cerebellar hypoplasia\n- Flexion contracture\n- Abnormality of the nail\n- Overlapping toe\n- Frontal bossing\n- Intellectual disability, profound\n- Limb hypertonia\n- Kyphoscoliosis\n- Long nose\n- Depressed nasal bridge\n- Parietal cortical atrophy\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Autistic behavior\n- Anxiety\n- Cerebral hemorrhage\n- Pneumonia\n- Cerebellar cyst\n- Tachypnea\n- Elevated pulmonary artery pressure\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Autistic behavior\n- Anxiety\n- Cerebral hemorrhage\n- Pneumonia\n- Cerebellar cyst\n- Tachypnea\n- Elevated pulmonary artery pressure\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Autistic behavior\n- Anxiety\n- Cerebral hemorrhage\n- Pneumonia\n- Cerebellar cyst\n- Tachypnea\n- Elevated pulmonary artery pressure\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Autistic behavior\n- Anxiety\n- Cerebral hemorrhage\n- Pneumonia\n- Cerebellar cyst\n- Tachypnea\n- Elevated pulmonary artery pressure\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Autistic behavior\n- Anxiety\n- Cerebral hemorrhage\n- Pneumonia\n- Cerebellar cyst\n- Tachypnea\n- Elevated pulmonary artery pressure\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- High palate\n- Pointed chin\n- Short chin\n- Megalocornea\n- Strabismus\n- Proptosis\n- Blue sclerae\n- Abnormality of skeletal maturation\n- Global developmental delay\n- Motor delay\n- Failure to thrive\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Short nose\n- Short stature\n- Proximal placement of thumb\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/07321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hydrocephalus\n- Microretrognathia\n- Short philtrum\n- Triangular face\n- Broad forehead\n- Hearing impairment\n- Low-set ears\n- Overfolded helix\n- Macrotia\n- Anteverted nares\n- Astigmatism\n- Proptosis\n- Myopia\n- Optic atrophy\n- Delayed speech and language development\n- Hirsutism\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Absent septum pellucidum\n- Communicating hydrocephalus\n- Joint hypermobility\n- Pes planus\n- Expressive language delay\n- Kyphosis\n- Talipes valgus\n- Depressed nasal bridge\n- Caesarian section\n- Feeding difficulties\n- Clinodactyly\n- Long fingers\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/07322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Umbilical hernia\n- Low hanging columella\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/07323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hypospadias\n- Cleft palate\n- Thin upper lip vermilion\n- Abnormality of the face\n- Short philtrum\n- Triangular face\n- Preauricular skin tag\n- Prominent nose\n- Deeply set eye\n- Long eyelashes\n- Nasolacrimal duct obstruction\n- Carious teeth\n- Microdontia\n- Delayed speech and language development\n- Hirsutism\n- Atrial septal defect\n- Patent ductus arteriosus\n- Constipation\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Abnormal toenail morphology\n- Prominent ear helix\n- Broad fingertip\n- Feeding difficulties\n- Neonatal sepsis\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Thin vermilion border\n- Short philtrum\n- Triangular face\n- Bulbous nose\n- Broad nasal tip\n- Short neck\n- Deeply set eye\n- Long eyelashes\n- Delayed speech and language development\n- Intellectual disability, borderline\n- Attention deficit hyperactivity disorder\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Bulbous nose\n- Short neck\n- Deeply set eye\n- Long eyelashes\n- Myopia\n- Hyperactivity\n- Pectus excavatum\n- Hypothyroidism\n- Intellectual disability, mild\n- Accessory spleen\n- Spina bifida\n- Hyperlordosis\n- Attention deficit hyperactivity disorder\n- Low hanging columella\n- Short 5th metacarpal\n- Varicocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Short philtrum\n- Triangular face\n- Preauricular skin tag\n- Bulbous nose\n- Deeply set eye\n- Long eyelashes\n- Delayed speech and language development\n- Intellectual disability, borderline\n- Low hanging columella\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Cleft palate\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Bulbous nose\n- Long eyelashes\n- Seizure\n- Constipation\n- Asthma\n- Low hanging columella\n- Short 5th metacarpal\n- Intellectual disability, severe\n- Central hypothyroidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Short philtrum\n- Triangular face\n- Bulbous nose\n- Deeply set eye\n- Long eyelashes\n- Intellectual disability, mild\n- Vertebral fusion\n- Low hanging columella\n- Short 2nd metacarpal\n- Short 5th metacarpal\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Long eyelashes\n- Atypical behavior\n- Intellectual disability, mild\n- Intellectual disability, moderate\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Atypical behavior\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Low-set ears\n- Widely spaced teeth\n- Microdontia\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Low-set ears\n- Widely spaced teeth\n- Microdontia\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Intellectual disability\n- Abnormal heart morphology\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Intellectual disability\n- Abnormal heart morphology\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Intellectual disability\n- Abnormal heart morphology\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Deeply set eye\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Atypical behavior\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Low hanging columella\n- Broad thumb\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Deeply set eye\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Broad thumb\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Atypical behavior\n- Brachydactyly\n- Intellectual disability\n- High pitched voice\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Atypical behavior\n- Brachydactyly\n- Intellectual disability\n- Abnormal heart morphology\n- Expressive language delay\n- Short stature\n- Low hanging columella\n- Broad thumb\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Atypical behavior\n- Brachydactyly\n- Intellectual disability\n- Abnormal heart morphology\n- Expressive language delay\n- Short stature\n- Low hanging columella\n- Broad thumb\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Long eyelashes\n- Widely spaced teeth\n- Microdontia\n- Brachydactyly\n- Intellectual disability\n- Expressive language delay\n- Delayed skeletal maturation\n- Short stature\n- Low hanging columella\n- Broad thumb\n- Abnormal gastrointestinal motility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Wide nose\n- Narrow nasal bridge\n- Deeply set eye\n- Long nose\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Sloping forehead\n- Micrognathia\n- Prominent nose\n- Deeply set eye\n- Hypotonia\n- Global developmental delay\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Hypoplasia of the corpus callosum\n- High anterior hairline\n- Lower limb pain\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Sloping forehead\n- Micrognathia\n- Prominent nose\n- Deeply set eye\n- Hypotonia\n- Global developmental delay\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Hypoplasia of the corpus callosum\n- High anterior hairline\n- Lower limb pain\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydronephrosis\n- Sloping forehead\n- Micrognathia\n- Prominent nose\n- Deeply set eye\n- Hypotonia\n- Global developmental delay\n- Growth delay\n- Ventricular septal defect\n- Atrial septal defect\n- Hypoplasia of the corpus callosum\n- High anterior hairline\n- Lower limb pain\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin vermilion border\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Low-set ears\n- Protruding ear\n- Bulbous nose\n- Prominent nose\n- Hematuria\n- Hypertension\n- Brachydactyly\n- Meningitis\n- Growth delay\n- Expressive language delay\n- Clubbing of fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/07353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydronephrosis\n- Microcephaly\n- Retrognathia\n- Narrow forehead\n- Micrognathia\n- Hearing impairment\n- Bulbous nose\n- Wide nasal bridge\n- Global developmental delay\n- Agenesis of corpus callosum\n- Atrial septal defect\n- Patent ductus arteriosus\n- Talipes equinovarus\n- Ventriculomegaly\n- Neonatal respiratory distress\n- Tricuspid regurgitation\n- Patellar aplasia\n- Feeding difficulties\n- obsolete Small scrotum\n- Cardiac conduction abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Cryptorchidism\n- Abnormality of the kidney\n- Abnormality of the genital system\n- Hydronephrosis\n- Low-set, posteriorly rotated ears\n- Cupped ear\n- Depressed nasal ridge\n- Hand polydactyly\n- Absent septum pellucidum\n- Oligohydramnios\n- Laryngomalacia\n- Abnormal heart morphology\n- Atrial septal defect\n- Cardiomegaly\n- Anal atresia\n- Leukoencephalopathy\n- Abnormality of the anus\n- Contractures of the large joints\n- Aplasia\/Hypoplasia of the corpus callosum\n- Decreased testicular size\n- Infra-orbital fold\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/07394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/07395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/07396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/07399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/07400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/07412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/07414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07420.png"} 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likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07428.png"} 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likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07436.png"} 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likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07476.png"} 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most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/07482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Strabismus\n- Global developmental delay\n- Generalized hypotonia\n- Failure to thrive\n- Limb dystonia\n- Hypsarrhythmia\n- Scoliosis\n- Sacral hypertrichosis\n- Depressed nasal bridge\n- Broad eyebrow\n- Infantile spasms\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Uterine leiomyoma\n- Hearing impairment\n- Intellectual disability\n- Dysarthria\n- Pes planus\n- Unsteady gait\n- Leukoencephalopathy\n- Anarthria\n- Falls\n- Bowel incontinence\n- Scoliosis\n- Genu valgum\n- Talipes valgus\n- Generalized tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Uterine leiomyoma\n- Hearing impairment\n- Intellectual disability\n- Dysarthria\n- Pes planus\n- Unsteady gait\n- Leukoencephalopathy\n- Anarthria\n- Falls\n- Bowel incontinence\n- Scoliosis\n- Genu valgum\n- Talipes valgus\n- Generalized tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Uterine leiomyoma\n- Hearing impairment\n- Intellectual disability\n- Dysarthria\n- Pes planus\n- Unsteady gait\n- Leukoencephalopathy\n- Anarthria\n- Falls\n- Bowel incontinence\n- Scoliosis\n- Genu valgum\n- Talipes valgus\n- Generalized tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/07582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/07583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/07584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/07585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/07586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/07587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Long eyelashes\n- Synophrys\n- Hirsutism\n- Hypotonia\n- Plagiocephaly\n- Talipes equinovarus\n- Deep philtrum\n- Highly arched eyebrow\n- Short nose\n- Mild short stature\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/07588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Microretrognathia\n- Hypertelorism\n- Sloping forehead\n- Widow's peak\n- Small earlobe\n- Wide nasal bridge\n- Depressed nasal ridge\n- Short neck\n- Tapered finger\n- Calvarial skull defect\n- Hypoplasia of the corpus callosum\n- Frontal upsweep of hair\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Sparse lateral eyebrow\n- Bilateral single transverse palmar creases\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/07589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Cleft palate\n- Open mouth\n- Dolichocephaly\n- Long face\n- Hypertelorism\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Bulbous nose\n- Broad nasal tip\n- Megalocornea\n- Upslanted palpebral fissure\n- Autism\n- Hypertrichosis\n- Global developmental delay\n- Thick nasal alae\n- Staring gaze\n- Narrow incisura width\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Macrocephaly\n- Malar flattening\n- Long face\n- Epicanthus\n- Broad forehead\n- High forehead\n- Narrow nasal ridge\n- Downslanted palpebral fissures\n- Ptosis\n- Brachydactyly\n- Intellectual disability, mild\n- Plagiocephaly\n- Congenital hip dislocation\n- Highly arched eyebrow\n- Kyphosis\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/07591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Narrow mouth\n- Macrocephaly\n- Epicanthus\n- Microretrognathia\n- Broad forehead\n- Long philtrum\n- High forehead\n- Downslanted palpebral fissures\n- Brachydactyly\n- Intellectual disability, mild\n- Plagiocephaly\n- Short nail\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Kyphosis\n- Shortening of all distal phalanges of the fingers\n- Excessive wrinkled skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/07592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Autism\n- Seizure\n- Intellectual disability, mild\n- Hallux valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/07593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Autism\n- Seizure\n- Intellectual disability, mild\n- Hallux valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/07594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Nystagmus\n- Atypical behavior\n- Autism\n- Intellectual disability, moderate\n- Scoliosis\n- Genu valgum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/07597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Nystagmus\n- Atypical behavior\n- Autism\n- Intellectual disability, moderate\n- Scoliosis\n- Genu valgum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/07598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Nystagmus\n- Atypical behavior\n- Autism\n- Intellectual disability, moderate\n- Scoliosis\n- Genu valgum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/07599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hearing impairment\n- Intellectual disability, mild\n- Pes planus\n- Sleep disturbance\n- Poor fine motor coordination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/07600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Autism\n- Abnormality of extrapyramidal motor function\n- Developmental regression\n- Language impairment\n- Chronic gastritis\n- Aplasia\/Hypoplasia of the corpus callosum\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/07601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Hypertelorism\n- Bulbous nose\n- Depressed nasal ridge\n- Short neck\n- Proptosis\n- Upslanted palpebral fissure\n- Brachydactyly\n- Short nail\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short stature\n- Mesomelic\/rhizomelic limb shortening\n- Bilateral single transverse palmar creases\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/07602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Microretrognathia\n- Posteriorly rotated ears\n- Low-set, posteriorly rotated ears\n- Depressed nasal ridge\n- Long eyelashes\n- Upslanted palpebral fissure\n- Synophrys\n- Delayed eruption of primary teeth\n- Hirsutism\n- Global developmental delay\n- Intrauterine growth retardation\n- Highly arched eyebrow\n- Short nose\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Ptosis\n- Thick eyebrow\n- Prominent umbilicus\n- Short nose\n- Depressed nasal bridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Ptosis\n- Short nose\n- Depressed nasal bridge\n- Medial flaring of the eyebrow\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Low-set ears\n- Broad nasal tip\n- Short neck\n- Proptosis\n- Thick eyebrow\n- Delayed eruption of teeth\n- Pectus excavatum\n- Short foot\n- Clinodactyly of the 5th toe\n- Frontal bossing\n- Short nose\n- Cervical C2\/C3 vertebral fusion\n- Depressed nasal bridge\n- Short distal phalanx of finger\n- Broad hallux\n- Broad thumb\n- Chin with horizontal crease\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- High forehead\n- Low-set ears\n- Broad nasal tip\n- Ptosis\n- Myopia\n- Thick eyebrow\n- Amblyopia\n- Short ribs\n- Precocious puberty\n- Prominent umbilicus\n- Highly arched eyebrow\n- Short nose\n- Depressed nasal bridge\n- Accelerated skeletal maturation\n- Broad hallux\n- Broad eyebrow\n- Chin with horizontal crease\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the uterus\n- High palate\n- Thin upper lip vermilion\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Thick eyebrow\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- High palate\n- Thin upper lip vermilion\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Ptosis\n- Thick eyebrow\n- Delayed eruption of teeth\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Bifid scrotum\n- Bifid uvula\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Thick eyebrow\n- Short nose\n- Depressed nasal bridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Thick eyebrow\n- Short nose\n- Depressed nasal bridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- High palate\n- Thin upper lip vermilion\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Thick eyebrow\n- Delayed eruption of teeth\n- Natal tooth\n- Short nose\n- Chin with horizontal crease\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid scrotum\n- High palate\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Thick eyebrow\n- Short nose\n- Depressed nasal bridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/07620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Protruding ear\n- Anteverted nares\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Abnormal aggressive, impulsive or violent behavior\n- Hair-pulling\n- Self-biting\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/07626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Eczema\n- Hypotonia\n- Gait disturbance\n- Impaired mastication\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/07627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Ptosis\n- Thick eyebrow\n- Prominent umbilicus\n- Short nose\n- Depressed nasal bridge\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Wide anterior fontanel\n- Hypertelorism\n- Short chin\n- Broad forehead\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Thick eyebrow\n- Atypical behavior\n- Delayed speech and language development\n- Umbilical hernia\n- Expressive language delay\n- Short nose\n- Depressed nasal bridge\n- Short thumb\n- Long toe\n- Broad eyebrow\n- Broad thumb\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/07629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Hirsutism\n- Global developmental delay\n- Asymmetry of the ears\n- Broad chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/07655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal joint morphology\n- Abnormal mitral valve morphology\n- Intellectual disability, moderate\n- Disproportionate short stature\n- Corneal opacity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Anteverted nares\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short attention span\n- Obesity\n- Short stature\n- Feeding difficulties\n- obsolete Psychomotor retardation\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/07659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachydactyly\n- Tetralogy of Fallot\n- Intellectual disability, moderate\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypotonia\n- Intellectual disability, mild\n- Partial agenesis of the corpus callosum\n- Obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/07670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Microcephaly\n- Optic atrophy\n- Hypertension\n- Ataxia\n- Intellectual disability, mild\n- Cerebellar atrophy\n- Weight loss\n- Enlarged cisterna magna\n- Short stature\n- Aplasia\/Hypoplasia of the cerebellar vermis\n- Chronic axonal neuropathy\n- Congenital sensorineural hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/07671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Microcephaly\n- Optic atrophy\n- Hypertension\n- Ataxia\n- Intellectual disability, mild\n- Cerebellar atrophy\n- Weight loss\n- Enlarged cisterna magna\n- Short stature\n- Aplasia\/Hypoplasia of the cerebellar vermis\n- Chronic axonal neuropathy\n- Congenital sensorineural hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/07672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Strabismus\n- Nystagmus\n- Amblyopia\n- Intellectual disability, mild\n- Hypernasal speech\n- EEG abnormality\n- Language impairment\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/07673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Microcephaly\n- Mandibular prognathia\n- Strabismus\n- Myopia\n- Atypical behavior\n- Intellectual disability\n- Abnormal facial shape\n- Language impairment\n- Short stature\n- Severe expressive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/07679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Cleft upper lip\n- Hearing impairment\n- Blindness\n- Atypical behavior\n- Autism\n- Intellectual disability\n- Seizure\n- Abnormal facial shape\n- Hiatus hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/07680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Carious teeth\n- Autistic behavior\n- Delayed speech and language development\n- Global developmental delay\n- Generalized hypotonia\n- Abnormal scalp morphology\n- Echolalia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/07681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Long philtrum\n- Macrodontia of permanent maxillary central incisor\n- Intellectual disability\n- Joint stiffness\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/07683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Chorioretinal coloboma\n- Autistic behavior\n- Intellectual disability\n- Autoimmune thrombocytopenia\n- Short stature\n- Cleft vertebral arch\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Intellectual disability, mild\n- Global developmental delay\n- Intestinal malrotation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/07685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Episodic vomiting\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Sparse hair\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Brachydactyly\n- Delayed ossification of carpal bones\n- Intellectual disability\n- Hypotonia\n- Absent speech\n- Small nail\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Moderate sensorineural hearing impairment\n- Short distal phalanx of finger\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Smooth philtrum\n- Strabismus\n- Ptosis\n- Aggressive behavior\n- Delayed speech and language development\n- Hypotonia\n- Tremor\n- Mitral regurgitation\n- Pes cavus\n- Pes planus\n- Gait ataxia\n- Delayed gross motor development\n- Drooling\n- Incomprehensible speech\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Enlarged posterior fossa\n- Gait instability, worse in the dark\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Uplifted earlobe\n- Intellectual disability, severe\n- Impulsivity\n- Self-injurious behavior\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Smooth philtrum\n- Strabismus\n- Ptosis\n- Aggressive behavior\n- Delayed speech and language development\n- Hypotonia\n- Tremor\n- Mitral regurgitation\n- Pes cavus\n- Pes planus\n- Gait ataxia\n- Delayed gross motor development\n- Drooling\n- Incomprehensible speech\n- Clinodactyly of the 5th finger\n- Prominent nasal tip\n- Enlarged posterior fossa\n- Gait instability, worse in the dark\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Uplifted earlobe\n- Intellectual disability, severe\n- Impulsivity\n- Self-injurious behavior\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Dolichocephaly\n- Epicanthus\n- Full cheeks\n- Hypertelorism\n- Narrow forehead\n- Protruding ear\n- Prominent nasal bridge\n- Long eyelashes\n- Thick eyebrow\n- Hand clenching\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Small nail\n- Frontal bossing\n- Sparse scalp hair\n- 2-3 toe syndactyly\n- Prominent nasal tip\n- Prominent metopic ridge\n- Feeding difficulties in infancy\n- High anterior hairline\n- Prominent tragus\n- Cutaneous syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Bowel incontinence\n- Multifocal epileptiform discharges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/07704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Delayed speech and language development\n- Spasticity\n- Gait imbalance\n- Motor deterioration\n- Intellectual disability, moderate\n- Loss of speech\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/07705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Myopia\n- Motor delay\n- Epiphyseal dysplasia\n- Genu valgum\n- Talipes valgus\n- Infantile muscular hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/07706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormality of the chin\n- Thick eyebrow\n- Intellectual disability\n- Hypotonia\n- Joint laxity\n- Failure to thrive\n- Prominent glabella\n- High, narrow palate\n- Short stature\n- Knee dislocation\n- High anterior hairline\n- Feeding difficulties\n- Chronic constipation\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Bulbous nose\n- Broad nasal tip\n- Hypermetropia\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Global developmental delay\n- Failure to thrive\n- Gastroesophageal reflux\n- Depressed nasal bridge\n- Midface retrusion\n- Feeding difficulties\n- Chronic constipation\n- Food intolerance\n- Auditory sensitivity\n- Hip subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Epicanthus\n- Short philtrum\n- Low-set ears\n- Bulbous nose\n- Prominent nasal bridge\n- Downslanted palpebral fissures\n- Microdontia\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Low frustration tolerance\n- Reduced eye contact\n- Eczema\n- Cutis marmorata\n- Seizure\n- Global developmental delay\n- Joint hypermobility\n- Joint laxity\n- Hypsarrhythmia\n- Highly arched eyebrow\n- Thoracic scoliosis\n- Somatic sensory dysfunction\n- Prominent nasal tip\n- Prominent metopic ridge\n- High hypermetropia\n- Interictal epileptiform activity\n- Feeding difficulties\n- Chronic constipation\n- Infantile spasms\n- Narrow palpebral fissure\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hyperactivity\n- Macrodontia\n- Poor motor coordination\n- Lumbar scoliosis\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Mild global developmental delay\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Ptosis\n- Proptosis\n- Bruising susceptibility\n- Pulmonic stenosis\n- Abnormal EKG\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Ptosis\n- Pectus carinatum\n- Thin skin\n- Short stature\n- Excessive wrinkling of palmar skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Brachycephaly\n- Epicanthus\n- Low anterior hairline\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Wide nasal bridge\n- Visual impairment\n- Upslanted palpebral fissure\n- Microdontia\n- Diastema\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Umbilical hernia\n- Recurrent aspiration pneumonia\n- Apnea\n- Frontal upsweep of hair\n- Recurrent infections\n- Short stature\n- Severe muscular hypotonia\n- Impaired pain sensation\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Delayed myelination\n- Nocturnal seizures\n- Tube feeding\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/07713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Large fontanelles\n- Microcephaly\n- Coarse facial features\n- Smooth philtrum\n- Narrow forehead\n- Long philtrum\n- Low-set ears\n- Conductive hearing impairment\n- Broad nasal tip\n- Anteverted nares\n- Astigmatism\n- Long eyelashes\n- Optic disc pallor\n- Myopia\n- Thick eyebrow\n- Optic disc coloboma\n- Synophrys\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Sensory neuropathy\n- Cutis marmorata\n- Hirsutism\n- Seizure\n- Motor delay\n- Cerebellar atrophy\n- Generalized hypotonia\n- Dystonia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Ventricular septal defect\n- Hypertrophic cardiomyopathy\n- Accessory spleen\n- Pes planus\n- Deep philtrum\n- Ventriculomegaly\n- Unsteady gait\n- Highly arched eyebrow\n- Wormian bones\n- Scoliosis\n- Delayed skeletal maturation\n- Thoracic kyphosis\n- Short stature\n- Decreased body weight\n- Deep palmar crease\n- Hypoplasia of the frontal lobes\n- Axial hypotonia\n- Fetal pyelectasis\n- Severe global developmental delay\n- Midface retrusion\n- Thick vermilion border\n- Self-injurious behavior\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Large fontanelles\n- Microcephaly\n- Coarse facial features\n- Smooth philtrum\n- Narrow forehead\n- Long philtrum\n- Low-set ears\n- Conductive hearing impairment\n- Broad nasal tip\n- Anteverted nares\n- Astigmatism\n- Long eyelashes\n- Optic disc pallor\n- Myopia\n- Thick eyebrow\n- Optic disc coloboma\n- Synophrys\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Sensory neuropathy\n- Cutis marmorata\n- Hirsutism\n- Seizure\n- Motor delay\n- Cerebellar atrophy\n- Generalized hypotonia\n- Dystonia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Ventricular septal defect\n- Hypertrophic cardiomyopathy\n- Accessory spleen\n- Pes planus\n- Deep philtrum\n- Ventriculomegaly\n- Unsteady gait\n- Highly arched eyebrow\n- Wormian bones\n- Scoliosis\n- Delayed skeletal maturation\n- Thoracic kyphosis\n- Short stature\n- Decreased body weight\n- Deep palmar crease\n- Hypoplasia of the frontal lobes\n- Axial hypotonia\n- Fetal pyelectasis\n- Severe global developmental delay\n- Midface retrusion\n- Thick vermilion border\n- Self-injurious behavior\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Long face\n- Pointed chin\n- Short philtrum\n- Low-set ears\n- Strabismus\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Slurred speech\n- Joint hypermobility\n- Failure to thrive\n- Dysphagia\n- Hypothermia\n- Recurrent infections\n- Excessive salivation\n- Short stature\n- Decreased body weight\n- Chronic gastritis\n- Flat occiput\n- Widely-spaced incisors\n- Impaired pain sensation\n- High hypermetropia\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/07716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Long face\n- Pointed chin\n- Short philtrum\n- Low-set ears\n- Strabismus\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Slurred speech\n- Joint hypermobility\n- Failure to thrive\n- Dysphagia\n- Hypothermia\n- Recurrent infections\n- Excessive salivation\n- Short stature\n- Decreased body weight\n- Chronic gastritis\n- Flat occiput\n- Widely-spaced incisors\n- Impaired pain sensation\n- High hypermetropia\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/07717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Long face\n- Pointed chin\n- Short philtrum\n- Low-set ears\n- Strabismus\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Slurred speech\n- Joint hypermobility\n- Failure to thrive\n- Dysphagia\n- Hypothermia\n- Recurrent infections\n- Excessive salivation\n- Short stature\n- Decreased body weight\n- Chronic gastritis\n- Flat occiput\n- Widely-spaced incisors\n- Impaired pain sensation\n- High hypermetropia\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/07718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/07719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/07739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- High palate\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Epicanthus\n- Facial hypotonia\n- Pointed chin\n- Short philtrum\n- Low-set ears\n- Prominent nose\n- Hypermetropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Slurred speech\n- Unsteady gait\n- Intellectual disability, moderate\n- Excessive salivation\n- Impaired pain sensation\n- Axial hypotonia\n- Tented upper lip vermilion\n- Overweight\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/07740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Pointed chin\n- Hypertelorism\n- Long philtrum\n- Prominent nose\n- Broad nasal tip\n- Hypermetropia\n- Microdontia\n- Autistic behavior\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Myopathic facies\n- Abnormality of speech or vocalization\n- Unsteady gait\n- Long nose\n- Excessive salivation\n- Multiple cafe-au-lait spots\n- Narrow palpebral fissure\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/07741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Long philtrum\n- Prominent nose\n- Hypodontia\n- Abnormal dental enamel morphology\n- Tapered finger\n- Intellectual disability\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Chronic diarrhea\n- Abnormality of speech or vocalization\n- Recurrent infections\n- Low hanging columella\n- Thin lower lip vermilion\n- Narrow palpebral fissure\n- Thin eyebrow\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/07742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Intellectual disability\n- Motor delay\n- Myopathic facies\n- Abnormality of speech or vocalization\n- Hypsarrhythmia\n- Secondary microcephaly\n- Medullary nephrocalcinosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/07743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Hypertelorism\n- Short philtrum\n- Micrognathia\n- Posteriorly rotated ears\n- Prominent nose\n- Anteverted nares\n- Upslanted palpebral fissure\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Abnormal foot morphology\n- Toe syndactyly\n- Gastroesophageal reflux\n- Pyloric stenosis\n- Myopathic facies\n- Asthma\n- Abnormality of speech or vocalization\n- Downturned corners of mouth\n- Aspiration\n- Finger syndactyly\n- Sleep apnea\n- Severe global developmental delay\n- Gastrostomy tube feeding in infancy\n- Midface retrusion\n- Feeding difficulties\n- Allergy\n- Bitemporal hollowing\n- Abnormally low T cell receptor excision circle level\n- Eosinophilic dermal infiltration\n- Narrow palpebral fissure\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/07744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Pointed chin\n- Prominent nose\n- Broad nasal tip\n- Myopia\n- Upslanted palpebral fissure\n- Microdontia\n- Asthma\n- Abnormality of speech or vocalization\n- Intellectual disability, moderate\n- Recurrent infections\n- Hyperglycemia\n- Short stature\n- Maturity-onset diabetes of the young\n- Bronchiolitis\n- Allergy\n- Stuttering\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/07745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Long face\n- Pointed chin\n- Prominent nose\n- Broad nasal tip\n- Myopia\n- Upslanted palpebral fissure\n- Microdontia\n- Asthma\n- Abnormality of speech or vocalization\n- Intellectual disability, moderate\n- Recurrent infections\n- Hyperglycemia\n- Short stature\n- Maturity-onset diabetes of the young\n- Bronchiolitis\n- Allergy\n- Stuttering\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/07746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Broad philtrum\n- Facial hypotonia\n- Macrotia\n- Protruding ear\n- Long palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/07747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Long face\n- Abnormal pinna morphology\n- Macrotia\n- Autism\n- Delayed speech and language development\n- Hyperactivity\n- Single transverse palmar crease\n- Hyperextensibility of the finger joints\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Joint hypermobility\n- Pes planus\n- Drooling\n- Unsteady gait\n- Tip-toe gait\n- Tooth abscess\n- Cutaneous abscess\n- Impaired tandem gait\n- Increased size of the mandible\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/07748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Depressed nasal tip\n- Broad nasal tip\n- Short neck\n- Myopia\n- Aggressive behavior\n- Global developmental delay\n- Generalized hypotonia\n- Joint laxity\n- Obesity\n- Broad-based gait\n- Sleep disturbance\n- Waddling gait\n- Downturned corners of mouth\n- Obstructive sleep apnea\n- Overfolding of the superior helices\n- Midface retrusion\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/07749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Webbed neck\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Visual impairment\n- Impaired social interactions\n- Congenital diaphragmatic hernia\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Wormian bones\n- Downturned corners of mouth\n- Short stature\n- Depressed nasal bridge\n- Poor fine motor coordination\n- Sparse hair\n- Hypoplastic cervical vertebrae\n- Moderate expressive language delay\n- Delayed myelination\n- Impairment of activities of daily living\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bifid uvula\n- Thin vermilion border\n- Malar flattening\n- Short philtrum\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Hypermetropia\n- Atypical behavior\n- Brachydactyly\n- Abnormal thumb morphology\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Widely-spaced maxillary central incisors\n- Atrial septal defect\n- Broad foot\n- Abnormal toe morphology\n- Poor suck\n- Focal impaired awareness seizure\n- Downturned corners of mouth\n- Motor tics\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Cleft palate\n- High palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Broad forehead\n- Micrognathia\n- Hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Exotropia\n- Optic nerve hypoplasia\n- Brachydactyly\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Atrial septal defect\n- Patent foramen ovale\n- Ventriculomegaly\n- Abnormal cerebral white matter morphology\n- Downturned corners of mouth\n- Immunodeficiency\n- Short palm\n- Short stature\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Cleft palate\n- High palate\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Broad forehead\n- Micrognathia\n- Hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Exotropia\n- Optic nerve hypoplasia\n- Brachydactyly\n- Hypotonia\n- Global developmental delay\n- Dandy-Walker malformation\n- Atrial septal defect\n- Patent foramen ovale\n- Ventriculomegaly\n- Abnormal cerebral white matter morphology\n- Downturned corners of mouth\n- Immunodeficiency\n- Short palm\n- Short stature\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Protruding ear\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/07754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Protruding ear\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/07755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Protruding ear\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/07756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Gingivitis\n- Dolichocephaly\n- Long face\n- Mandibular prognathia\n- Facial asymmetry\n- Hearing impairment\n- Macrotia\n- Abnormality of refraction\n- Taurodontia\n- Seizure\n- Hypotonia\n- Joint laxity\n- Macrodontia\n- Language impairment\n- Scoliosis\n- Abnormality of dental eruption\n- Abnormal dental root morphology\n- Mesiodens\n- Central nervous system cyst\n- Anteverted ears\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/07757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bifid uvula\n- Microcephaly\n- Epicanthus\n- Mandibular prognathia\n- Strabismus\n- Nystagmus\n- Autistic behavior\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Neonatal hypotonia\n- Constipation\n- Gastroesophageal reflux\n- Sleep disturbance\n- Feeding difficulties in infancy\n- Tented upper lip vermilion\n- Flat face\n- Short palpebral fissure\n- Bifid ureter\n- Central nervous system cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertrichosis\n- Polyhydramnios\n- Patent ductus arteriosus\n- Pericardial effusion\n- Male infertility\n- Infantile muscular hypotonia\n- Cutis gyrata of scalp\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/07759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Intellectual disability\n- Pes planus\n- Obstructive sleep apnea\n- Talipes valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/07760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Narrow forehead\n- Low-set ears\n- Short neck\n- Thickened nuchal skin fold\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Proptosis\n- Hypotonia\n- Pulmonic stenosis\n- Frontal bossing\n- Ventricular septal hypertrophy\n- Feeding difficulties\n- Tube feeding\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Narrow forehead\n- Low-set ears\n- Short neck\n- Thickened nuchal skin fold\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Proptosis\n- Hypotonia\n- Pulmonic stenosis\n- Frontal bossing\n- Ventricular septal hypertrophy\n- Feeding difficulties\n- Tube feeding\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Overfolded helix\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Thick eyebrow\n- Delayed speech and language development\n- Soft skin\n- Hemangioma\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Growth delay\n- Ventricular septal defect\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Right ventricular hypertrophy\n- Deep plantar creases\n- Neonatal hypoglycemia\n- Gastroesophageal reflux\n- Apnea\n- Short stature\n- Malnutrition\n- Deep palmar crease\n- Impaired smooth pursuit\n- Sparse hair\n- Feeding difficulties\n- Sparse eyebrow\n- Premature closure of the ductus arteriosus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Short chin\n- Posteriorly rotated ears\n- Otitis media\n- Downslanted palpebral fissures\n- Corneal scarring\n- Keratoconus\n- Exotropia\n- Blindness\n- Widely spaced teeth\n- Compulsive behaviors\n- Impaired social interactions\n- Delayed speech and language development\n- Hyperactivity\n- Hypertension\n- Cutis marmorata\n- Mottled pigmentation\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Myoclonus\n- Hip dysplasia\n- Failure to thrive in infancy\n- Pes planus\n- Short foot\n- Poor suck\n- Dilated fourth ventricle\n- Coarse hair\n- Poor motor coordination\n- Drooling\n- Episodic vomiting\n- Episodic abdominal pain\n- Kyphosis\n- Hyperlordosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Flat occiput\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Infantile axial hypotonia\n- Intellectual disability, severe\n- Monocular strabismus\n- High myopia\n- Severe global developmental delay\n- Ankle clonus\n- Chronic constipation\n- Wide nasal base\n- Heart murmur\n- Choking episodes\n- Increased size of nasopharyngeal adenoids\n- Tics\n- Phonic tics\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Full cheeks\n- Low-set ears\n- Long eyelashes\n- Aggressive behavior\n- Irritability\n- Delayed speech and language development\n- Hyperactivity\n- Pectus excavatum\n- Sacral dimple\n- Urticaria\n- Mottled pigmentation\n- Prominent fingertip pads\n- Hypotonia\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Craniosynostosis\n- Prolonged QT interval\n- Gastroesophageal reflux\n- Gait imbalance\n- Delayed CNS myelination\n- Drooling\n- Unsteady gait\n- Abnormal periventricular white matter morphology\n- Bowel incontinence\n- Elevated circulating alkaline phosphatase concentration\n- Neonatal hyperbilirubinemia\n- Feeding difficulties in infancy\n- Intellectual disability, severe\n- Self-biting\n- Snout reflex\n- Systolic heart murmur\n- Decreased body fat percentage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Prominent nose\n- Long eyelashes\n- Dry skin\n- Global developmental delay\n- Motor delay\n- Pes cavus\n- Dysphagia\n- Cerebral atrophy\n- Gait imbalance\n- Intellectual disability, moderate\n- Frequent falls\n- Expressive language delay\n- Short femur\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Prominent nose\n- Long eyelashes\n- Dry skin\n- Global developmental delay\n- Motor delay\n- Pes cavus\n- Dysphagia\n- Cerebral atrophy\n- Gait imbalance\n- Intellectual disability, moderate\n- Frequent falls\n- Expressive language delay\n- Short femur\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Malar flattening\n- Long philtrum\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Aggressive behavior\n- Autistic behavior\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Attention deficit hyperactivity disorder\n- Delayed fine motor development\n- Laterally extended eyebrow\n- Clonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Coarse facial features\n- Short chin\n- Delayed speech and language development\n- Abnormal skull morphology\n- Ataxia\n- Motor delay\n- Barrel-shaped chest\n- Cardiomyopathy\n- Tachycardia\n- Prolonged QT interval\n- Medulloblastoma\n- Periventricular leukomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Short chin\n- Posteriorly rotated ears\n- Otitis media\n- Downslanted palpebral fissures\n- Corneal scarring\n- Keratoconus\n- Exotropia\n- Blindness\n- Widely spaced teeth\n- Compulsive behaviors\n- Impaired social interactions\n- Delayed speech and language development\n- Hyperactivity\n- Hypertension\n- Cutis marmorata\n- Mottled pigmentation\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Myoclonus\n- Hip dysplasia\n- Failure to thrive in infancy\n- Pes planus\n- Short foot\n- Poor suck\n- Dilated fourth ventricle\n- Coarse hair\n- Poor motor coordination\n- Drooling\n- Episodic vomiting\n- Episodic abdominal pain\n- Kyphosis\n- Hyperlordosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Flat occiput\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Infantile axial hypotonia\n- Intellectual disability, severe\n- Monocular strabismus\n- High myopia\n- Severe global developmental delay\n- Ankle clonus\n- Chronic constipation\n- Wide nasal base\n- Heart murmur\n- Choking episodes\n- Increased size of nasopharyngeal adenoids\n- Tics\n- Phonic tics\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Short chin\n- Posteriorly rotated ears\n- Otitis media\n- Downslanted palpebral fissures\n- Corneal scarring\n- Keratoconus\n- Exotropia\n- Blindness\n- Widely spaced teeth\n- Compulsive behaviors\n- Impaired social interactions\n- Delayed speech and language development\n- Hyperactivity\n- Hypertension\n- Cutis marmorata\n- Mottled pigmentation\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Myoclonus\n- Hip dysplasia\n- Failure to thrive in infancy\n- Pes planus\n- Short foot\n- Poor suck\n- Dilated fourth ventricle\n- Coarse hair\n- Poor motor coordination\n- Drooling\n- Episodic vomiting\n- Episodic abdominal pain\n- Kyphosis\n- Hyperlordosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Flat occiput\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Infantile axial hypotonia\n- Intellectual disability, severe\n- Monocular strabismus\n- High myopia\n- Severe global developmental delay\n- Ankle clonus\n- Chronic constipation\n- Wide nasal base\n- Heart murmur\n- Choking episodes\n- Increased size of nasopharyngeal adenoids\n- Tics\n- Phonic tics\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Short chin\n- Posteriorly rotated ears\n- Otitis media\n- Downslanted palpebral fissures\n- Corneal scarring\n- Keratoconus\n- Exotropia\n- Blindness\n- Widely spaced teeth\n- Compulsive behaviors\n- Impaired social interactions\n- Delayed speech and language development\n- Hyperactivity\n- Hypertension\n- Cutis marmorata\n- Mottled pigmentation\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Myoclonus\n- Hip dysplasia\n- Failure to thrive in infancy\n- Pes planus\n- Short foot\n- Poor suck\n- Dilated fourth ventricle\n- Coarse hair\n- Poor motor coordination\n- Drooling\n- Episodic vomiting\n- Episodic abdominal pain\n- Kyphosis\n- Hyperlordosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Flat occiput\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Infantile axial hypotonia\n- Intellectual disability, severe\n- Monocular strabismus\n- High myopia\n- Severe global developmental delay\n- Ankle clonus\n- Chronic constipation\n- Wide nasal base\n- Heart murmur\n- Choking episodes\n- Increased size of nasopharyngeal adenoids\n- Tics\n- Phonic tics\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Short chin\n- Posteriorly rotated ears\n- Otitis media\n- Downslanted palpebral fissures\n- Corneal scarring\n- Keratoconus\n- Exotropia\n- Blindness\n- Widely spaced teeth\n- Compulsive behaviors\n- Impaired social interactions\n- Delayed speech and language development\n- Hyperactivity\n- Hypertension\n- Cutis marmorata\n- Mottled pigmentation\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Myoclonus\n- Hip dysplasia\n- Failure to thrive in infancy\n- Pes planus\n- Short foot\n- Poor suck\n- Dilated fourth ventricle\n- Coarse hair\n- Poor motor coordination\n- Drooling\n- Episodic vomiting\n- Episodic abdominal pain\n- Kyphosis\n- Hyperlordosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Flat occiput\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Infantile axial hypotonia\n- Intellectual disability, severe\n- Monocular strabismus\n- High myopia\n- Severe global developmental delay\n- Ankle clonus\n- Chronic constipation\n- Wide nasal base\n- Heart murmur\n- Choking episodes\n- Increased size of nasopharyngeal adenoids\n- Tics\n- Phonic tics\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sinusitis\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Short chin\n- Posteriorly rotated ears\n- Otitis media\n- Downslanted palpebral fissures\n- Corneal scarring\n- Keratoconus\n- Exotropia\n- Blindness\n- Widely spaced teeth\n- Compulsive behaviors\n- Impaired social interactions\n- Delayed speech and language development\n- Hyperactivity\n- Hypertension\n- Cutis marmorata\n- Mottled pigmentation\n- Motor delay\n- Gait disturbance\n- Neonatal hypotonia\n- Myoclonus\n- Hip dysplasia\n- Failure to thrive in infancy\n- Pes planus\n- Short foot\n- Poor suck\n- Dilated fourth ventricle\n- Coarse hair\n- Poor motor coordination\n- Drooling\n- Episodic vomiting\n- Episodic abdominal pain\n- Kyphosis\n- Hyperlordosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Flat occiput\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Infantile axial hypotonia\n- Intellectual disability, severe\n- Monocular strabismus\n- High myopia\n- Severe global developmental delay\n- Ankle clonus\n- Chronic constipation\n- Wide nasal base\n- Heart murmur\n- Choking episodes\n- Increased size of nasopharyngeal adenoids\n- Tics\n- Phonic tics\n- Impulsivity\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Protruding ear\n- Multiple cafe-au-lait spots\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/07829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Short neck\n- Thick eyebrow\n- Carious teeth\n- Taurodontia\n- Pectus carinatum\n- Abnormality of the skeletal system\n- Dysostosis multiplex\n- Spasticity\n- Global developmental delay\n- Hyperreflexia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Umbilical hernia\n- Secundum atrial septal defect\n- Cardiac arrest\n- Talipes equinovarus\n- Hydrops fetalis\n- Ventriculomegaly\n- Clonus\n- Spinal cord compression\n- Recurrent respiratory infections\n- Hepatomegaly\n- Kyphosis\n- Obstructive sleep apnea\n- Elbow flexion contracture\n- Distal amyotrophy\n- Decreased body weight\n- Cervical platyspondyly\n- Basilar impression\n- Enamel hypoplasia\n- Loss of ability to walk in first decade\n- Focal white matter lesions\n- Mandibular condyle hypoplasia\n- Anterior open-bite malocclusion\n- Abnormality of permanent molar morphology\n- Abnormal aortic valve cusp morphology\n- Abnormal thoracic spine morphology\n- Abnormal lumbar spine morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Short neck\n- Thick eyebrow\n- Carious teeth\n- Taurodontia\n- Pectus carinatum\n- Abnormality of the skeletal system\n- Dysostosis multiplex\n- Spasticity\n- Global developmental delay\n- Hyperreflexia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Umbilical hernia\n- Secundum atrial septal defect\n- Cardiac arrest\n- Talipes equinovarus\n- Hydrops fetalis\n- Ventriculomegaly\n- Clonus\n- Spinal cord compression\n- Recurrent respiratory infections\n- Hepatomegaly\n- Kyphosis\n- Obstructive sleep apnea\n- Elbow flexion contracture\n- Distal amyotrophy\n- Decreased body weight\n- Cervical platyspondyly\n- Basilar impression\n- Enamel hypoplasia\n- Loss of ability to walk in first decade\n- Focal white matter lesions\n- Mandibular condyle hypoplasia\n- Anterior open-bite malocclusion\n- Abnormality of permanent molar morphology\n- Abnormal aortic valve cusp morphology\n- Abnormal thoracic spine morphology\n- Abnormal lumbar spine morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Short neck\n- Thick eyebrow\n- Carious teeth\n- Taurodontia\n- Pectus carinatum\n- Abnormality of the skeletal system\n- Dysostosis multiplex\n- Spasticity\n- Global developmental delay\n- Hyperreflexia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Umbilical hernia\n- Secundum atrial septal defect\n- Cardiac arrest\n- Talipes equinovarus\n- Hydrops fetalis\n- Ventriculomegaly\n- Clonus\n- Spinal cord compression\n- Recurrent respiratory infections\n- Hepatomegaly\n- Kyphosis\n- Obstructive sleep apnea\n- Elbow flexion contracture\n- Distal amyotrophy\n- Decreased body weight\n- Cervical platyspondyly\n- Basilar impression\n- Enamel hypoplasia\n- Loss of ability to walk in first decade\n- Focal white matter lesions\n- Mandibular condyle hypoplasia\n- Anterior open-bite malocclusion\n- Abnormality of permanent molar morphology\n- Abnormal aortic valve cusp morphology\n- Abnormal thoracic spine morphology\n- Abnormal lumbar spine morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Short neck\n- Thick eyebrow\n- Carious teeth\n- Taurodontia\n- Pectus carinatum\n- Abnormality of the skeletal system\n- Dysostosis multiplex\n- Spasticity\n- Global developmental delay\n- Hyperreflexia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Umbilical hernia\n- Secundum atrial septal defect\n- Cardiac arrest\n- Talipes equinovarus\n- Hydrops fetalis\n- Ventriculomegaly\n- Clonus\n- Spinal cord compression\n- Recurrent respiratory infections\n- Hepatomegaly\n- Kyphosis\n- Obstructive sleep apnea\n- Elbow flexion contracture\n- Distal amyotrophy\n- Decreased body weight\n- Cervical platyspondyly\n- Basilar impression\n- Enamel hypoplasia\n- Loss of ability to walk in first decade\n- Focal white matter lesions\n- Mandibular condyle hypoplasia\n- Anterior open-bite malocclusion\n- Abnormality of permanent molar morphology\n- Abnormal aortic valve cusp morphology\n- Abnormal thoracic spine morphology\n- Abnormal lumbar spine morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Short neck\n- Thick eyebrow\n- Carious teeth\n- Taurodontia\n- Pectus carinatum\n- Abnormality of the skeletal system\n- Dysostosis multiplex\n- Spasticity\n- Global developmental delay\n- Hyperreflexia\n- Hip dysplasia\n- Hepatosplenomegaly\n- Umbilical hernia\n- Secundum atrial septal defect\n- Cardiac arrest\n- Talipes equinovarus\n- Hydrops fetalis\n- Ventriculomegaly\n- Clonus\n- Spinal cord compression\n- Recurrent respiratory infections\n- Hepatomegaly\n- Kyphosis\n- Obstructive sleep apnea\n- Elbow flexion contracture\n- Distal amyotrophy\n- Decreased body weight\n- Cervical platyspondyly\n- Basilar impression\n- Enamel hypoplasia\n- Loss of ability to walk in first decade\n- Focal white matter lesions\n- Mandibular condyle hypoplasia\n- Anterior open-bite malocclusion\n- Abnormality of permanent molar morphology\n- Abnormal aortic valve cusp morphology\n- Abnormal thoracic spine morphology\n- Abnormal lumbar spine morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Cataract\n- Retinal degeneration\n- Abnormal vitreous humor morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/07836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Bladder diverticulum\n- Narrow face\n- Long face\n- Recurrent otitis media\n- Sensorineural hearing impairment\n- Astigmatism\n- Myopia\n- Depression\n- Anxiety\n- Pectus carinatum\n- Soft skin\n- Hemiparesis\n- Motor delay\n- Neonatal hypotonia\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Abnormal lung morphology\n- Scoliosis\n- Kyphoscoliosis\n- Decreased muscle mass\n- Short stature\n- Bipolar affective disorder\n- Anisocoria\n- Bilateral coxa valga\n- Feeding difficulties\n- Fatigue\n- Arterial occlusion\n- Periventricular white matter hyperintensities\n- Pseudoaneurysm\n- Rest dyspnea\n- Hypoesthesia\n- Celiac artery dissection\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Visual impairment\n- Rod-cone dystrophy\n- Intellectual disability\n- Truncal obesity\n- Polydipsia\n- Polyphagia\n- Hyperglycemia\n- Abnormal renal morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/07850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ocular albinism\n- Prolonged bleeding time\n- Impaired platelet aggregation\n- Spontaneous hematomas\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/07851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micrognathia\n- Protruding ear\n- Ptosis\n- Thick eyebrow\n- Autistic behavior\n- Reduced eye contact\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Ventriculomegaly\n- Long nose\n- Decreased muscle mass\n- Mild short stature\n- Relative macrocephaly\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/07852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pierre-Robin sequence\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/07853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Polycystic kidney dysplasia\n- Biliary tract abnormality\n- Polydactyly\n- Abnormal biliary tract morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/07854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Cleft soft palate\n- Retrognathia\n- Ankyloglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/07855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Nystagmus\n- Hypopigmentation of the skin\n- Ocular albinism\n- Iris hypopigmentation\n- White hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/07856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n- Abnormal heart morphology\n- Ventricular septal defect\n- Infantile muscular hypotonia\n- Sleep apnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/07857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Jaundice\n- Cardiomyopathy\n- Hypertrophic cardiomyopathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Global developmental delay\n- Generalized non-motor (absence) seizure\n- Generalized-onset seizure\n- Developmental regression\n- Somatic sensory dysfunction\n- Infantile muscular hypotonia\n- Intellectual disability, severe\n- Neurodevelopmental abnormality\n- Cerebral palsy\n- Low levels of vitamin D\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/07859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Myopia\n- Pectus excavatum\n- Hypotonia\n- Joint hypermobility\n- Scoliosis\n- Keloids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/07860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/07861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Thick lower lip vermilion\n- Low-set ears\n- Anteverted nares\n- Failure to thrive\n- Poor suck\n- Poor coordination\n- Limb hypertonia\n- Depressed nasal bridge\n- Congenital foot contractures\n- Apneic episodes in infancy\n- Axial hypotonia\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/07862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Proptosis\n- Cafe-au-lait spot\n- Hemangioma\n- Infantile sensorineural hearing impairment\n- Plexiform neurofibroma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/07863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Strabismus\n- Visual impairment\n- Thick eyebrow\n- Agitation\n- Autism\n- Compulsive behaviors\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Slender finger\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Slender build\n- Weight loss\n- Constipation\n- Loss of speech\n- Developmental regression\n- Scoliosis\n- Abnormality of temperature regulation\n- Prominent nasal tip\n- Attention deficit hyperactivity disorder\n- Cervical instability\n- Tented upper lip vermilion\n- Upturned corners of mouth\n- Tented philtrum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Agitation\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Hypotonia\n- Motor delay\n- Gait disturbance\n- Slurred speech\n- 1-3 toe syndactyly\n- Frontal bossing\n- Gait imbalance\n- Poor motor coordination\n- Intellectual disability, moderate\n- Sleep disturbance\n- Allergic rhinitis\n- Lactose intolerance\n- Prominent nasal tip\n- Speech apraxia\n- Typical absence seizure\n- Prominent forehead\n- Moderate global developmental delay\n- Impulsivity\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Broad nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Wide nasal bridge\n- Fair hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Wide nasal bridge\n- Fair hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Wide nasal bridge\n- Fair hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/07887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Nystagmus\n- Hypothyroidism\n- Lethargy\n- Global developmental delay\n- Neonatal hypotonia\n- Abnormal hip joint morphology\n- Laryngomalacia\n- Bradycardia\n- Neonatal hypoglycemia\n- Vomiting\n- Central apnea\n- Neonatal hyperbilirubinemia\n- Ganglioneuroblastoma\n- Feeding difficulties in infancy\n- Low levels of vitamin K\n- T-cell lymphoma\n- Grade I preterm intraventricular hemorrhage\n- Subdural hemorrhage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/07888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Nystagmus\n- Hypothyroidism\n- Lethargy\n- Global developmental delay\n- Neonatal hypotonia\n- Abnormal hip joint morphology\n- Laryngomalacia\n- Bradycardia\n- Neonatal hypoglycemia\n- Vomiting\n- Central apnea\n- Neonatal hyperbilirubinemia\n- Ganglioneuroblastoma\n- Feeding difficulties in infancy\n- Low levels of vitamin K\n- T-cell lymphoma\n- Grade I preterm intraventricular hemorrhage\n- Subdural hemorrhage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/07889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Sloping forehead\n- Narrow forehead\n- Micrognathia\n- Prominent nasal bridge\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Atypical behavior\n- Hyperorality\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Motor delay\n- Pes planus\n- Broad foot\n- Short foot\n- Hallux valgus\n- Broad-based gait\n- Highly arched eyebrow\n- Scoliosis\n- High, narrow palate\n- Kyphoscoliosis\n- Radioulnar synostosis\n- Short stature\n- Short fourth metatarsal\n- Limited elbow extension and supination\n- Decreased palmar creases\n- Low hanging columella\n- Short 5th metacarpal\n- Feeding difficulties\n- Abdominal obesity\n- Fatigable weakness of chewing muscles\n- Palilalia\n- Tics\n- Short proximal phalanx of the 3rd toe\n- Camptodactyly of finger\n- Atelectasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/07890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Sloping forehead\n- Narrow forehead\n- Micrognathia\n- Prominent nasal bridge\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Atypical behavior\n- Hyperorality\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Motor delay\n- Pes planus\n- Broad foot\n- Short foot\n- Hallux valgus\n- Broad-based gait\n- Highly arched eyebrow\n- Scoliosis\n- High, narrow palate\n- Kyphoscoliosis\n- Radioulnar synostosis\n- Short stature\n- Short fourth metatarsal\n- Limited elbow extension and supination\n- Decreased palmar creases\n- Low hanging columella\n- Short 5th metacarpal\n- Feeding difficulties\n- Abdominal obesity\n- Fatigable weakness of chewing muscles\n- Palilalia\n- Tics\n- Short proximal phalanx of the 3rd toe\n- Camptodactyly of finger\n- Atelectasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/07891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Sloping forehead\n- Narrow forehead\n- Micrognathia\n- Prominent nasal bridge\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Atypical behavior\n- Hyperorality\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Motor delay\n- Pes planus\n- Broad foot\n- Short foot\n- Hallux valgus\n- Broad-based gait\n- Highly arched eyebrow\n- Scoliosis\n- High, narrow palate\n- Kyphoscoliosis\n- Radioulnar synostosis\n- Short stature\n- Short fourth metatarsal\n- Limited elbow extension and supination\n- Decreased palmar creases\n- Low hanging columella\n- Short 5th metacarpal\n- Feeding difficulties\n- Abdominal obesity\n- Fatigable weakness of chewing muscles\n- Palilalia\n- Tics\n- Short proximal phalanx of the 3rd toe\n- Camptodactyly of finger\n- Atelectasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/07892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Atypical behavior\n- Compulsive behaviors\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Truncal obesity\n- Postural instability\n- Delayed gross motor development\n- Frontal upsweep of hair\n- Clumsiness\n- Language impairment\n- Expressive language delay\n- Apneic episodes precipitated by illness, fatigue, stress\n- Preauricular pit\n- 2-3 toe syndactyly\n- Sparse lateral eyebrow\n- Apneic episodes in infancy\n- Attention deficit hyperactivity disorder\n- Hallux varus\n- Microtia\n- Short 5th finger\n- Dermal translucency\n- Abnormal hair whorl\n- Receptive language delay\n- Prominent forehead\n- Broad eyebrow\n- Frequent temper tantrums\n- Weakness of facial musculature\n- Arachnoid cyst\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/07898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Hepatosplenomegaly\n- Recurrent fever\n- Lymphadenopathy\n- Elevated hepatic transaminase\n- Decreased circulating antibody level\n- Abnormal gallbladder morphology\n- Decreased proportion of immature B cells\n- Granuloma\n- Portal inflammation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/07899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Open mouth\n- Narrow forehead\n- Nystagmus\n- Oculomotor apraxia\n- Hypotonia\n- Global developmental delay\n- Growth delay\n- Frontal bossing\n- Dilated fourth ventricle\n- Thickened superior cerebellar peduncle\n- Poor head control\n- Highly arched eyebrow\n- Episodic tachypnea\n- Excessive salivation\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Aplasia\/Hypoplasia of the cerebellar vermis\n- Protruding tongue\n- Elongated superior cerebellar peduncle\n- Enlarged fossa interpeduncularis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/07900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/07910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Childhood-onset truncal obesity\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/07911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cleft palate\n- Hypertelorism\n- Upslanted palpebral fissure\n- Hyperpigmentation of the skin\n- Omphalocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Motor delay\n- Severe short stature\n- Relative macrocephaly\n- Bilateral sensorineural hearing impairment\n- Infantile muscular hypotonia\n- Feeding difficulties\n- Medullary nephrocalcinosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/07913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hemihypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/07914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n- Pectus excavatum\n- 1-3 toe syndactyly\n- Absent fingernail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/07915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Sensorineural hearing impairment\n- Wide nose\n- Short neck\n- Downslanted palpebral fissures\n- Rod-cone dystrophy\n- Long eyelashes\n- Hypermetropia\n- Thick eyebrow\n- Synophrys\n- Hirsutism\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Short foot\n- Facial hypertrichosis\n- Exaggerated cupid's bow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Sacral hypertrichosis\n- Elbow hypertrichosis\n- Curly eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Abnormal pinna morphology\n- Downslanted palpebral fissures\n- Long eyelashes\n- Exotropia\n- Synophrys\n- Widely spaced teeth\n- Hirsutism\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Patent ductus arteriosus\n- Low posterior hairline\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short stature\n- Depressed nasal bridge\n- Curly eyelashes\n- Narrow palpebral fissure\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Narrow mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Long philtrum\n- Widow's peak\n- Prominent nose\n- Long eyelashes\n- Synophrys\n- Narrow chest\n- Single transverse palmar crease\n- Hirsutism\n- Intellectual disability\n- Global developmental delay\n- Highly arched eyebrow\n- Short stature\n- Curly eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Microcephaly\n- Wide anterior fontanel\n- Micrognathia\n- Convex nasal ridge\n- Narrow nasal bridge\n- Abnormal retinal morphology\n- Cataract\n- Proptosis\n- Blue sclerae\n- Delayed speech and language development\n- Abnormal sternum morphology\n- Platyspondyly\n- Prominent superficial veins\n- Brachydactyly\n- Motor delay\n- Delayed closure of the anterior fontanelle\n- Talipes equinovarus\n- Short toe\n- Short distal phalanx of toe\n- Neutropenia\n- Spinal cord compression\n- Coxa valga\n- Platybasia\n- Osteoarthritis\n- Flared metaphysis\n- Madelung-like forearm deformities\n- Irregular vertebral endplates\n- Severe short stature\n- Decreased body weight\n- Progeroid facial appearance\n- Overtubulated long bones\n- Hypoplasia of proximal fibula\n- Hypoplastic vertebral bodies\n- Bilateral sensorineural hearing impairment\n- Pseudoepiphyses of the metacarpals\n- Low hanging columella\n- Short phalanx of finger\n- Short distal phalanx of finger\n- Short metacarpal\n- Ivory epiphyses of the phalanges of the hand\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent forehead\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/07919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureteropelvic junction obstruction\n- Hydronephrosis\n- Abnormality of the dentition\n- Hydrocephalus\n- Triangular face\n- Conductive hearing impairment\n- Cataract\n- Myopia\n- Dental crowding\n- Cupped ribs\n- Jaundice\n- Prominent scalp veins\n- Brachydactyly\n- Limited elbow extension\n- Growth delay\n- Talipes equinovarus\n- Pes planus\n- Neutropenia\n- Frontal bossing\n- Constipation\n- Recurrent aspiration pneumonia\n- Recurrent respiratory infections\n- Proportionate short stature\n- Decreased body weight\n- Premature eruption of permanent teeth\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Anisometropia\n- Recurrent streptococcal infections\n- Exophoria\n- Sparse eyebrow\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/07920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureteropelvic junction obstruction\n- Hydronephrosis\n- Abnormality of the dentition\n- Hydrocephalus\n- Triangular face\n- Conductive hearing impairment\n- Cataract\n- Myopia\n- Dental crowding\n- Cupped ribs\n- Jaundice\n- Prominent scalp veins\n- Brachydactyly\n- Limited elbow extension\n- Growth delay\n- Talipes equinovarus\n- Pes planus\n- Neutropenia\n- Frontal bossing\n- Constipation\n- Recurrent aspiration pneumonia\n- Recurrent respiratory infections\n- Proportionate short stature\n- Decreased body weight\n- Premature eruption of permanent teeth\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Anisometropia\n- Recurrent streptococcal infections\n- Exophoria\n- Sparse eyebrow\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/07921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Low anterior hairline\n- Nevus flammeus\n- Intrauterine growth retardation\n- Frontal upsweep of hair\n- obsolete Laterally deviated terminal thumb phalanx\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/07922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Macrotia\n- Recurrent otitis media\n- Hypermetropia\n- Small for gestational age\n- Poor suck\n- Hypoplasia of the corpus callosum\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Mild global developmental delay\n- Feeding difficulties\n- Stereotypical hand wringing\n- Setting-sun eye phenomenon\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/07923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Postaxial hand polydactyly\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/07924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/07925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/07927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/07928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/07933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/07934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Median cleft lip\n- Hand polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/07935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Thin upper lip vermilion\n- Malar flattening\n- Short philtrum\n- Broad forehead\n- Prominent nasal bridge\n- Webbed neck\n- Thickened nuchal skin fold\n- Deeply set eye\n- Periorbital fullness\n- Anxiety\n- Sprengel anomaly\n- Single transverse palmar crease\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Pes planus\n- Short foot\n- Overlapping toe\n- Preauricular pit\n- Intellectual disability, borderline\n- Bilateral cryptorchidism\n- Feeding difficulties in infancy\n- Underdeveloped crus of the helix\n- Thin lower lip vermilion\n- Impaired tactile sensation\n- Chronic constipation\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- High palate\n- Macrocephaly\n- Epicanthus\n- Astigmatism\n- Deeply set eye\n- Thick eyebrow\n- Periorbital fullness\n- Synophrys\n- Widely spaced teeth\n- Single transverse palmar crease\n- Hypotonia\n- Motor delay\n- Joint laxity\n- Large for gestational age\n- Atrial septal defect\n- Dysphagia\n- Poor suck\n- Downturned corners of mouth\n- Large earlobe\n- Overweight\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft soft palate\n- Microcephaly\n- Deeply set eye\n- Periorbital fullness\n- Dental malocclusion\n- Depression\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Acne\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Chiari malformation\n- Abnormal cerebellar vermis morphology\n- Obstructive sleep apnea\n- Delayed fine motor development\n- Feeding difficulties\n- Otitis media with effusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Velopharyngeal insufficiency\n- Macrocephaly\n- Deeply set eye\n- Periorbital fullness\n- obsolete Mood swings\n- Autistic behavior\n- Short attention span\n- Anxiety\n- Delayed speech and language development\n- Poor speech\n- Obstructive sleep apnea\n- Overweight\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Dental malocclusion\n- Anxiety\n- Absent speech\n- Asthma\n- Intellectual disability, borderline\n- Midface retrusion\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Hypermetropia\n- Amblyopia\n- Delayed speech and language development\n- Abnormal nonverbal communicative behavior\n- Jaundice\n- Toe clinodactyly\n- Sleep disturbance\n- Deficit in grammar\n- Almond-shaped palpebral fissure\n- Prominent forehead\n- Auditory sensitivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Synophrys\n- Single transverse palmar crease\n- Hypertrichosis\n- Global developmental delay\n- Joint laxity\n- Ventricular septal defect\n- Pes planus\n- Broad-based gait\n- Unsteady gait\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short uvula\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Synophrys\n- Single transverse palmar crease\n- Hypertrichosis\n- Global developmental delay\n- Joint laxity\n- Ventricular septal defect\n- Pes planus\n- Broad-based gait\n- Unsteady gait\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short uvula\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Synophrys\n- Single transverse palmar crease\n- Hypertrichosis\n- Global developmental delay\n- Joint laxity\n- Ventricular septal defect\n- Pes planus\n- Broad-based gait\n- Unsteady gait\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short uvula\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Enlarged kidney\n- Narrow mouth\n- High palate\n- Macrocephaly\n- Low-set, posteriorly rotated ears\n- Overfolded helix\n- Depressed nasal tip\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Hypermetropia\n- Esotropia\n- Long palpebral fissure\n- Pectus excavatum\n- Melanocytic nevus\n- Large hands\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Umbilical hernia\n- Overgrowth\n- Intellectual disability, moderate\n- Downturned corners of mouth\n- 2-3 toe syndactyly\n- Thoracic hypoplasia\n- Curly eyelashes\n- Short finger\n- Prominent crus of helix\n- Prominent eyelashes\n- Broad thumb\n- Splayed toes\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Enlarged kidney\n- Narrow mouth\n- High palate\n- Macrocephaly\n- Low-set, posteriorly rotated ears\n- Overfolded helix\n- Depressed nasal tip\n- Anteverted nares\n- Downslanted palpebral fissures\n- Long eyelashes\n- Hypermetropia\n- Esotropia\n- Long palpebral fissure\n- Pectus excavatum\n- Melanocytic nevus\n- Large hands\n- Hypotonia\n- Global developmental delay\n- Agenesis of corpus callosum\n- Umbilical hernia\n- Overgrowth\n- Intellectual disability, moderate\n- Downturned corners of mouth\n- 2-3 toe syndactyly\n- Thoracic hypoplasia\n- Curly eyelashes\n- Short finger\n- Prominent crus of helix\n- Prominent eyelashes\n- Broad thumb\n- Splayed toes\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Epicanthus\n- Overfolded helix\n- Bulbous nose\n- Hyperpigmentation of the skin\n- Nevus flammeus\n- Global developmental delay\n- Generalized hypotonia\n- Cerebellar hypoplasia\n- Constipation\n- Rigidity\n- Enlarged cisterna magna\n- Poor speech\n- Prominent metopic ridge\n- Increased laxity of fingers\n- Multiple cafe-au-lait spots\n- Everted upper lip vermilion\n- Moderate conductive hearing impairment\n- Distributed along Blaschko lines\n- Lower limb asymmetry\n- Upper limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Long palpebral fissure\n- Carious teeth\n- Abnormal posterior cranial fossa morphology\n- Tapered finger\n- Prominent fingertip pads\n- Seizure\n- Generalized hypotonia\n- Joint hypermobility\n- Broad foot\n- Short foot\n- Deep philtrum\n- Gastroesophageal reflux\n- Curved linear dimple below the lower lip\n- Abnormal cerebellar vermis morphology\n- Sleep disturbance\n- Hip dislocation\n- Bilateral single transverse palmar creases\n- Severe global developmental delay\n- Enlarged cerebellum\n- Chronic constipation\n- Enlarged brainstem\n- Esophoria\n- Overweight\n- Low levels of vitamin D\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- High palate\n- Macrocephaly\n- Prominent occiput\n- Epicanthus\n- Overfolded helix\n- Wide nasal bridge\n- Deeply set eye\n- Downslanted palpebral fissures\n- Periorbital fullness\n- Delayed speech and language development\n- Abnormality of the thymus\n- Hypotonia\n- Motor delay\n- Constipation\n- Gastroesophageal reflux\n- Polymicrogyria\n- Delayed CNS myelination\n- Recurrent infections\n- Prominent metopic ridge\n- Recurrent pneumonia\n- Laryngeal cleft\n- Palmar hyperkeratosis\n- Overweight\n- Scaphocephaly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypotonia\n- Global developmental delay\n- Frontal bossing\n- Broad-based gait\n- Delayed gross motor development\n- Expressive language delay\n- Tented philtrum\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Long philtrum\n- Deeply set eye\n- Hypermetropia\n- Compulsive behaviors\n- Delayed speech and language development\n- Delayed puberty\n- Abnormal posterior cranial fossa morphology\n- Global developmental delay\n- Meningitis\n- Achilles tendon contracture\n- Migraine\n- Intermittent diarrhea\n- Incoordination\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Genu valgum\n- Short stature\n- 2-3 toe syndactyly\n- Decreased testicular size\n- Incisor macrodontia\n- Broad eyebrow\n- Generalized abnormality of skin\n- Hair-pulling\n- Thick vermilion border\n- Enlarged brainstem\n- Narrow palpebral fissure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Seizure\n- Ataxia\n- Hypotonia\n- Involuntary movements\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Epicanthus\n- High forehead\n- Posteriorly rotated ears\n- Protruding ear\n- Periorbital fullness\n- Long palpebral fissure\n- Delayed speech and language development\n- Pectus excavatum\n- Lymphedema\n- Laryngomalacia\n- Bicuspid aortic valve\n- Overlapping toe\n- Dysphagia\n- Gastroesophageal reflux\n- Bilateral cryptorchidism\n- High anterior hairline\n- Ankyloglossia\n- Bloody diarrhea\n- Overweight\n- Abnormality of the maxillary sinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Narrow palate\n- Facial hypotonia\n- Recurrent otitis media\n- Hypotonia\n- Motor delay\n- Joint laxity\n- Constipation\n- Enlarged cisterna magna\n- Poor speech\n- Delayed fine motor development\n- Moderate global developmental delay\n- Bronchitis\n- Dilation of Virchow-Robin spaces\n- Enlarged brainstem\n- Abnormal preputium morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Downslanted palpebral fissures\n- Hypotonia\n- Frontal bossing\n- Constipation\n- Microtia\n- Infantile muscular hypotonia\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Downslanted palpebral fissures\n- Hypotonia\n- Frontal bossing\n- Constipation\n- Microtia\n- Infantile muscular hypotonia\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Bifid uvula\n- High palate\n- Macrocephaly\n- Dolichocephaly\n- Smooth philtrum\n- Short chin\n- High forehead\n- Protruding ear\n- Dental malocclusion\n- Delayed speech and language development\n- Hypotonia\n- Neonatal hypotonia\n- Joint laxity\n- Hypernasal speech\n- Atrial septal defect\n- Patent foramen ovale\n- Pes planus\n- Constipation\n- Drooling\n- Neonatal respiratory distress\n- Deviated nasal septum\n- Hyperechogenic kidneys\n- Reduced renal corticomedullary differentiation\n- Uplifted earlobe\n- Moderate global developmental delay\n- Stuttering\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Bifid uvula\n- High palate\n- Macrocephaly\n- Dolichocephaly\n- Smooth philtrum\n- Short chin\n- High forehead\n- Protruding ear\n- Dental malocclusion\n- Delayed speech and language development\n- Hypotonia\n- Neonatal hypotonia\n- Joint laxity\n- Hypernasal speech\n- Atrial septal defect\n- Patent foramen ovale\n- Pes planus\n- Constipation\n- Drooling\n- Neonatal respiratory distress\n- Deviated nasal septum\n- Hyperechogenic kidneys\n- Reduced renal corticomedullary differentiation\n- Uplifted earlobe\n- Moderate global developmental delay\n- Stuttering\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/07958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/07959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/07961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/07962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/07963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/07964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/07965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/07966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Microcephaly\n- Hypertelorism\n- Narrow forehead\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Visual impairment\n- Global developmental delay\n- Dandy-Walker malformation\n- Brisk reflexes\n- Ventricular septal defect\n- Clonus\n- Limb hypertonia\n- Muscle spasm\n- CNS hypomyelination\n- Mild short stature\n- 2-3 toe syndactyly\n- Prominent metopic ridge\n- Axial hypotonia\n- Attached earlobe\n- Brain atrophy\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/07967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Otitis media\n- Delayed speech and language development\n- Hypertension\n- Ataxia\n- Motor delay\n- Specific learning disability\n- Lower limb spasticity\n- Dysdiadochokinesis\n- Intention tremor\n- Clumsiness\n- Intellectual disability, moderate\n- Action tremor\n- Hypercholesterolemia\n- Long nose\n- Depressed nasal bridge\n- Lower limb hypertonia\n- Hyperactive patellar reflex\n- Low hanging columella\n- EEG with spike-wave complexes (<2.5 Hz)\n- Speech apraxia\n- Ankle clonus\n- Bronchitis\n- Diminished ability to concentrate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/07968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Otitis media\n- Delayed speech and language development\n- Hypertension\n- Global developmental delay\n- Lower limb spasticity\n- Gait ataxia\n- Dysdiadochokinesis\n- Intention tremor\n- Pneumonia\n- Postural instability\n- Clumsiness\n- Intellectual disability, moderate\n- Thoracic kyphosis\n- Long nose\n- Depressed nasal bridge\n- Type II diabetes mellitus\n- Lower limb hypertonia\n- Hyperactive patellar reflex\n- Benign prostatic hyperplasia\n- Low hanging columella\n- EEG with spike-wave complexes (<2.5 Hz)\n- Speech apraxia\n- Ankle clonus\n- Anomic aphasia\n- Alternating exotropia\n- Impaired toe-walking ability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/07969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Facial hypotonia\n- Recurrent otitis media\n- Exotropia\n- Delayed speech and language development\n- Brachydactyly\n- Ataxia\n- Hypotonia\n- Tremor\n- Hoarse voice\n- Ventricular septal defect\n- Atrial septal defect\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Transposition of the great arteries\n- Pes planus\n- Achilles tendon contracture\n- Sandal gap\n- Dysdiadochokinesis\n- Intention tremor\n- Postural instability\n- Clumsiness\n- Intellectual disability, moderate\n- Incomprehensible speech\n- Depressed nasal bridge\n- Lower limb hypertonia\n- Poor fine motor coordination\n- Hyperactive patellar reflex\n- Pes valgus\n- Speech apraxia\n- Ankle clonus\n- Hypertropia\n- Hypoplastic right atrium\n- Brachioradialis hyperreflexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/07970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/07971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/07972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Facial hypotonia\n- Recurrent otitis media\n- Wide nasal bridge\n- Broad nasal tip\n- Delayed speech and language development\n- Sacral dimple\n- Brachydactyly\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Hoarse voice\n- Pes planus\n- Achilles tendon contracture\n- Sandal gap\n- Constipation\n- Lower limb spasticity\n- Dysdiadochokinesis\n- Intention tremor\n- Postural instability\n- Clumsiness\n- Intellectual disability, moderate\n- Incomprehensible speech\n- High, narrow palate\n- Lumbar hyperlordosis\n- Short stature\n- Depressed nasal bridge\n- Lower limb hypertonia\n- Poor fine motor coordination\n- Hyperactive patellar reflex\n- Pes valgus\n- Aplasia\/Hypoplasia of the middle phalanx of the 5th finger\n- Low hanging columella\n- EEG with spike-wave complexes (<2.5 Hz)\n- Speech apraxia\n- EEG with continuous slow activity\n- Prominent forehead\n- Ankle clonus\n- Snoring\n- Exophoria\n- Hypertropia\n- Clinodactyly\n- Anomic aphasia\n- Enlarged tonsils\n- Alternating exotropia\n- Brachioradialis hyperreflexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/07973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Facial hypotonia\n- Recurrent otitis media\n- Wide nasal bridge\n- Broad nasal tip\n- Delayed speech and language development\n- Sacral dimple\n- Brachydactyly\n- Ataxia\n- Hypotonia\n- Global developmental delay\n- Failure to thrive\n- Hoarse voice\n- Pes planus\n- Achilles tendon contracture\n- Sandal gap\n- Constipation\n- Lower limb spasticity\n- Dysdiadochokinesis\n- Intention tremor\n- Postural instability\n- Clumsiness\n- Intellectual disability, moderate\n- Incomprehensible speech\n- High, narrow palate\n- Lumbar hyperlordosis\n- Short stature\n- Depressed nasal bridge\n- Lower limb hypertonia\n- Poor fine motor coordination\n- Hyperactive patellar reflex\n- Pes valgus\n- Aplasia\/Hypoplasia of the middle phalanx of the 5th finger\n- Low hanging columella\n- EEG with spike-wave complexes (<2.5 Hz)\n- Speech apraxia\n- EEG with continuous slow activity\n- Prominent forehead\n- Ankle clonus\n- Snoring\n- Exophoria\n- Hypertropia\n- Clinodactyly\n- Anomic aphasia\n- Enlarged tonsils\n- Alternating exotropia\n- Brachioradialis hyperreflexia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/07974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Open mouth\n- High palate\n- Everted lower lip vermilion\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Triangular nasal tip\n- Anteverted nares\n- Strabismus\n- Hypotonia\n- Global developmental delay\n- Atrial septal defect\n- Short nose\n- Depressed nasal bridge\n- Enamel hypoplasia\n- Cerebral dysmyelination\n- CNS demyelination\n- Elevated circulating follicle stimulating hormone level\n- Female external genitalia in individual with 46,XY karyotype\n- Tented upper lip vermilion\n- Protruding tongue\n- HbH hemoglobin\n- Hypoplastic female external genitalia\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Open mouth\n- High palate\n- Everted lower lip vermilion\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Triangular nasal tip\n- Anteverted nares\n- Strabismus\n- Hypotonia\n- Global developmental delay\n- Atrial septal defect\n- Short nose\n- Depressed nasal bridge\n- Enamel hypoplasia\n- Cerebral dysmyelination\n- CNS demyelination\n- Elevated circulating follicle stimulating hormone level\n- Female external genitalia in individual with 46,XY karyotype\n- Tented upper lip vermilion\n- Protruding tongue\n- HbH hemoglobin\n- Hypoplastic female external genitalia\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft soft palate\n- Triangular mouth\n- Microcephaly\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Telecanthus\n- Optic disc pallor\n- Abnormality of the skeletal system\n- Neonatal hypotonia\n- Absent speech\n- Abnormal foot morphology\n- Overlapping toe\n- Vomiting\n- Sudden episodic apnea\n- Short nose\n- Severe short stature\n- Excessive salivation\n- Depressed nasal bridge\n- Abnormality of the male genitalia\n- Overlapping fingers\n- Intellectual disability, severe\n- Midface retrusion\n- HbH hemoglobin\n- Feeding difficulties\n- Cyanotic episode\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Triangular mouth\n- Microcephaly\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Abnormality of the skeletal system\n- Cyanosis\n- Seizure\n- Hypotonia\n- Lethargy\n- Abnormal foot morphology\n- Constipation\n- Poor suck\n- Kyphoscoliosis\n- Sudden episodic apnea\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Positional foot deformity\n- Wide intermamillary distance\n- Abnormality of the male genitalia\n- Abnormal position of hair whorl\n- Intellectual disability, severe\n- HbH hemoglobin\n- Abnormal renal morphology\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Cryptorchidism\n- Micropenis\n- Abnormality of the dentition\n- Triangular mouth\n- High palate\n- Epicanthus\n- Low-set ears\n- Triangular nasal tip\n- Anteverted nares\n- Myopia\n- Emotional lability\n- Pectus carinatum\n- Nephrolithiasis\n- Tapered finger\n- Seizure\n- Lethargy\n- Absent speech\n- Umbilical hernia\n- Atrial septal defect\n- Abnormal foot morphology\n- Overlapping toe\n- Talipes calcaneovalgus\n- Vomiting\n- Constipation\n- Hiatus hernia\n- Coxa valga\n- Kyphoscoliosis\n- Recurrent lower respiratory tract infections\n- Sudden episodic apnea\n- Short nose\n- Excessive salivation\n- Depressed nasal bridge\n- Temperature instability\n- Overlapping fingers\n- Midface retrusion\n- HbH hemoglobin\n- Feeding difficulties\n- Abnormal renal morphology\n- Flexion contracture of finger\n- obsolete Psychomotor retardation\n- Clinodactyly\n- Cardiac conduction abnormality\n- Abnormal ear morphology\n- Abnormal preputium morphology\n- Submucous cleft of soft and hard palate\n- Peripheral cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Cryptorchidism\n- Hypospadias\n- Triangular mouth\n- Hearing impairment\n- Keratitis\n- Visual impairment\n- Telecanthus\n- Conjunctivitis\n- Carious teeth\n- Pectus carinatum\n- Short sternum\n- Tapered finger\n- Seizure\n- Abnormal foot morphology\n- Bilateral talipes equinovarus\n- Overlapping toe\n- Vomiting\n- Constipation\n- Cerebral atrophy\n- Psychomotor deterioration\n- Coxa valga\n- Kyphoscoliosis\n- Recurrent lower respiratory tract infections\n- Abnormal vertebral morphology\n- Excessive salivation\n- Drumstick terminal phalanges\n- Widely-spaced incisors\n- Overlapping fingers\n- Midface retrusion\n- HbH hemoglobin\n- Feeding difficulties\n- obsolete Psychomotor retardation\n- Clinodactyly\n- obsolete Small scrotum\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Triangular mouth\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Telecanthus\n- Emotional lability\n- Abnormality of the skeletal system\n- Cyanosis\n- Neonatal hypotonia\n- Flexion contracture\n- Patent ductus arteriosus\n- Secundum atrial septal defect\n- Sleep disturbance\n- Recurrent lower respiratory tract infections\n- Short nose\n- Excessive salivation\n- Short stature\n- Depressed nasal bridge\n- Apneic episodes in infancy\n- Joint contracture of the 5th finger\n- Abnormality of the male genitalia\n- Intellectual disability, severe\n- Midface retrusion\n- HbH hemoglobin\n- Self-biting\n- obsolete Psychomotor retardation\n- Cardiac conduction abnormality\n- Abnormal ear morphology\n- Neonatal seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Triangular mouth\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Carious teeth\n- Emotional lability\n- Abnormality of the skeletal system\n- Global developmental delay\n- Vomiting\n- Gastroesophageal reflux\n- Pneumonia\n- Anarthria\n- Delayed skeletal maturation\n- Recurrent lower respiratory tract infections\n- Short nose\n- Excessive salivation\n- Widely-spaced incisors\n- Intellectual disability, severe\n- Midface retrusion\n- HbH hemoglobin\n- Inappropriate crying\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Triangular mouth\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Carious teeth\n- Emotional lability\n- Abnormality of the skeletal system\n- Global developmental delay\n- Vomiting\n- Gastroesophageal reflux\n- Pneumonia\n- Anarthria\n- Delayed skeletal maturation\n- Recurrent lower respiratory tract infections\n- Short nose\n- Excessive salivation\n- Widely-spaced incisors\n- Intellectual disability, severe\n- Midface retrusion\n- HbH hemoglobin\n- Inappropriate crying\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular mouth\n- Coarse facial features\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Emotional lability\n- Agitation\n- Abnormality of the skeletal system\n- Sacral dimple\n- Neonatal hypotonia\n- Absent speech\n- Abnormal foot morphology\n- Overlapping toe\n- Spina bifida\n- Delayed skeletal maturation\n- Short nose\n- Abnormal vertebral morphology\n- Excessive salivation\n- Short stature\n- Depressed nasal bridge\n- Short lower limbs\n- Overlapping fingers\n- Intellectual disability, severe\n- Midface retrusion\n- HbH hemoglobin\n- Head-banging\n- Self-biting\n- Abnormal ear morphology\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular mouth\n- Coarse facial features\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Emotional lability\n- Agitation\n- Abnormality of the skeletal system\n- Sacral dimple\n- Neonatal hypotonia\n- Absent speech\n- Abnormal foot morphology\n- Overlapping toe\n- Spina bifida\n- Delayed skeletal maturation\n- Short nose\n- Abnormal vertebral morphology\n- Excessive salivation\n- Short stature\n- Depressed nasal bridge\n- Short lower limbs\n- Overlapping fingers\n- Intellectual disability, severe\n- Midface retrusion\n- HbH hemoglobin\n- Head-banging\n- Self-biting\n- Abnormal ear morphology\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/07985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Downslanted palpebral fissures\n- Seizure\n- Growth delay\n- Pulmonic stenosis\n- Tachycardia\n- Curly hair\n- Abnormal calvaria morphology\n- Neuroblastoma\n- Hypoplastic nasal bridge\n- Sparse hair\n- Underdeveloped supraorbital ridges\n- Intellectual disability, severe\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Bird-like facies\n- obsolete Mood swings\n- Delayed speech and language development\n- Hyperpigmentation of the skin\n- Seizure\n- Hemiplegia\n- Sleep disturbance\n- Aphasia\n- Poor appetite\n- Sparse hair\n- Lower limb pain\n- Stuttering\n- Absent pulse\n- Cutaneous wound\n- Arterial stenosis\n- Hypercoagulability\n- Skin ulcer\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/07989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Microcephaly\n- Facial asymmetry\n- Abnormal pinna morphology\n- Convex nasal ridge\n- Nephrolithiasis\n- Failure to thrive\n- Premature birth\n- Pes planus\n- Decreased circulating IgA level\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Decreased body weight\n- Morgagni diaphragmatic hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/07990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Retrognathia\n- Small earlobe\n- Macrotia\n- Protruding ear\n- Convex nasal ridge\n- Prominent nose\n- Agenesis of corpus callosum\n- Pachygyria\n- Cerebellar vermis hypoplasia\n- Abnormal cerebral cortex morphology\n- Clinodactyly of the 5th finger\n- Short stature\n- Knee flexion contracture\n- Bilateral single transverse palmar creases\n- Feeding difficulties\n- Central nervous system cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/07991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypospadias\n- Microcephaly\n- Sloping forehead\n- Protruding ear\n- Proptosis\n- Single transverse palmar crease\n- Global developmental delay\n- Absent speech\n- Failure to thrive\n- Growth delay\n- Small for gestational age\n- Talipes equinovarus\n- obsolete Large beaked nose\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/07992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Strabismus\n- Ptosis\n- Nystagmus\n- Global developmental delay\n- Sparse scalp hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/07993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/07994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/07995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/07996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/07997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/07998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/07999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Mandibular prognathia\n- Hypertelorism\n- Low-set ears\n- Triangular nasal tip\n- Anteverted nares\n- Upslanted palpebral fissure\n- Diastema\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Generalized hypotonia\n- Weak cry\n- Poor suck\n- Bilateral tonic-clonic seizure\n- Scoliosis\n- Kyphosis\n- Short nose\n- Depressed nasal bridge\n- Widely-spaced incisors\n- U-Shaped upper lip vermilion\n- Midface retrusion\n- HbH hemoglobin\n- Flat face\n- Thick vermilion border\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Mandibular prognathia\n- Hypertelorism\n- Low-set ears\n- Triangular nasal tip\n- Anteverted nares\n- Upslanted palpebral fissure\n- Diastema\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Generalized hypotonia\n- Weak cry\n- Poor suck\n- Bilateral tonic-clonic seizure\n- Scoliosis\n- Kyphosis\n- Short nose\n- Depressed nasal bridge\n- Widely-spaced incisors\n- U-Shaped upper lip vermilion\n- Midface retrusion\n- HbH hemoglobin\n- Flat face\n- Thick vermilion border\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Epicanthus\n- Single umbilical artery\n- Absent speech\n- Brisk reflexes\n- Hepatosplenomegaly\n- Intrauterine growth retardation\n- Frontal upsweep of hair\n- Preauricular pit\n- Depressed nasal bridge\n- Bilateral camptodactyly\n- Severe muscular hypotonia\n- Severe global developmental delay\n- HbH hemoglobin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micropenis\n- Everted lower lip vermilion\n- Hypertelorism\n- Widow's peak\n- Low-set ears\n- Absent speech\n- Ventriculomegaly\n- Frontal upsweep of hair\n- Abnormal cerebral white matter morphology\n- Short nose\n- Hypochromic microcytic anemia\n- Depressed nasal bridge\n- Severe muscular hypotonia\n- Multiple cafe-au-lait spots\n- Tented upper lip vermilion\n- Anisocytosis\n- Severe global developmental delay\n- HbH hemoglobin\n- Decreased mean corpuscular volume\n- Dacryocytosis\n- Persistent head lag\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Testicular atrophy\n- Hydrocele testis\n- Triangular mouth\n- Epicanthus\n- Hypertelorism\n- Telecanthus\n- Delayed puberty\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Ventricular septal defect\n- Short distal phalanx of toe\n- Hypochromic anemia\n- Microcytic anemia\n- Cerebral atrophy\n- Delayed skeletal maturation\n- Kyphosis\n- Bruxism\n- Clinodactyly of the 5th finger\n- Short stature\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Decreased testicular size\n- Short distal phalanx of finger\n- Bilateral coxa valga\n- HbH hemoglobin\n- Unilateral cryptorchidism\n- Impaired continence\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Testicular atrophy\n- Hydrocele testis\n- Triangular mouth\n- Epicanthus\n- Hypertelorism\n- Telecanthus\n- Delayed puberty\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Ventricular septal defect\n- Short distal phalanx of toe\n- Hypochromic anemia\n- Microcytic anemia\n- Cerebral atrophy\n- Delayed skeletal maturation\n- Kyphosis\n- Bruxism\n- Clinodactyly of the 5th finger\n- Short stature\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Decreased testicular size\n- Short distal phalanx of finger\n- Bilateral coxa valga\n- HbH hemoglobin\n- Unilateral cryptorchidism\n- Impaired continence\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Abnormal testis morphology\n- Epicanthus\n- Strabismus\n- Telecanthus\n- Global developmental delay\n- Pneumonia\n- Delayed skeletal maturation\n- Ovoid vertebral bodies\n- Depressed nasal bridge\n- Drumstick terminal phalanges\n- Severe muscular hypotonia\n- Aplasia\/Hypoplasia involving the sinuses\n- Bilateral coxa valga\n- U-Shaped upper lip vermilion\n- Abnormal premolar morphology\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Urinary incontinence\n- Abnormal testis morphology\n- Wide mouth\n- Abnormality of the dentition\n- Microcephaly\n- Mandibular prognathia\n- Hypotonia\n- Global developmental delay\n- Hypertonia\n- Absent speech\n- Anemia\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Inability to walk\n- Bowel incontinence\n- Absent frontal sinuses\n- Delayed skeletal maturation\n- Kyphosis\n- Severe short stature\n- Thoracolumbar kyphosis\n- Wide tufts of distal phalanges\n- Decreased testicular size\n- Feeding difficulties in infancy\n- Supernumerary tooth\n- EEG with focal sharp waves\n- Midface retrusion\n- HbH hemoglobin\n- Tongue thrusting\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Urinary incontinence\n- Abnormal testis morphology\n- Wide mouth\n- Abnormality of the dentition\n- Microcephaly\n- Mandibular prognathia\n- Hypotonia\n- Global developmental delay\n- Hypertonia\n- Absent speech\n- Anemia\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Inability to walk\n- Bowel incontinence\n- Absent frontal sinuses\n- Delayed skeletal maturation\n- Kyphosis\n- Severe short stature\n- Thoracolumbar kyphosis\n- Wide tufts of distal phalanges\n- Decreased testicular size\n- Feeding difficulties in infancy\n- Supernumerary tooth\n- EEG with focal sharp waves\n- Midface retrusion\n- HbH hemoglobin\n- Tongue thrusting\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Urinary incontinence\n- Abnormal testis morphology\n- Wide mouth\n- Abnormality of the dentition\n- Microcephaly\n- Mandibular prognathia\n- Hypotonia\n- Global developmental delay\n- Hypertonia\n- Absent speech\n- Anemia\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Inability to walk\n- Bowel incontinence\n- Absent frontal sinuses\n- Delayed skeletal maturation\n- Kyphosis\n- Severe short stature\n- Thoracolumbar kyphosis\n- Wide tufts of distal phalanges\n- Decreased testicular size\n- Feeding difficulties in infancy\n- Supernumerary tooth\n- EEG with focal sharp waves\n- Midface retrusion\n- HbH hemoglobin\n- Tongue thrusting\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Facial asymmetry\n- Micrognathia\n- Low-set ears\n- Convex nasal ridge\n- Prominent nose\n- Delayed speech and language development\n- Global developmental delay\n- Growth delay\n- Curly hair\n- Red hair\n- Brittle hair\n- Intellectual disability, moderate\n- Severe short stature\n- Clinodactyly of the 5th finger\n- Vascular tortuosity\n- Esodeviation\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Bird-like facies\n- Global developmental delay\n- Severe short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Sloping forehead\n- Micrognathia\n- Convex nasal ridge\n- 11 pairs of ribs\n- Selective tooth agenesis\n- Intellectual disability, moderate\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Few cafe-au-lait spots\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Sloping forehead\n- Micrognathia\n- Convex nasal ridge\n- Upslanted palpebral fissure\n- Intellectual disability, mild\n- Congenital hip dislocation\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Short stature\n- Few cafe-au-lait spots\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Sloping forehead\n- Micrognathia\n- Convex nasal ridge\n- Strabismus\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Delayed skeletal maturation\n- Radial bowing\n- Severe short stature\n- Abnormality of the radial head\n- Clinodactyly of the 5th finger\n- Pseudoepiphyses of second metacarpal\n- Few cafe-au-lait spots\n- Midface retrusion\n- Impaired ability to shift attention\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Microcephaly\n- Narrow face\n- Retrognathia\n- Narrow forehead\n- Micrognathia\n- Low-set ears\n- Strabismus\n- Cataract\n- Microphthalmia\n- Delayed speech and language development\n- Motor delay\n- Intrauterine growth retardation\n- Small for gestational age\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Microcephaly\n- Narrow face\n- Retrognathia\n- Narrow forehead\n- Micrognathia\n- Low-set ears\n- Abnormally large globe\n- Intellectual disability, mild\n- Intrauterine growth retardation\n- Small for gestational age\n- Decreased body weight\n- Bilateral sensorineural hearing impairment\n- Severe postnatal growth retardation\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Bird-like facies\n- Prelingual sensorineural hearing impairment\n- Apathy\n- Intellectual disability\n- Atrioventricular block\n- Severe short stature\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Retrognathia\n- Facial asymmetry\n- Micrognathia\n- Widow's peak\n- Absent earlobe\n- Telecanthus\n- Dental crowding\n- Dental malocclusion\n- Abnormality of the hand\n- Intellectual disability\n- Congenital hip dislocation\n- Intrauterine growth retardation\n- Abnormal foot morphology\n- Pes planus\n- Hallux valgus\n- Short toe\n- Sandal gap\n- Recurrent upper respiratory tract infections\n- Dislocated radial head\n- Hip contracture\n- Proportionate short stature\n- Severe short stature\n- obsolete Large beaked nose\n- Knee flexion contracture\n- Microtia\n- Short finger\n- Tapered toe\n- Camptodactyly\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Facial asymmetry\n- Short chin\n- Sloping forehead\n- Micrognathia\n- Absent earlobe\n- Telecanthus\n- Proptosis\n- Dental crowding\n- Dental malocclusion\n- Atypical behavior\n- Abnormality of the hand\n- Brachydactyly\n- Intellectual disability\n- Intrauterine growth retardation\n- Small for gestational age\n- Abnormal foot morphology\n- Talipes equinovarus\n- Sandal gap\n- High, narrow palate\n- Abnormal respiratory system physiology\n- Recurrent bronchitis\n- Dislocated radial head\n- Hip contracture\n- obsolete Large beaked nose\n- Clinodactyly of the 5th finger\n- Knee dislocation\n- Clinodactyly of the 2nd toe\n- Knee flexion contracture\n- Microtia\n- Moderately short stature\n- Feeding difficulties in infancy\n- Pseudoepiphysis of the proximal phalanx of the 5th finger\n- Short finger\n- Pseudoepiphysis of the proximal phalanx of the 2nd finger\n- Carpal synostosis\n- Short palpebral fissure\n- Type I diabetes mellitus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Facial asymmetry\n- Micrognathia\n- Absent earlobe\n- Telecanthus\n- Proptosis\n- Dental crowding\n- Dental malocclusion\n- Abnormality of the hand\n- Brachydactyly\n- Intellectual disability\n- Intrauterine growth retardation\n- Small for gestational age\n- Abnormal foot morphology\n- Sandal gap\n- Elbow flexion contracture\n- Dislocated radial head\n- Hip contracture\n- obsolete Large beaked nose\n- Clinodactyly of the 2nd toe\n- Knee flexion contracture\n- Limited pronation\/supination of forearm\n- Microtia\n- Moderately short stature\n- Bronchitis\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Retrognathia\n- Facial asymmetry\n- Short chin\n- Sloping forehead\n- Micrognathia\n- Absent earlobe\n- Telecanthus\n- Proptosis\n- Dental crowding\n- Dental malocclusion\n- Atypical behavior\n- Abnormality of the hand\n- Brachydactyly\n- Intellectual disability\n- Intrauterine growth retardation\n- Small for gestational age\n- Abnormal foot morphology\n- Talipes equinovarus\n- Sandal gap\n- High, narrow palate\n- Abnormal respiratory system physiology\n- Recurrent bronchitis\n- Dislocated radial head\n- Hip contracture\n- obsolete Large beaked nose\n- Clinodactyly of the 5th finger\n- Knee dislocation\n- Clinodactyly of the 2nd toe\n- Knee flexion contracture\n- Microtia\n- Moderately short stature\n- Feeding difficulties in infancy\n- Pseudoepiphysis of the proximal phalanx of the 5th finger\n- Short finger\n- Pseudoepiphysis of the proximal phalanx of the 2nd finger\n- Carpal synostosis\n- Short palpebral fissure\n- Type I diabetes mellitus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/08036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n- Proptosis\n- Craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Hypertelorism\n- Single transverse palmar crease\n- Prominent fingertip pads\n- Global developmental delay\n- Sparse lateral eyebrow\n- Abnormal finger flexion crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hyperactivity\n- Intellectual disability\n- Global developmental delay\n- Bilateral cleft lip and palate\n- 2-3 toe syndactyly\n- Brain atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/08039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/08040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Prominent fingertip pads\n- Seizure\n- Umbilical hernia\n- Scoliosis\n- Prominent interphalangeal joints\n- Sparse hair\n- Moderate global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Delayed eruption of teeth\n- Widely spaced teeth\n- Prominent fingertip pads\n- Absent speech\n- Failure to thrive\n- Mitral regurgitation\n- Patent foramen ovale\n- Sandal gap\n- Facial hypertrichosis\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Ventricular septal hypertrophy\n- Sparse hair\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Delayed eruption of teeth\n- Widely spaced teeth\n- Prominent fingertip pads\n- Absent speech\n- Failure to thrive\n- Mitral regurgitation\n- Patent foramen ovale\n- Sandal gap\n- Facial hypertrichosis\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Ventricular septal hypertrophy\n- Sparse hair\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Delayed eruption of teeth\n- Widely spaced teeth\n- Prominent fingertip pads\n- Absent speech\n- Failure to thrive\n- Mitral regurgitation\n- Patent foramen ovale\n- Sandal gap\n- Facial hypertrichosis\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Ventricular septal hypertrophy\n- Sparse hair\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Narrow nasal bridge\n- Short toe\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent eyelashes\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Narrow nasal bridge\n- Short toe\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent eyelashes\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Narrow nasal bridge\n- Short toe\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent eyelashes\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Narrow nasal bridge\n- Short toe\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent eyelashes\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Narrow nasal bridge\n- Short toe\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Short metatarsal\n- Prominent eyelashes\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- Long philtrum\n- Downslanted palpebral fissures\n- Long eyelashes\n- Autistic behavior\n- Short attention span\n- Eczema\n- Seizure\n- Hypotonia\n- Absent speech\n- Coarctation of aorta\n- Short stature\n- Decreased body weight\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Feeding difficulties in infancy\n- Broad distal phalanx of finger\n- Severe global developmental delay\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Triangular face\n- Long philtrum\n- Downslanted palpebral fissures\n- Long eyelashes\n- Autistic behavior\n- Short attention span\n- Eczema\n- Seizure\n- Hypotonia\n- Absent speech\n- Coarctation of aorta\n- Short stature\n- Decreased body weight\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Feeding difficulties in infancy\n- Broad distal phalanx of finger\n- Severe global developmental delay\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Constipation\n- Abnormal hippocampus morphology\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, mild\n- Recurrent infections\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Joint hypermobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypotonia\n- Joint hypermobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypermetropia\n- Atypical behavior\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Joint hypermobility\n- Vomiting\n- Abnormal aggressive, impulsive or violent behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Hypotonia\n- Joint hypermobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/08059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Thin upper lip vermilion\n- Trigonocephaly\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Underdeveloped nasal alae\n- Blepharophimosis\n- Sparse eyelashes\n- Synophrys\n- Osteopenia\n- Tapered finger\n- Dysarthria\n- Drooling\n- Clumsiness\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Premature loss of teeth\n- Attention deficit hyperactivity disorder\n- Aplasia\/Hypoplasia of the nails\n- Cone-shaped epiphyses of the toes\n- Tented upper lip vermilion\n- Chin with horizontal crease\n- Overhanging nasal tip\n- Overweight\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Thin upper lip vermilion\n- Trigonocephaly\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Underdeveloped nasal alae\n- Blepharophimosis\n- Sparse eyelashes\n- Synophrys\n- Osteopenia\n- Tapered finger\n- Dysarthria\n- Drooling\n- Clumsiness\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Delayed skeletal maturation\n- Clinodactyly of the 5th finger\n- Premature loss of teeth\n- Attention deficit hyperactivity disorder\n- Aplasia\/Hypoplasia of the nails\n- Cone-shaped epiphyses of the toes\n- Tented upper lip vermilion\n- Chin with horizontal crease\n- Overhanging nasal tip\n- Overweight\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Thick eyebrow\n- Blepharophimosis\n- Widely spaced teeth\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Hypotonia\n- Plagiocephaly\n- Joint laxity\n- Small for gestational age\n- Frontal bossing\n- Gastroesophageal reflux\n- Difficulty walking\n- Spastic tetraplegia\n- Highly arched eyebrow\n- Scoliosis\n- Recurrent bronchitis\n- Limb joint contracture\n- Short nose\n- Recurrent pneumonia\n- Overlapping fingers\n- Aplastic\/hypoplastic toenail\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Flexion contracture of finger\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Thick eyebrow\n- Blepharophimosis\n- Widely spaced teeth\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Hypotonia\n- Plagiocephaly\n- Joint laxity\n- Small for gestational age\n- Frontal bossing\n- Gastroesophageal reflux\n- Difficulty walking\n- Spastic tetraplegia\n- Highly arched eyebrow\n- Scoliosis\n- Recurrent bronchitis\n- Limb joint contracture\n- Short nose\n- Recurrent pneumonia\n- Overlapping fingers\n- Aplastic\/hypoplastic toenail\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Flexion contracture of finger\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Thick eyebrow\n- Blepharophimosis\n- Widely spaced teeth\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Hypotonia\n- Plagiocephaly\n- Joint laxity\n- Small for gestational age\n- Frontal bossing\n- Gastroesophageal reflux\n- Difficulty walking\n- Spastic tetraplegia\n- Highly arched eyebrow\n- Scoliosis\n- Recurrent bronchitis\n- Limb joint contracture\n- Short nose\n- Recurrent pneumonia\n- Overlapping fingers\n- Aplastic\/hypoplastic toenail\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Flexion contracture of finger\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Thick eyebrow\n- Blepharophimosis\n- Widely spaced teeth\n- Atypical behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hirsutism\n- Seizure\n- Hypotonia\n- Plagiocephaly\n- Joint laxity\n- Small for gestational age\n- Frontal bossing\n- Gastroesophageal reflux\n- Difficulty walking\n- Spastic tetraplegia\n- Highly arched eyebrow\n- Scoliosis\n- Recurrent bronchitis\n- Limb joint contracture\n- Short nose\n- Recurrent pneumonia\n- Overlapping fingers\n- Aplastic\/hypoplastic toenail\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Flexion contracture of finger\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Short philtrum\n- Wide nasal bridge\n- Depressed nasal tip\n- Ptosis\n- Blepharophimosis\n- Sparse eyelashes\n- Arachnodactyly\n- Seizure\n- Hypotonia\n- Joint laxity\n- Sparse scalp hair\n- Highly arched eyebrow\n- Scoliosis\n- Agenesis of permanent teeth\n- Feeding difficulties in infancy\n- Moderate global developmental delay\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Narrow nasal ridge\n- Wide nasal bridge\n- Depressed nasal tip\n- Astigmatism\n- Blepharophimosis\n- Dental malocclusion\n- Low frustration tolerance\n- Enuresis\n- Tapered finger\n- Short foot\n- Frontal bossing\n- Short nose\n- Sagittal craniosynostosis\n- Enamel hypoplasia\n- Aplastic\/hypoplastic toenail\n- Moderate global developmental delay\n- Feeding difficulties\n- Flat face\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Narrow nasal ridge\n- Wide nasal bridge\n- Depressed nasal tip\n- Astigmatism\n- Blepharophimosis\n- Dental malocclusion\n- Low frustration tolerance\n- Enuresis\n- Tapered finger\n- Short foot\n- Frontal bossing\n- Short nose\n- Sagittal craniosynostosis\n- Enamel hypoplasia\n- Aplastic\/hypoplastic toenail\n- Moderate global developmental delay\n- Feeding difficulties\n- Flat face\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Narrow nasal ridge\n- Wide nasal bridge\n- Wide nose\n- Blepharophimosis\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Arachnodactyly\n- Pes planus\n- Hallux valgus\n- Frontal bossing\n- Sparse scalp hair\n- Highly arched eyebrow\n- Limb joint contracture\n- Short nose\n- Moderate global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Broad face\n- Epicanthus\n- Hypertelorism\n- Narrow nasal ridge\n- Wide nasal bridge\n- Wide nose\n- Blepharophimosis\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Arachnodactyly\n- Pes planus\n- Hallux valgus\n- Frontal bossing\n- Sparse scalp hair\n- Highly arched eyebrow\n- Limb joint contracture\n- Short nose\n- Moderate global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Broad face\n- Epicanthus\n- Long philtrum\n- Small earlobe\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Anteverted nares\n- Blepharophimosis\n- Sparse eyelashes\n- Abnormal repetitive mannerisms\n- Tapered finger\n- Hypotonia\n- Joint laxity\n- Pes planus\n- Frontal bossing\n- Sparse scalp hair\n- 2-3 toe syndactyly\n- Proximal placement of thumb\n- Anterior creases of earlobe\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Chin with horizontal crease\n- Flat face\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Blepharophimosis\n- Sparse eyelashes\n- Delayed speech and language development\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Pes planus\n- Frontal bossing\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Chiari malformation\n- Highly arched eyebrow\n- Short nose\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Hypoplasia of the pons\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Blepharophimosis\n- Sparse eyelashes\n- Delayed speech and language development\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Pes planus\n- Frontal bossing\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Chiari malformation\n- Highly arched eyebrow\n- Short nose\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Hypoplasia of the pons\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Blepharophimosis\n- Sparse eyelashes\n- Delayed speech and language development\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Pes planus\n- Frontal bossing\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Chiari malformation\n- Highly arched eyebrow\n- Short nose\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Hypoplasia of the pons\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Blepharophimosis\n- Sparse eyelashes\n- Delayed speech and language development\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Pes planus\n- Frontal bossing\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Chiari malformation\n- Highly arched eyebrow\n- Short nose\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Hypoplasia of the pons\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow nasal ridge\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Blepharophimosis\n- Sparse eyelashes\n- Delayed speech and language development\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Pes planus\n- Frontal bossing\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Chiari malformation\n- Highly arched eyebrow\n- Short nose\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Hypoplasia of the pons\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Low-set ears\n- Wide nasal bridge\n- Wide nose\n- Ptosis\n- Blepharophimosis\n- Sparse eyelashes\n- Widely spaced teeth\n- Tapered finger\n- Hypotonia\n- Frontal bossing\n- Highly arched eyebrow\n- Clinodactyly of the 5th finger\n- Aplastic\/hypoplastic toenail\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Chin with horizontal crease\n- Sparse eyebrow\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Long philtrum\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Blepharophimosis\n- Sparse eyelashes\n- Synophrys\n- Arachnodactyly\n- Hypotonia\n- Spastic tetraparesis\n- Plagiocephaly\n- Phimosis\n- Pes cavus\n- Ventriculomegaly\n- Drooling\n- Highly arched eyebrow\n- Recurrent bronchitis\n- Limb joint contracture\n- Secondary microcephaly\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Flexion contracture of finger\n- Abnormal ear morphology\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Long philtrum\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Blepharophimosis\n- Sparse eyelashes\n- Synophrys\n- Arachnodactyly\n- Hypotonia\n- Spastic tetraparesis\n- Plagiocephaly\n- Phimosis\n- Pes cavus\n- Ventriculomegaly\n- Drooling\n- Highly arched eyebrow\n- Recurrent bronchitis\n- Limb joint contracture\n- Secondary microcephaly\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Flexion contracture of finger\n- Abnormal ear morphology\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Long philtrum\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Blepharophimosis\n- Sparse eyelashes\n- Synophrys\n- Arachnodactyly\n- Hypotonia\n- Spastic tetraparesis\n- Plagiocephaly\n- Phimosis\n- Pes cavus\n- Ventriculomegaly\n- Drooling\n- Highly arched eyebrow\n- Recurrent bronchitis\n- Limb joint contracture\n- Secondary microcephaly\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Flexion contracture of finger\n- Abnormal ear morphology\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Long philtrum\n- Depressed nasal tip\n- Astigmatism\n- Hypermetropia\n- Blepharophimosis\n- Sparse eyelashes\n- Synophrys\n- Arachnodactyly\n- Hypotonia\n- Spastic tetraparesis\n- Plagiocephaly\n- Phimosis\n- Pes cavus\n- Ventriculomegaly\n- Drooling\n- Highly arched eyebrow\n- Recurrent bronchitis\n- Limb joint contracture\n- Secondary microcephaly\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Flexion contracture of finger\n- Abnormal ear morphology\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Long philtrum\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Wide nose\n- Blepharophimosis\n- Sparse eyelashes\n- Abnormal repetitive mannerisms\n- Hirsutism\n- Small for gestational age\n- Patent ductus arteriosus\n- Short distal phalanx of toe\n- Pulmonary arterial hypertension\n- Sparse scalp hair\n- Scoliosis\n- Decreased body weight\n- Short distal phalanx of finger\n- Severe global developmental delay\n- Abnormal ear morphology\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Long philtrum\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Depressed nasal tip\n- Wide nose\n- Blepharophimosis\n- Sparse eyelashes\n- Abnormal repetitive mannerisms\n- Hirsutism\n- Small for gestational age\n- Patent ductus arteriosus\n- Short distal phalanx of toe\n- Pulmonary arterial hypertension\n- Sparse scalp hair\n- Scoliosis\n- Decreased body weight\n- Short distal phalanx of finger\n- Severe global developmental delay\n- Abnormal ear morphology\n- Narrow palpebral fissure\n- Sparse eyebrow\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Long eyelashes\n- Hypermetropia\n- Esotropia\n- Blepharophimosis\n- Sparse eyelashes\n- Widely spaced teeth\n- Adrenal insufficiency\n- Hypotonia\n- Hip dysplasia\n- Bilateral talipes equinovarus\n- Highly arched eyebrow\n- Limb joint contracture\n- Supraventricular tachycardia\n- Swan neck-like deformities of the fingers\n- Chronic lung disease\n- Severe global developmental delay\n- Flexion contracture of finger\n- Diagonal earlobe crease\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Long eyelashes\n- Hypermetropia\n- Esotropia\n- Blepharophimosis\n- Sparse eyelashes\n- Widely spaced teeth\n- Adrenal insufficiency\n- Hypotonia\n- Hip dysplasia\n- Bilateral talipes equinovarus\n- Highly arched eyebrow\n- Limb joint contracture\n- Supraventricular tachycardia\n- Swan neck-like deformities of the fingers\n- Chronic lung disease\n- Severe global developmental delay\n- Flexion contracture of finger\n- Diagonal earlobe crease\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Long eyelashes\n- Hypermetropia\n- Blepharophimosis\n- Sparse eyelashes\n- Widely spaced teeth\n- Low frustration tolerance\n- Hypotonia\n- Hip dysplasia\n- Bilateral talipes equinovarus\n- Highly arched eyebrow\n- Limb joint contracture\n- Chronic lung disease\n- Severe global developmental delay\n- Camptodactyly\n- Flexion contracture of finger\n- Diagonal earlobe crease\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Wide nasal bridge\n- Anteverted nares\n- Long eyelashes\n- Hypermetropia\n- Blepharophimosis\n- Sparse eyelashes\n- Widely spaced teeth\n- Low frustration tolerance\n- Hypotonia\n- Hip dysplasia\n- Bilateral talipes equinovarus\n- Highly arched eyebrow\n- Limb joint contracture\n- Chronic lung disease\n- Severe global developmental delay\n- Camptodactyly\n- Flexion contracture of finger\n- Diagonal earlobe crease\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/08087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Downslanted palpebral fissures\n- Primary amenorrhea\n- Intellectual disability\n- Overgrowth\n- Patent ductus arteriosus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Downslanted palpebral fissures\n- Natal tooth\n- Global developmental delay\n- Specific learning disability\n- Overgrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Downslanted palpebral fissures\n- Abnormality of the frontal hairline\n- Global developmental delay\n- Frontal bossing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Hypertrichosis\n- Global developmental delay\n- Specific learning disability\n- Proportionate short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Myopia\n- Intellectual disability, mild\n- Joint laxity\n- Abnormality of speech or vocalization\n- Sparse scalp hair\n- Mild short stature\n- Short distal phalanx of the 5th finger\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Myopia\n- Intellectual disability, mild\n- Joint laxity\n- Abnormality of speech or vocalization\n- Sparse scalp hair\n- Mild short stature\n- Short distal phalanx of the 5th finger\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Myopia\n- Intellectual disability, mild\n- Joint laxity\n- Abnormality of speech or vocalization\n- Sparse scalp hair\n- Mild short stature\n- Short distal phalanx of the 5th finger\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Coarse facial features\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Myopia\n- Intellectual disability, mild\n- Joint laxity\n- Abnormality of speech or vocalization\n- Sparse scalp hair\n- Mild short stature\n- Short distal phalanx of the 5th finger\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Abnormal ear morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocele testis\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Delayed speech and language development\n- Intellectual disability\n- Abnormal corpus callosum morphology\n- Sparse scalp hair\n- Mild short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Thick nasal alae\n- Ivory epiphyses\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Abnormal ear morphology\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Hydrocele testis\n- Wide mouth\n- Macroglossia\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Wide nose\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Delayed speech and language development\n- Intellectual disability\n- Abnormal corpus callosum morphology\n- Sparse scalp hair\n- Mild short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Thick nasal alae\n- Ivory epiphyses\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Abnormal ear morphology\n- Decreased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Delayed speech and language development\n- Hyperactivity\n- Eczema\n- Hirsutism\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Sparse scalp hair\n- Depressed nasal bridge\n- Thick nasal alae\n- Ivory epiphyses\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Delayed speech and language development\n- Hyperactivity\n- Eczema\n- Hirsutism\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Sparse scalp hair\n- Depressed nasal bridge\n- Thick nasal alae\n- Ivory epiphyses\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Delayed speech and language development\n- Hyperactivity\n- Eczema\n- Hirsutism\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Sparse scalp hair\n- Depressed nasal bridge\n- Thick nasal alae\n- Ivory epiphyses\n- Hypoplastic fifth toenail\n- Feeding difficulties\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/08101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Hypermetropia\n- Anxiety\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Disproportionate tall stature\n- Sleep disturbance\n- Feeding difficulties in infancy\n- Hyperextensibility of the knee\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/08102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Short philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Autism\n- Intellectual disability, mild\n- Thick vermilion border\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/08103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Abnormal sternum morphology\n- Hyperpigmentation of the skin\n- Global developmental delay\n- Joint laxity\n- Disproportionate tall stature\n- Constipation\n- Sleep disturbance\n- Developmental regression\n- Long toe\n- Intellectual disability, severe\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/08104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High forehead\n- Global developmental delay\n- Sandal gap\n- Intellectual disability, moderate\n- Attention deficit hyperactivity disorder\n- Frequent temper tantrums\n- Tip-toe gait\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/08105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Anteverted nares\n- Downslanted palpebral fissures\n- Periorbital fullness\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Joint laxity\n- Asthma\n- Short nose\n- Sparse lateral eyebrow\n- Attention deficit hyperactivity disorder\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/08106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Hearing impairment\n- Thick eyebrow\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Intellectual disability, moderate\n- Developmental regression\n- Microtia\n- Short face\n- Athetoid cerebral palsy\n- Thick vermilion border\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/08107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Jaundice\n- Seizure\n- Intellectual disability, mild\n- Global developmental delay\n- Constipation\n- Cerebral atrophy\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Recurrent respiratory infections\n- EEG with polyspike wave complexes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/08108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macroglossia\n- Macrocephaly\n- Mandibular prognathia\n- Macrotia\n- Deeply set eye\n- Hypotelorism\n- Irritability\n- Tapered finger\n- Seizure\n- Intellectual disability, mild\n- Global developmental delay\n- Cerebellar hypoplasia\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Choroid plexus cyst\n- Enlarged cisterna magna\n- Delayed skeletal maturation\n- Low hanging columella\n- Unilateral cryptorchidism\n- Overweight\n- Sparse eyebrow\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/08109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Downslanted palpebral fissures\n- Widely spaced teeth\n- Autistic behavior\n- Hypotonia\n- Global developmental delay\n- Constipation\n- Bilateral tonic-clonic seizure\n- Apraxia\n- Developmental regression\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/08110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Deeply set eye\n- Proptosis\n- Dental malocclusion\n- Anxiety\n- Intellectual disability, mild\n- Motor delay\n- Hypernasal speech\n- Exaggerated cupid's bow\n- Sleep disturbance\n- Scoliosis\n- Enamel hypomineralization\n- Enamel hypoplasia\n- Prominent floating ribs\n- Axial hypotonia\n- Chin with vertical crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/08111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Low anterior hairline\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Hypotelorism\n- Pectus excavatum\n- Jaundice\n- Hypertrichosis\n- Arachnodactyly\n- Global developmental delay\n- Right ventricular hypertrophy\n- Talipes equinovarus\n- Recurrent respiratory infections\n- Neonatal respiratory distress\n- High, narrow palate\n- Hyperbilirubinemia\n- Tricuspid regurgitation\n- Progeroid facial appearance\n- Axial hypotonia\n- Metatarsus valgus\n- Muscular ventricular septal defect\n- Right bundle branch block\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Low anterior hairline\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Hypotelorism\n- Pectus excavatum\n- Jaundice\n- Hypertrichosis\n- Arachnodactyly\n- Global developmental delay\n- Right ventricular hypertrophy\n- Talipes equinovarus\n- Recurrent respiratory infections\n- Neonatal respiratory distress\n- High, narrow palate\n- Hyperbilirubinemia\n- Tricuspid regurgitation\n- Progeroid facial appearance\n- Axial hypotonia\n- Metatarsus valgus\n- Muscular ventricular septal defect\n- Right bundle branch block\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Low anterior hairline\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Hypotelorism\n- Pectus excavatum\n- Jaundice\n- Hypertrichosis\n- Arachnodactyly\n- Global developmental delay\n- Right ventricular hypertrophy\n- Talipes equinovarus\n- Recurrent respiratory infections\n- Neonatal respiratory distress\n- High, narrow palate\n- Hyperbilirubinemia\n- Tricuspid regurgitation\n- Progeroid facial appearance\n- Axial hypotonia\n- Metatarsus valgus\n- Muscular ventricular septal defect\n- Right bundle branch block\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Low anterior hairline\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Hypotelorism\n- Pectus excavatum\n- Jaundice\n- Hypertrichosis\n- Arachnodactyly\n- Global developmental delay\n- Right ventricular hypertrophy\n- Talipes equinovarus\n- Recurrent respiratory infections\n- Neonatal respiratory distress\n- High, narrow palate\n- Hyperbilirubinemia\n- Tricuspid regurgitation\n- Progeroid facial appearance\n- Axial hypotonia\n- Metatarsus valgus\n- Muscular ventricular septal defect\n- Right bundle branch block\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Low anterior hairline\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Hypotelorism\n- Pectus excavatum\n- Jaundice\n- Hypertrichosis\n- Arachnodactyly\n- Global developmental delay\n- Right ventricular hypertrophy\n- Talipes equinovarus\n- Recurrent respiratory infections\n- Neonatal respiratory distress\n- High, narrow palate\n- Hyperbilirubinemia\n- Tricuspid regurgitation\n- Progeroid facial appearance\n- Axial hypotonia\n- Metatarsus valgus\n- Muscular ventricular septal defect\n- Right bundle branch block\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Low anterior hairline\n- Low-set ears\n- Wide nasal bridge\n- Prominent nose\n- Hypotelorism\n- Pectus excavatum\n- Jaundice\n- Hypertrichosis\n- Arachnodactyly\n- Global developmental delay\n- Right ventricular hypertrophy\n- Talipes equinovarus\n- Recurrent respiratory infections\n- Neonatal respiratory distress\n- High, narrow palate\n- Hyperbilirubinemia\n- Tricuspid regurgitation\n- Progeroid facial appearance\n- Axial hypotonia\n- Metatarsus valgus\n- Muscular ventricular septal defect\n- Right bundle branch block\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Short philtrum\n- Hearing impairment\n- Thickened skin\n- Brachydactyly\n- Failure to thrive\n- Intrauterine growth retardation\n- Oligohydramnios\n- Patent ductus arteriosus\n- Ventriculomegaly\n- Scoliosis\n- Multiple joint contractures\n- Hip contracture\n- Short stature\n- Decreased body weight\n- Knee flexion contracture\n- Moderate global developmental delay\n- Morphological abnormality of the semicircular canal\n- Hypoplasia of the semicircular canal\n- Midface retrusion\n- Flexion contracture of finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Short philtrum\n- Hearing impairment\n- Thickened skin\n- Brachydactyly\n- Failure to thrive\n- Intrauterine growth retardation\n- Oligohydramnios\n- Patent ductus arteriosus\n- Ventriculomegaly\n- Scoliosis\n- Multiple joint contractures\n- Hip contracture\n- Short stature\n- Decreased body weight\n- Knee flexion contracture\n- Moderate global developmental delay\n- Morphological abnormality of the semicircular canal\n- Hypoplasia of the semicircular canal\n- Midface retrusion\n- Flexion contracture of finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Short philtrum\n- Hearing impairment\n- Thickened skin\n- Brachydactyly\n- Failure to thrive\n- Intrauterine growth retardation\n- Oligohydramnios\n- Patent ductus arteriosus\n- Ventriculomegaly\n- Scoliosis\n- Multiple joint contractures\n- Hip contracture\n- Short stature\n- Decreased body weight\n- Knee flexion contracture\n- Moderate global developmental delay\n- Morphological abnormality of the semicircular canal\n- Hypoplasia of the semicircular canal\n- Midface retrusion\n- Flexion contracture of finger\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Trismus\n- Mandibular prognathia\n- Short philtrum\n- Global developmental delay\n- Joint stiffness\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Bilateral camptodactyly\n- Unilateral ptosis\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Short philtrum\n- Single transverse palmar crease\n- Thickened skin\n- Brachydactyly\n- Intellectual disability, mild\n- Clinodactyly of the 5th finger\n- Short stature\n- High-frequency hearing impairment\n- Progressive flexion contractures\n- Bilateral cryptorchidism\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Short philtrum\n- Single transverse palmar crease\n- Thickened skin\n- Brachydactyly\n- Intellectual disability, mild\n- Clinodactyly of the 5th finger\n- Short stature\n- High-frequency hearing impairment\n- Progressive flexion contractures\n- Bilateral cryptorchidism\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Mandibular prognathia\n- Short philtrum\n- Single transverse palmar crease\n- Thickened skin\n- Brachydactyly\n- Intellectual disability, mild\n- Clinodactyly of the 5th finger\n- Short stature\n- High-frequency hearing impairment\n- Progressive flexion contractures\n- Bilateral cryptorchidism\n- Midface retrusion\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Short philtrum\n- Autistic behavior\n- Brachydactyly\n- Global developmental delay\n- Patent ductus arteriosus\n- Coarctation of aorta\n- Short stature\n- Decreased body weight\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Short philtrum\n- Autistic behavior\n- Brachydactyly\n- Global developmental delay\n- Patent ductus arteriosus\n- Coarctation of aorta\n- Short stature\n- Decreased body weight\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Short philtrum\n- Autistic behavior\n- Brachydactyly\n- Global developmental delay\n- Patent ductus arteriosus\n- Coarctation of aorta\n- Short stature\n- Decreased body weight\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low anterior hairline\n- Facial hypotonia\n- Wide nasal bridge\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Horizontal nystagmus\n- Seizure\n- Spasticity\n- Global developmental delay\n- Dystonia\n- Neonatal hypoglycemia\n- Intellectual disability, profound\n- Abnormal periventricular white matter morphology\n- Neonatal respiratory distress\n- Scoliosis\n- Abnormal respiratory system physiology\n- Secondary microcephaly\n- Inferior cerebellar vermis hypoplasia\n- Abnormal pyramidal sign\n- Bilateral cryptorchidism\n- Axial hypotonia\n- EEG with generalized slow activity\n- EEG with focal spike waves\n- Feeding difficulties\n- Brain atrophy\n- Delayed myelination\n- Neonatal bilateral asymmetric tonic seizure\n- Abnormality of movement\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydrocephalus\n- Broad forehead\n- Cutis marmorata\n- Hyperextensible skin\n- Abnormality of subcutaneous fat tissue\n- Nevus flammeus\n- Abnormal cerebellum morphology\n- Megalencephaly\n- Joint laxity\n- Large for gestational age\n- Toe syndactyly\n- Sandal gap\n- Polymicrogyria\n- Abnormality of the vasculature\n- Abnormality of connective tissue\n- 2-3 toe syndactyly\n- Thick corpus callosum\n- Polydactyly\n- Prominent forehead\n- Unilateral microphthalmos\n- Muscular ventricular septal defect\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydrocephalus\n- Broad forehead\n- Cutis marmorata\n- Hyperextensible skin\n- Abnormality of subcutaneous fat tissue\n- Nevus flammeus\n- Abnormal cerebellum morphology\n- Megalencephaly\n- Joint laxity\n- Large for gestational age\n- Toe syndactyly\n- Sandal gap\n- Polymicrogyria\n- Abnormality of the vasculature\n- Abnormality of connective tissue\n- 2-3 toe syndactyly\n- Thick corpus callosum\n- Polydactyly\n- Prominent forehead\n- Unilateral microphthalmos\n- Muscular ventricular septal defect\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydrocephalus\n- Broad forehead\n- Cutis marmorata\n- Hyperextensible skin\n- Abnormality of subcutaneous fat tissue\n- Nevus flammeus\n- Abnormal cerebellum morphology\n- Megalencephaly\n- Joint laxity\n- Large for gestational age\n- Toe syndactyly\n- Sandal gap\n- Polymicrogyria\n- Abnormality of the vasculature\n- Abnormality of connective tissue\n- 2-3 toe syndactyly\n- Thick corpus callosum\n- Polydactyly\n- Prominent forehead\n- Unilateral microphthalmos\n- Muscular ventricular septal defect\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Abnormal retinal morphology\n- Reduced eye contact\n- Absent speech\n- Hypoplasia of the corpus callosum\n- Generalized-onset seizure\n- Limb hypertonia\n- Kyphosis\n- Mild short stature\n- Focal-onset seizure\n- Axial hypotonia\n- Multifocal epileptiform discharges\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Full cheeks\n- Round face\n- Narrow forehead\n- Short neck\n- Reduced eye contact\n- Hand clenching\n- Seizure\n- Hypotonia\n- Spasticity\n- Neonatal hypotonia\n- Myoclonus\n- Absent speech\n- Decreased fetal movement\n- Frontal bossing\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Hypokinesia\n- Scoliosis\n- Respiratory failure\n- Focal-onset seizure\n- EEG with occipital focal spikes\n- Widened subarachnoid space\n- Profound global developmental delay\n- Arm dystonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Seizure\n- Generalized hypotonia\n- Absent speech\n- Talipes equinovarus\n- Cerebral atrophy\n- Asthma\n- Status epilepticus\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Hypokinesia\n- Corpus callosum atrophy\n- EEG with abnormally slow frequencies\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Reduced eye contact\n- Jaundice\n- Seizure\n- Hypertonia\n- Absent speech\n- Brisk reflexes\n- Hypokinesia\n- Scoliosis\n- Involuntary movements\n- Epileptic spasm\n- Feeding difficulties\n- Infantile spasms\n- Profound global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypotonia\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Status epilepticus\n- Scoliosis\n- Aspiration pneumonia\n- Profound global developmental delay\n- Fetal distress\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow forehead\n- Upslanted palpebral fissure\n- Abnormality of visual evoked potentials\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Absent speech\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Hypokinesia\n- Hypsarrhythmia\n- Atrophy\/Degeneration affecting the brainstem\n- Corpus callosum atrophy\n- Uplifted earlobe\n- Epileptic spasm\n- Delayed myelination\n- Infantile spasms\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Narrow forehead\n- Upslanted palpebral fissure\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Plagiocephaly\n- Hypokinesia\n- Uplifted earlobe\n- Feeding difficulties\n- Infantile spasms\n- Lateral ventricular asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Reduced eye contact\n- Absent speech\n- Lower limb spasticity\n- Focal clonic seizure\n- Hypokinesia\n- Scoliosis\n- Upper limb spasticity\n- Axial hypotonia\n- Multifocal epileptiform discharges\n- Dialeptic seizure\n- Severe global developmental delay\n- EEG with temporal focal spikes\n- Myoclonic seizure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Reduced eye contact\n- Seizure\n- Absent speech\n- Lower limb spasticity\n- Focal clonic seizure\n- Hypokinesia\n- Scoliosis\n- Upper limb spasticity\n- Axial hypotonia\n- Dialeptic seizure\n- Severe global developmental delay\n- EEG with temporal focal spikes\n- Myoclonic seizure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Mask-like facies\n- Round face\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Spasticity\n- Absent speech\n- Plagiocephaly\n- Cerebral atrophy\n- Hypokinesia\n- Scoliosis\n- Multifocal epileptiform discharges\n- Focal tonic seizure\n- Severe global developmental delay\n- Periventricular white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Mask-like facies\n- Round face\n- Reduced eye contact\n- Seizure\n- Hypotonia\n- Spasticity\n- Absent speech\n- Plagiocephaly\n- Cerebral atrophy\n- Hypokinesia\n- Scoliosis\n- Multifocal epileptiform discharges\n- Focal tonic seizure\n- Severe global developmental delay\n- Periventricular white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Facial hypotonia\n- Round face\n- Short neck\n- Optic disc pallor\n- Spastic tetraparesis\n- Cerebellar vermis hypoplasia\n- Dystonia\n- Brisk reflexes\n- Failure to thrive\n- Bilateral talipes equinovarus\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Clonus\n- Hypokinesia\n- Congenital contracture\n- Multiple joint contractures\n- Axial hypotonia\n- EEG with burst suppression\n- Feeding difficulties\n- Brain atrophy\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/08145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Abnormal sternum morphology\n- Large for gestational age\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Impaired social interactions\n- Intellectual disability, moderate\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Aggressive behavior\n- Hypotonia\n- Intellectual disability, mild\n- Craniosynostosis\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Macrotia\n- Autistic behavior\n- Hypotonia\n- Intellectual disability, mild\n- Polyhydramnios\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Autistic behavior\n- Hypotonia\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Aggressive behavior\n- Hypotonia\n- Intellectual disability, mild\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Cutis marmorata\n- Iris atrophy\n- Pes planus\n- Intellectual disability, moderate\n- Scoliosis\n- Fibrosarcoma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Autistic behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Retrognathia\n- Autistic behavior\n- Hypothyroidism\n- Intellectual disability, mild\n- Pyloric stenosis\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Autistic behavior\n- Seizure\n- Large for gestational age\n- Intellectual disability, moderate\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Impaired social interactions\n- Intellectual disability, mild\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Glabellar hemangioma\n- Hypotonia\n- Umbilical hernia\n- Intellectual disability, moderate\n- Accelerated skeletal maturation\n- Premature loss of primary teeth\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Psychosis\n- Autistic behavior\n- Hypotonia\n- Obesity\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Atypical behavior\n- Lack of spontaneous play\n- Irritability\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Global developmental delay\n- Specific learning disability\n- Overgrowth\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Attention deficit hyperactivity disorder\n- Brain atrophy\n- Halitosis\n- Congenital hydrocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/08159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Autism\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Reduced eye contact\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Overgrowth\n- Constipation\n- Gastroesophageal reflux\n- Repetitive compulsive behavior\n- Anal fissure\n- Brain atrophy\n- Overweight\n- Halitosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/08160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Small face\n- Mandibular prognathia\n- Triangular face\n- Prominent supraorbital ridges\n- Low-set, posteriorly rotated ears\n- Prominent nasal bridge\n- Prominent nose\n- Triangular nasal tip\n- Broad nasal tip\n- Anteverted nares\n- Webbed neck\n- Downslanted palpebral fissures\n- Agitation\n- Aggressive behavior\n- Compulsive behaviors\n- Autistic behavior\n- Anxiety\n- Syndactyly\n- Broad palm\n- Global developmental delay\n- Hypernasal speech\n- High pitched voice\n- Broad nail\n- Bilateral tonic-clonic seizure\n- Orofacial dyskinesia\n- Short palm\n- Rhizomelic arm shortening\n- Unilateral chest hypoplasia\n- Severe expressive language delay\n- Short finger\n- Short thumb\n- Short distal phalanx of finger\n- Echolalia\n- Prominent forehead\n- Mild receptive language delay\n- Broad chin\n- Skin-picking\n- Hair-pulling\n- Manifestations of perseverative thought or action\n- Separation insecurity\n- Insomnia\n- Idiosyncratic language\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/08161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Open mouth\n- Macrocephaly\n- Pointed chin\n- Long philtrum\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Ptosis\n- Autism\n- Abnormal repetitive mannerisms\n- Short attention span\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Clumsiness\n- Echolalia\n- Pica\n- Frequent temper tantrums\n- Reduced production of gestures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/08162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Otitis media\n- Widely spaced teeth\n- Autism\n- Aggressive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Irritability\n- Delayed speech and language development\n- Reduced eye contact\n- Global developmental delay\n- Motor delay\n- Gastroesophageal reflux\n- Pneumonia\n- Attention deficit hyperactivity disorder\n- Repetitive compulsive behavior\n- Hair-pulling\n- Frequent temper tantrums\n- Severe temper tantrums\n- obsolete Toe walking\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Tall stature\n- Wide mouth\n- Macroglossia\n- High palate\n- Macrocephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Long philtrum\n- Abnormal pinna morphology\n- Macrotia\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Hypermetropia\n- Thick eyebrow\n- Long palpebral fissure\n- Dental crowding\n- Eruption failure\n- Autistic behavior\n- Delayed speech and language development\n- Reduced eye contact\n- Large hands\n- Intellectual disability, mild\n- Motor delay\n- Hepatosplenomegaly\n- Large for gestational age\n- Umbilical hernia\n- Pes planus\n- Long foot\n- Short columella\n- Hypoglycemic seizures\n- Poor speech\n- Highly arched eyebrow\n- Short nose\n- Advanced eruption of teeth\n- Dimple chin\n- Supernumerary tooth\n- Linear earlobe crease\n- Bradyphrenia\n- Anteverted ears\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Tall stature\n- Wide mouth\n- Macroglossia\n- High palate\n- Macrocephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Long philtrum\n- Abnormal pinna morphology\n- Macrotia\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Hypermetropia\n- Thick eyebrow\n- Long palpebral fissure\n- Dental crowding\n- Eruption failure\n- Autistic behavior\n- Delayed speech and language development\n- Reduced eye contact\n- Large hands\n- Intellectual disability, mild\n- Motor delay\n- Hepatosplenomegaly\n- Large for gestational age\n- Umbilical hernia\n- Pes planus\n- Long foot\n- Short columella\n- Hypoglycemic seizures\n- Poor speech\n- Highly arched eyebrow\n- Short nose\n- Advanced eruption of teeth\n- Dimple chin\n- Supernumerary tooth\n- Linear earlobe crease\n- Bradyphrenia\n- Anteverted ears\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Tall stature\n- Wide mouth\n- Macroglossia\n- High palate\n- Macrocephaly\n- Long face\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Long philtrum\n- Abnormal pinna morphology\n- Macrotia\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Hypermetropia\n- Thick eyebrow\n- Long palpebral fissure\n- Dental crowding\n- Eruption failure\n- Autistic behavior\n- Delayed speech and language development\n- Reduced eye contact\n- Large hands\n- Intellectual disability, mild\n- Motor delay\n- Hepatosplenomegaly\n- Large for gestational age\n- Umbilical hernia\n- Pes planus\n- Long foot\n- Short columella\n- Hypoglycemic seizures\n- Poor speech\n- Highly arched eyebrow\n- Short nose\n- Advanced eruption of teeth\n- Dimple chin\n- Supernumerary tooth\n- Linear earlobe crease\n- Bradyphrenia\n- Anteverted ears\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/08166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal cyst\n- Narrow palate\n- High palate\n- Abnormality of the philtrum\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Cutis marmorata\n- Hand polydactyly\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n- Hemihypertrophy\n- Redundant skin\n- Toe syndactyly\n- Sandal gap\n- Neonatal hypoglycemia\n- Abnormality of the vasculature\n- Finger syndactyly\n- Dilation of Virchow-Robin spaces\n- Lateral ventricular asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Sloping forehead\n- Prominent nasal bridge\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Myopia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability, mild\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Sloping forehead\n- Prominent nasal bridge\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Myopia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability, mild\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Global developmental delay\n- Toe syndactyly\n- Sandal gap\n- Polymicrogyria\n- Hemifacial hypertrophy\n- Thick corpus callosum\n- Chiari type I malformation\n- Hemimegalencephaly\n- Hemihypertrophy of lower limb\n- Hemihypertrophy of upper limb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Syndactyly\n- Global developmental delay\n- Overgrowth\n- Scoliosis\n- Syringomyelia\n- Macrodactyly\n- Hemifacial hypertrophy\n- Thick corpus callosum\n- Chiari type I malformation\n- Hemimegalencephaly\n- Epidermal nevus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Compulsive behaviors\n- Hypotonia\n- Global developmental delay\n- Large for gestational age\n- Polymicrogyria\n- Abnormal cerebral white matter morphology\n- Hemifacial hypertrophy\n- Attention deficit hyperactivity disorder\n- Thick corpus callosum\n- Vascular skin abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Seizure\n- Hypotonia\n- Abnormal corpus callosum morphology\n- Absent speech\n- Large for gestational age\n- Ventriculomegaly\n- Polymicrogyria\n- Intellectual disability, profound\n- Abnormal cerebral white matter morphology\n- Cerebral dysmyelination\n- Vascular skin abnormality\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Cutis marmorata\n- Hypotonia\n- Large for gestational age\n- Ventriculomegaly\n- Polymicrogyria\n- Abnormal cerebral white matter morphology\n- Hemifacial hypertrophy\n- Thick corpus callosum\n- Focal-onset seizure\n- 3-4 toe syndactyly\n- Vascular skin abnormality\n- Moderate global developmental delay\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydrocephalus\n- Macrocephaly\n- Cutis marmorata\n- Hypotonia\n- Large for gestational age\n- Ventriculomegaly\n- Polymicrogyria\n- Abnormal cerebral white matter morphology\n- Hemifacial hypertrophy\n- Thick corpus callosum\n- Focal-onset seizure\n- 3-4 toe syndactyly\n- Vascular skin abnormality\n- Moderate global developmental delay\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/08176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Trigonocephaly\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Hypertelorism\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Coloboma\n- Short attention span\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Pachygyria\n- Broad nail\n- Ventriculomegaly\n- Highly arched eyebrow\n- Short stature\n- Thick corpus callosum\n- Congenital ptosis\n- Microtia\n- Dilation of Virchow-Robin spaces\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/08178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Astigmatism\n- Autism\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n- Developmental regression\n- Periventricular leukomalacia\n- Oppositional defiant disorder\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/08179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Astigmatism\n- Autism\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n- Developmental regression\n- Periventricular leukomalacia\n- Oppositional defiant disorder\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/08180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Astigmatism\n- Autism\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n- Developmental regression\n- Periventricular leukomalacia\n- Oppositional defiant disorder\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/08181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/08182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autistic behavior\n- Anxiety\n- Intellectual disability\n- Absent speech\n- Hyperventilation\n- Severe global developmental delay\n- Self-biting\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Hearing impairment\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Strabismus\n- Synophrys\n- Autism\n- Delayed speech and language development\n- Precocious puberty\n- Seizure\n- Global developmental delay\n- Motor delay\n- Macrodontia\n- Large forehead\n- Mild short stature\n- obsolete Prominent epicanthal folds\n- Chronic constipation\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Short chin\n- Prominent nasal bridge\n- Astigmatism\n- Long eyelashes\n- Thick eyebrow\n- Nystagmus\n- Autism\n- Delayed speech and language development\n- Sacral dimple\n- Neonatal hypotonia\n- Macrodontia\n- Pes planus\n- Mild short stature\n- Prominent nasal tip\n- Repetitive compulsive behavior\n- Moderate global developmental delay\n- Ankle clonus\n- Chronic fatigue\n- Clinodactyly\n- Periauricular skin pits\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Retrognathia\n- Triangular face\n- Wide nasal bridge\n- Anteverted nares\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Failure to thrive\n- Macrodontia\n- Bicuspid aortic valve\n- Patent foramen ovale\n- Large fleshy ears\n- High, narrow palate\n- Short stature\n- Feeding difficulties in infancy\n- Ankyloglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Broad nasal tip\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Anxiety\n- Dry skin\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Macrodontia\n- Pes planus\n- Iron deficiency anemia\n- Vomiting\n- Gastroesophageal reflux\n- Migraine\n- Sleep disturbance\n- Shuffling gait\n- Abnormal aggressive, impulsive or violent behavior\n- Attention deficit hyperactivity disorder\n- Subcortical white matter calcifications\n- Abnormality of the palpebral fissures\n- Philtrum with midline raphe\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Broad nasal tip\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Anxiety\n- Dry skin\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait disturbance\n- Macrodontia\n- Pes planus\n- Iron deficiency anemia\n- Vomiting\n- Gastroesophageal reflux\n- Migraine\n- Sleep disturbance\n- Shuffling gait\n- Abnormal aggressive, impulsive or violent behavior\n- Attention deficit hyperactivity disorder\n- Subcortical white matter calcifications\n- Abnormality of the palpebral fissures\n- Philtrum with midline raphe\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Oxycephaly\n- Hypertelorism\n- Convex nasal ridge\n- Strabismus\n- Visual impairment\n- Proptosis\n- Exotropia\n- Shallow orbits\n- Craniosynostosis\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Increased intracranial pressure\n- Obstructive sleep apnea\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Increased intracranial pressure\n- Obstructive sleep apnea\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Increased intracranial pressure\n- Obstructive sleep apnea\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Increased intracranial pressure\n- Obstructive sleep apnea\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Increased intracranial pressure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hydrocephalus\n- Retrognathia\n- Hypertelorism\n- Micrognathia\n- Convex nasal ridge\n- Proptosis\n- Pectus excavatum\n- Intellectual disability\n- Seizure\n- Subglottic stenosis\n- Language impairment\n- Thickened calvaria\n- Decreased body weight\n- Coronal craniosynostosis\n- Posterior fossa cyst\n- Sleep apnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypoplasia of the maxilla\n- Abnormality of the choanae\n- Proptosis\n- Toe syndactyly\n- Respiratory distress\n- Coronal craniosynostosis\n- Cutaneous finger syndactyly\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Mandibular prognathia\n- Hypertelorism\n- Low-set ears\n- Proptosis\n- Sacral dimple\n- Pallor\n- Seizure\n- Sandal gap\n- Anemia\n- Fever\n- Leukocytosis\n- Respiratory distress\n- Elbow ankylosis\n- Coronal craniosynostosis\n- Widely patent sagittal suture\n- Hallux varus\n- Broad hallux\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Dolichocephaly\n- Hypertelorism\n- Proptosis\n- Brachydactyly\n- Intrauterine growth retardation\n- Broad toe\n- Deviation of the thumb\n- Symphalangism affecting the phalanges of the hand\n- Symphalangism affecting the phalanges of the toes\n- Broad thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Hypertelorism\n- Strabismus\n- Proptosis\n- 2-3 finger syndactyly\n- Delayed closure of the anterior fontanelle\n- Short toe\n- Depressed nasal bridge\n- Short finger\n- Deviation of the thumb\n- Finger symphalangism\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Antepartum hemorrhage\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Hypertelorism\n- Strabismus\n- Proptosis\n- 2-3 finger syndactyly\n- Delayed closure of the anterior fontanelle\n- Short toe\n- Depressed nasal bridge\n- Short finger\n- Deviation of the thumb\n- Finger symphalangism\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Antepartum hemorrhage\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Hypertelorism\n- Strabismus\n- Proptosis\n- 2-3 finger syndactyly\n- Delayed closure of the anterior fontanelle\n- Short toe\n- Depressed nasal bridge\n- Short finger\n- Deviation of the thumb\n- Finger symphalangism\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Antepartum hemorrhage\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Proptosis\n- Brachydactyly\n- Hallux valgus\n- Broad toe\n- 2-3 toe syndactyly\n- Deviation of the thumb\n- Finger symphalangism\n- Broad thumb\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Conductive hearing impairment\n- Choanal stenosis\n- Proptosis\n- Brachydactyly\n- Motor delay\n- Increased intracranial pressure\n- Abnormality of the skull base\n- Upper airway obstruction\n- Obstructive sleep apnea\n- Respiratory failure\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Prolonged neonatal jaundice\n- Broad hallux\n- Abnormality of the nasal cavity\n- Abnormal hair whorl\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Respiratory tract infection\n- Snoring\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Brachyturricephaly\n- Facial hemangioma\n- Low-set ears\n- Downslanted palpebral fissures\n- Proptosis\n- Limited elbow extension\n- Omphalocele\n- Subglottic stenosis\n- Patent ductus arteriosus\n- Hydrops fetalis\n- Respiratory insufficiency\n- Polymicrogyria\n- Cerebral edema\n- Hepatomegaly\n- Intestinal malrotation\n- Downturned corners of mouth\n- Upper airway obstruction\n- Prune belly\n- Hepatic calcification\n- Nevus flammeus of the forehead\n- Broad hallux\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Low APGAR score\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/08223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hydrocephalus\n- Hypertelorism\n- Ptosis\n- Proptosis\n- Shallow orbits\n- Carious teeth\n- Increased intracranial pressure\n- Craniofacial dysostosis\n- Enamel hypomineralization\n- Prominent forehead\n- Abnormality of upper lip vermillion\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Trigonocephaly\n- Mandibular prognathia\n- Hypertelorism\n- Proptosis\n- Shallow orbits\n- Dental malocclusion\n- Abnormally large globe\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Malar flattening\n- Hypertelorism\n- Hypoplasia of the maxilla\n- Proptosis\n- Dental crowding\n- Anterior open-bite malocclusion\n- Copper beaten skull\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Apnea\n- Headache\n- Episodic vomiting\n- Abnormal respiratory system physiology\n- Obstructive sleep apnea\n- Craniofacial asymmetry\n- Anterior open-bite malocclusion\n- Midface retrusion\n- Abnormality of the maxillary sinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Hypoplasia of the maxilla\n- Proptosis\n- Papilledema\n- Craniosynostosis\n- Increased intracranial pressure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Sinusitis\n- Mastoiditis\n- Dolichocephaly\n- Hypertelorism\n- Proptosis\n- Abnormal skull morphology\n- Frontal bossing\n- Ventriculomegaly\n- Deviated nasal septum\n- Craniofacial dysostosis\n- Sagittal craniosynostosis\n- Airway obstruction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Short upper lip\n- Bifid uvula\n- High palate\n- Dolichocephaly\n- Mandibular prognathia\n- Hypertelorism\n- Long philtrum\n- Strabismus\n- Optic atrophy\n- Carious teeth\n- Dental malocclusion\n- Abnormal calvaria morphology\n- Deviated nasal septum\n- Depressed nasal bridge\n- Peg-shaped maxillary lateral incisors\n- Abnormality of primary molar morphology\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/08230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Gingival overgrowth\n- Downslanted palpebral fissures\n- Carious teeth\n- Widely spaced teeth\n- Microdontia\n- Hypoparathyroidism\n- Intellectual disability, mild\n- Obesity\n- Hypernasal speech\n- Thrombocytopenia\n- Scoliosis\n- Hypocalcemia\n- Hyperphosphatemia\n- EEG with spike-wave complexes\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Truncus arteriosus\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Full cheeks\n- Broad forehead\n- Long philtrum\n- Prominent nasal tip\n- Upper eyelid edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Strabismus\n- Blue irides\n- Protruding tongue\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/08236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Epicanthus\n- Microretrognathia\n- Round face\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Wide nose\n- Anteverted nares\n- Telecanthus\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Malar flattening\n- Low anterior hairline\n- Small forehead\n- Recurrent otitis media\n- Protruding ear\n- Bulbous nose\n- Underdeveloped nasal alae\n- Upslanted palpebral fissure\n- Carious teeth\n- Anxiety\n- Delayed speech and language development\n- Abnormality of the vertebral column\n- Sacral dimple\n- Motor delay\n- Weak cry\n- Pulmonic stenosis\n- Gastroesophageal reflux\n- Scoliosis\n- Recurrent upper respiratory tract infections\n- Deviated nasal septum\n- 2-3 toe syndactyly\n- Enamel hypoplasia\n- Nasal regurgitation\n- Feeding difficulties\n- Heart murmur\n- Manifestations of perseverative thought or action\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Macrotia\n- Protruding ear\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Long face\n- Facial asymmetry\n- Protruding ear\n- Hypotelorism\n- Large forehead\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Long face\n- Facial asymmetry\n- Protruding ear\n- Hypotelorism\n- Large forehead\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocele testis\n- Macroorchidism\n- Macrotia\n- Reduced eye contact\n- Soft skin\n- Large forehead\n- Sparse body hair\n- Eunuchoid habitus\n- Abnormal jaw morphology\n- Decreased head circumference\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Long face\n- Aggressive behavior\n- Anxiety\n- Overlapping toe\n- Long hallux\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Sleep disturbance\n- Wide intermamillary distance\n- Attached earlobe\n- Broad hallux\n- Broad columella\n- Everted upper lip vermilion\n- Thick vermilion border\n- Wide nasal base\n- Shyness\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Abnormal nasal bridge morphology\n- Short attention span\n- Anxiety\n- Delayed speech and language development\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Joint laxity\n- Abnormal social behavior\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Menorrhagia\n- Mandibular prognathia\n- Cupped ear\n- Recurrent otitis media\n- Strabismus\n- Esotropia\n- Carious teeth\n- Microdontia\n- Anxiety\n- Reduced eye contact\n- Cafe-au-lait spot\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Low posterior hairline\n- High, narrow palate\n- Hypoplasia of the radius\n- Hypoplasia of the ulna\n- Mesomelia\n- Short stature\n- Hyperextensible thumb\n- Attention deficit hyperactivity disorder\n- Vertebral wedging\n- Short 4th metacarpal\n- Short 5th metacarpal\n- Recurrent hand flapping\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Coarse facial features\n- Broad forehead\n- High forehead\n- Macrotia\n- Global developmental delay\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/08256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Strabismus\n- Impaired social interactions\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Motor delay\n- Bilateral tonic-clonic seizure\n- Intellectual disability, moderate\n- Hemifacial hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Drooling\n- Myoclonic absence seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Impaired social interactions\n- Delayed speech and language development\n- Hypotonia\n- Motor delay\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Short chin\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Thick eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short chin\n- Anteverted nares\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short philtrum\n- Short chin\n- Anteverted nares\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short chin\n- Anteverted nares\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Short philtrum\n- Anteverted nares\n- Thick eyebrow\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short chin\n- Anteverted nares\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short chin\n- Anteverted nares\n- Thick eyebrow\n- Exaggerated cupid's bow\n- Prominent nasal tip\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Anteverted nares\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Hypertelorism\n- Thick eyebrow\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Anteverted nares\n- Thick eyebrow\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short philtrum\n- Short chin\n- Anteverted nares\n- Exaggerated cupid's bow\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Short chin\n- Anteverted nares\n- Thick eyebrow\n- Large forehead\n- Prominent nasal tip\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Short chin\n- Thick eyebrow\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short chin\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short philtrum\n- Short chin\n- Anteverted nares\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Anteverted nares\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Short chin\n- Thick eyebrow\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Short philtrum\n- Thick eyebrow\n- Exaggerated cupid's bow\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short chin\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick eyebrow\n- Widely-spaced maxillary central incisors\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Anteverted nares\n- Widely spaced teeth\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short chin\n- Widely spaced teeth\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short chin\n- Prominent nose\n- Thick eyebrow\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Short chin\n- Anteverted nares\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short chin\n- Thick eyebrow\n- Widely spaced teeth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Short philtrum\n- Anteverted nares\n- Widely spaced teeth\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- Short philtrum\n- Short chin\n- Anteverted nares\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Wide nasal bridge\n- Aggressive behavior\n- Gastroesophageal reflux\n- Unsteady gait\n- Intellectual disability, moderate\n- Sleep disturbance\n- Long nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Wide nasal bridge\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Jaundice\n- Cafe-au-lait spot\n- Seizure\n- Hypotonia\n- Hip dysplasia\n- Constipation\n- Broad-based gait\n- Intellectual disability, moderate\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Myoclonic absence seizure\n- Nasogastric tube feeding in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Wide nasal bridge\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Global developmental delay\n- Pes planus\n- Constipation\n- Broad-based gait\n- Intellectual disability, moderate\n- Sleep disturbance\n- Long nose\n- Microtia\n- Atonic seizure\n- Myoclonic absence seizure\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Wide nasal bridge\n- Nystagmus\n- Aggressive behavior\n- Compulsive behaviors\n- Autistic behavior\n- Pectus excavatum\n- Hirsutism\n- Hypotonia\n- Hip dysplasia\n- Constipation\n- Generalized non-motor (absence) seizure\n- Intellectual disability, moderate\n- Sleep disturbance\n- Kyphosis\n- Long nose\n- Atonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Protruding ear\n- Aggressive behavior\n- Compulsive behaviors\n- Autistic behavior\n- Hyperpigmentation of the skin\n- Cafe-au-lait spot\n- Hypotonia\n- Pes planus\n- Gastroesophageal reflux\n- Recurrent respiratory infections\n- Clumsiness\n- Intellectual disability, moderate\n- Sleep disturbance\n- Feeding difficulties in infancy\n- Head-banging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Aggressive behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hirsutism\n- Tapered finger\n- Global developmental delay\n- Constipation\n- Gait ataxia\n- Broad-based gait\n- Intellectual disability, moderate\n- Sleep disturbance\n- Long nose\n- Obsessive-compulsive trait\n- Visually-induced seizure\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Facial hypotonia\n- Prominent nasal bridge\n- Deeply set eye\n- Autistic behavior\n- Inflexible adherence to routines or rituals\n- Reduced eye contact\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Absent speech\n- Gastroesophageal reflux\n- Lower limb spasticity\n- Gait ataxia\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Broad-based gait\n- Drooling\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Kyphoscoliosis\n- Periventricular leukomalacia\n- Axial hypotonia\n- Abnormal columella morphology\n- Atonic seizure\n- Intellectual disability, severe\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Facial hypotonia\n- Prominent nasal bridge\n- Deeply set eye\n- Autistic behavior\n- Inflexible adherence to routines or rituals\n- Reduced eye contact\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Absent speech\n- Growth delay\n- Gastroesophageal reflux\n- Lower limb spasticity\n- Gait ataxia\n- Bilateral tonic-clonic seizure\n- Generalized non-motor (absence) seizure\n- Drooling\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Kyphoscoliosis\n- Short stature\n- Decreased body weight\n- Feeding difficulties in infancy\n- Abnormal columella morphology\n- Atonic seizure\n- Intellectual disability, severe\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/08296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Seizure\n- Cerebral atrophy\n- Bilateral tonic-clonic seizure\n- Hypsarrhythmia\n- Recurrent pneumonia\n- Motor regression\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/08297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Developmental regression\n- Abnormal head movements\n- Focal-onset seizure\n- Neck muscle hypertrophy\n- Multifocal seizures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/08298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Reduced eye contact\n- Seizure\n- Gait disturbance\n- Short foot\n- Sleep disturbance\n- Developmental regression\n- Kyphoscoliosis\n- Bruxism\n- Short palm\n- EEG with focal spikes\n- Mild global developmental delay\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/08299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Reduced eye contact\n- Seizure\n- Gait disturbance\n- Short foot\n- Sleep disturbance\n- Developmental regression\n- Kyphoscoliosis\n- Bruxism\n- Short palm\n- EEG with focal spikes\n- Mild global developmental delay\n- Tonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/08300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Microcephaly\n- Round face\n- Square face\n- Bulbous nose\n- Strabismus\n- Telecanthus\n- Delayed speech and language development\n- Seizure\n- Spasticity\n- Motor delay\n- Spastic tetraparesis\n- Plagiocephaly\n- Growth delay\n- Small for gestational age\n- Patent ductus arteriosus\n- Talipes equinovarus\n- Large forehead\n- Dysphagia\n- Constipation\n- Status epilepticus\n- Nail dysplasia\n- Highly arched eyebrow\n- Radioulnar synostosis\n- Prominent metopic ridge\n- Aplasia\/Hypoplasia of the patella\n- Severe intrauterine growth retardation\n- Axial hypotonia\n- Intellectual disability, severe\n- Finger clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/08301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Full cheeks\n- Round face\n- Square face\n- Low-set ears\n- Abnormal pinna morphology\n- Bulbous nose\n- Epistaxis\n- Strabismus\n- Telecanthus\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Ataxia\n- Motor delay\n- Growth delay\n- Small for gestational age\n- Large forehead\n- Dysphagia\n- Bilateral tonic-clonic seizure\n- Asthma\n- Nail dysplasia\n- Delayed CNS myelination\n- Highly arched eyebrow\n- Abnormality of the radial head\n- Abnormality of radial diaphysis\n- Aplasia\/Hypoplasia of the patella\n- Cerebellar vermis atrophy\n- Abnormality of the palpebral fissures\n- Axial hypotonia\n- Bilateral coxa valga\n- EEG with spike-wave complexes (<2.5 Hz)\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/08302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Full cheeks\n- Round face\n- Square face\n- Bulbous nose\n- Epistaxis\n- Astigmatism\n- Deeply set eye\n- Atypical behavior\n- Delayed speech and language development\n- Motor delay\n- Growth delay\n- Talipes equinovarus\n- Large forehead\n- Dysphagia\n- Constipation\n- Asthma\n- Cerebral cortical atrophy\n- Nail dysplasia\n- EEG with polyspike wave complexes\n- Hypsarrhythmia\n- Highly arched eyebrow\n- Patellar hypoplasia\n- Prominent metopic ridge\n- Abnormality of the palpebral fissures\n- Axial hypotonia\n- Bilateral coxa valga\n- Intellectual disability, severe\n- Epileptic spasm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/08303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Thin vermilion border\n- Microcephaly\n- Abnormality of the philtrum\n- Full cheeks\n- Round face\n- Square face\n- Low-set ears\n- Bulbous nose\n- Wide nose\n- Webbed neck\n- Short neck\n- Astigmatism\n- Strabismus\n- Delayed speech and language development\n- Single transverse palmar crease\n- Motor delay\n- Plagiocephaly\n- Growth delay\n- Talipes equinovarus\n- Large forehead\n- Dysphagia\n- Nail dysplasia\n- Abnormal periventricular white matter morphology\n- Patellar aplasia\n- Abnormality of the palpebral fissures\n- Axial hypotonia\n- EEG with spike-wave complexes\n- Intellectual disability, severe\n- Clonic seizure\n- obsolete Small scrotum\n- Telangiectasia of the skin\n- Esophagitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/08304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Abnormal pinna morphology\n- Tapered finger\n- Poor suck\n- Hypocalcemia\n- T lymphocytopenia\n- Feeding difficulties in infancy\n- Fullness of paranasal tissue\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Velopharyngeal insufficiency\n- Macrotia\n- Pear-shaped nose\n- Global developmental delay\n- Ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Bulbous nose\n- Prominent nose\n- Narrow nose\n- Tapered finger\n- Global developmental delay\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Parietal bossing\n- Delayed eruption of primary teeth\n- Hypoplastic scapulae\n- Frontal bossing\n- Short stature\n- Abnormal facility in opposing the shoulders\n- Aplasia of the maxilla\n- Supernumerary tooth\n- Abnormality of the maxillary sinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Parietal bossing\n- Hypertelorism\n- Dental malocclusion\n- Frontal bossing\n- Failure of eruption of permanent teeth\n- Aplastic clavicle\n- Supernumerary tooth\n- Agenesis of mandibular incisor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Parietal bossing\n- Hypertelorism\n- Dental malocclusion\n- Frontal bossing\n- Failure of eruption of permanent teeth\n- Aplastic clavicle\n- Supernumerary tooth\n- Agenesis of mandibular incisor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thickened skin\n- Joint stiffness\n- Small for gestational age\n- Ascites\n- Pericardial effusion\n- Pleural effusion\n- Constrictive pericarditis\n- Proportionate short stature\n- Stiff skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/08311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/08312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Large fontanelles\n- Delayed eruption of teeth\n- Narrow chest\n- Abnormal clavicle morphology\n- Short stature\n- Wide cranial sutures\n- Supernumerary tooth\n- Prominent forehead\n- Aplastic zygomatic arch\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed cranial suture closure\n- Carious teeth\n- Delayed eruption of permanent teeth\n- Abnormal clavicle morphology\n- Frontal bossing\n- Multiple unerupted teeth\n- Short phalanx of finger\n- Midface retrusion\n- Irregular dentition\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Multiple unerupted teeth\n- Agenesis of premolar\n- Supernumerary tooth\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Dental malocclusion\n- Delayed eruption of permanent teeth\n- Rotated maxillary central incisors\n- Supernumerary tooth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Dental malocclusion\n- Delayed eruption of permanent teeth\n- Rotated maxillary central incisors\n- Supernumerary tooth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed cranial suture closure\n- Epicanthus\n- Hypertelorism\n- Delayed eruption of teeth\n- Premature birth\n- Frontal bossing\n- Persistent open anterior fontanelle\n- Depressed nasal bridge\n- Tooth agenesis\n- Short distal phalanx of finger\n- Abnormal frontal bone morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Parietal bossing\n- Mandibular prognathia\n- Multiple impacted teeth\n- Frontal bossing\n- Osteoarthritis\n- Mild short stature\n- Deviated nasal septum\n- Depressed nasal bridge\n- Delayed pneumatization of the mastoid process\n- Failure of eruption of permanent teeth\n- Glenoid fossa hypoplasia\n- Tooth agenesis\n- Abnormal temporal bone morphology\n- Supernumerary tooth\n- Fused teeth\n- Increased size of nasopharyngeal adenoids\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Parietal bossing\n- Mandibular prognathia\n- Multiple impacted teeth\n- Frontal bossing\n- Osteoarthritis\n- Mild short stature\n- Deviated nasal septum\n- Depressed nasal bridge\n- Delayed pneumatization of the mastoid process\n- Failure of eruption of permanent teeth\n- Glenoid fossa hypoplasia\n- Tooth agenesis\n- Abnormal temporal bone morphology\n- Supernumerary tooth\n- Fused teeth\n- Increased size of nasopharyngeal adenoids\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Hypertelorism\n- Carious teeth\n- Dental crowding\n- Delayed eruption of permanent teeth\n- Short clavicles\n- Brachydactyly\n- Tapered finger\n- Frontal bossing\n- Wormian bones\n- Rickets\n- Hypoplastic iliac wing\n- Wide pubic symphysis\n- Short stature\n- Depressed nasal bridge\n- Short thumb\n- Short phalanx of finger\n- Wide cranial sutures\n- Double tooth\n- Broad thumb\n- Midface retrusion\n- Fractured right clavicle\n- Abnormal sacroiliac joint morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Posteriorly rotated ears\n- Anteverted nares\n- Cataract\n- Synophrys\n- Eczema\n- Brachydactyly\n- Intellectual disability\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Constipation\n- Highly arched eyebrow\n- Obstructive sleep apnea\n- Severe short stature\n- Decreased body weight\n- Lumbar kyphoscoliosis\n- Hypoplasia of proximal radius\n- Hypoplasia of proximal fibula\n- Chronic lung disease\n- Thickened ears\n- Grade I vesicoureteral reflux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/08322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Posteriorly rotated ears\n- Anteverted nares\n- Cataract\n- Synophrys\n- Eczema\n- Brachydactyly\n- Intellectual disability\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Constipation\n- Highly arched eyebrow\n- Obstructive sleep apnea\n- Severe short stature\n- Decreased body weight\n- Lumbar kyphoscoliosis\n- Hypoplasia of proximal radius\n- Hypoplasia of proximal fibula\n- Chronic lung disease\n- Thickened ears\n- Grade I vesicoureteral reflux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/08323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Macrotia\n- Broad nasal tip\n- Strabismus\n- Ptosis\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Craniosynostosis\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Cavum septum pellucidum\n- Downturned corners of mouth\n- Sagittal craniosynostosis\n- Tented upper lip vermilion\n- Metopic synostosis\n- Feeding difficulties\n- EEG with generalized spikes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/08325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Preauricular skin tag\n- Macrotia\n- Broad nasal tip\n- Strabismus\n- Ptosis\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Craniosynostosis\n- Atrial septal defect\n- Patent ductus arteriosus\n- Downturned corners of mouth\n- Periventricular leukomalacia\n- Tented upper lip vermilion\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/08326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/08340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/08342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/08343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/08344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High palate\n- Cupped ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/08345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/08372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Laryngomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Laryngomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Laryngomalacia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glossoptosis\n- Cleft palate\n- Long philtrum\n- Micrognathia\n- Pectus excavatum\n- Brachydactyly\n- Patent foramen ovale\n- Sandal gap\n- Gastroesophageal reflux\n- Short stature\n- Decreased body weight\n- Deep palmar crease\n- Short 5th finger\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/08393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft soft palate\n- Facial hemangioma\n- Long philtrum\n- Micrognathia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Hypotonia\n- Hyporeflexia\n- Hip dysplasia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Lacrimal duct stenosis\n- Feeding difficulties\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/08394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Low-set ears\n- Global developmental delay\n- Overgrowth\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Low-set ears\n- Global developmental delay\n- Overgrowth\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Downturned corners of mouth\n- Short nose\n- Depressed nasal bridge\n- Almond-shaped palpebral fissure\n- Class III obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/08397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Triangular face\n- High forehead\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/08403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad philtrum\n- Downslanted palpebral fissures\n- Delayed closure of the anterior fontanelle\n- Excessive wrinkled skin\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/08410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad philtrum\n- Downslanted palpebral fissures\n- Delayed closure of the anterior fontanelle\n- Excessive wrinkled skin\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/08411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad philtrum\n- Downslanted palpebral fissures\n- Delayed closure of the anterior fontanelle\n- Excessive wrinkled skin\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/08412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Epicanthus\n- Low-set ears\n- Broad nasal tip\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/08415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/08416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Epicanthus\n- Broad forehead\n- Long philtrum\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Pointed chin\n- High forehead\n- Wide nasal bridge\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Narrow face\n- Pointed chin\n- Low-set, posteriorly rotated ears\n- Protruding ear\n- Open bite\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Coarse facial features\n- Pointed chin\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Pointed chin\n- Broad forehead\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Short philtrum\n- Wide nasal bridge\n- Postaxial foot polydactyly\n- Delayed gross motor development\n- Bilateral postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/08422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Short philtrum\n- Wide nasal bridge\n- Postaxial foot polydactyly\n- Delayed gross motor development\n- Bilateral postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/08423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Downslanted palpebral fissures\n- Abnormal pulmonary valve morphology\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Downslanted palpebral fissures\n- Abnormal pulmonary valve morphology\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Pointed chin\n- Overgrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Overgrowth\n- Nephroblastoma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/08427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Narrow face\n- Pointed chin\n- Protruding ear\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Narrow face\n- Epicanthus\n- Wide nasal bridge\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Epicanthus\n- Broad forehead\n- High forehead\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Coarse facial features\n- Epicanthus\n- Wide nasal bridge\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Pointed chin\n- Broad forehead\n- Long philtrum\n- High forehead\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Coarse facial features\n- Broad forehead\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Narrow face\n- Protruding ear\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Narrow face\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Narrow face\n- Epicanthus\n- Broad forehead\n- Long philtrum\n- Strabismus\n- Blepharophimosis\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Narrow face\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Epicanthus\n- Long philtrum\n- Strabismus\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Narrow face\n- Epicanthus\n- Pointed chin\n- Broad forehead\n- Long philtrum\n- Wide nasal bridge\n- Short nose\n- Elfin facies\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Narrow face\n- Coarse facial features\n- Pointed chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/08440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Triangular face\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Webbed neck\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Downslanted palpebral fissures\n- Ptosis\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Posteriorly rotated ears\n- Webbed neck\n- Downslanted palpebral fissures\n- Pectus excavatum\n- Fine hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Webbed neck\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Triangular face\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Webbed neck\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Proptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Triangular face\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Proptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Webbed neck\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Ptosis\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Triangular face\n- Thickened helices\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/08469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/08470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/08471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Protruding tongue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/08472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/08473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Macrotia\n- Protruding ear\n- Strabismus\n- Ptosis\n- Short columella\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrotia\n- Protruding ear\n- Ptosis\n- Long eyelashes\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Strabismus\n- Long eyelashes\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long eyelashes\n- Short columella\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Long eyelashes\n- Short columella\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long eyelashes\n- Widely spaced teeth\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Strabismus\n- Long eyelashes\n- Short columella\n- Highly arched eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Short lingual frenulum\n- Microcephaly\n- Macrotia\n- Protruding ear\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Protruding ear\n- Long eyelashes\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Protruding ear\n- Strabismus\n- Long eyelashes\n- Short columella\n- Highly arched eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Strabismus\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Protruding ear\n- Long eyelashes\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Long eyelashes\n- Widely spaced teeth\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ptosis\n- Short columella\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ptosis\n- Long eyelashes\n- Short columella\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long eyelashes\n- Short columella\n- Sparse lateral eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Long eyelashes\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Protruding ear\n- Long eyelashes\n- Short columella\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Bulbous nose\n- Telecanthus\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long face\n- Epicanthus\n- Bulbous nose\n- Wide nasal bridge\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Small earlobe\n- Bulbous nose\n- Prominent nasal bridge\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Small earlobe\n- Prominent nasal bridge\n- Abnormal eyelid morphology\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bulbous nose\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Small earlobe\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Epicanthus\n- Small earlobe\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Overfolded helix\n- Bulbous nose\n- Abnormal eyelid morphology\n- Telecanthus\n- Ptosis\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Epicanthus\n- Wide nasal bridge\n- Telecanthus\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Bulbous nose\n- Prominent nasal bridge\n- Abnormal facial shape\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Prominent nasal bridge\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long face\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n- Telecanthus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Small earlobe\n- Overfolded helix\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Bulbous nose\n- Telecanthus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Bulbous nose\n- Prominent nasal bridge\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long face\n- Bulbous nose\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/08516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Hypertelorism\n- Abnormal earlobe morphology\n- Long palpebral fissure\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Micrognathia\n- Abnormal earlobe morphology\n- Long palpebral fissure\n- Sparse lateral eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Epicanthus\n- Micrognathia\n- Abnormality of the outer ear\n- Strabismus\n- Ptosis\n- Long palpebral fissure\n- Short columella\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Abnormality of the outer ear\n- Anteverted nares\n- Webbed neck\n- Strabismus\n- Ptosis\n- Long palpebral fissure\n- Agenesis of maxillary lateral incisor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Micrognathia\n- High forehead\n- Abnormality of the outer ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Short columella\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Long palpebral fissure\n- Abnormal optic disc morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High palate\n- Thin upper lip vermilion\n- Protruding ear\n- Long eyelashes\n- Blue sclerae\n- Hypodontia\n- Widely spaced teeth\n- Prominent median palatal raphe\n- Clinodactyly of the 5th finger\n- Sparse lateral eyebrow\n- Enamel hypoplasia\n- Solitary median maxillary central incisor\n- Prominent digit pad\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Long face\n- Low anterior hairline\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Bulbous nose\n- Anteverted nares\n- Short neck\n- Downslanted palpebral fissures\n- Telecanthus\n- Short columella\n- Coarse hair\n- Sparse hair\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/08526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Facial asymmetry\n- Thick eyebrow\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Long palpebral fissure\n- Macrodontia\n- Tented upper lip vermilion\n- Prominent forehead\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low anterior hairline\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Low-set ears\n- Long eyelashes\n- Microdontia\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow face\n- Low anterior hairline\n- Macrotia\n- Coarse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Synophrys\n- Downturned corners of mouth\n- Attached earlobe\n- Darwin tubercle of helix\n- Exophoria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Anteverted nares\n- Ptosis\n- Hypermetropia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Epicanthus\n- Hypertelorism\n- Protruding ear\n- Broad nasal tip\n- Papilledema\n- Short nose\n- Almond-shaped palpebral fissure\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Long philtrum\n- Anteverted nares\n- Cutis marmorata\n- Hypopigmentation of the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/08535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Low-set, posteriorly rotated ears\n- Hypopigmentation of the skin\n- Frontal bossing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/08536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Depressed nasal tip\n- Long eyelashes\n- Highly arched eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High palate\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Protruding ear\n- Wide nasal bridge\n- Long palpebral fissure\n- Highly arched eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Epicanthus inversus\n- Microphthalmia\n- Iris coloboma\n- Long palpebral fissure\n- Acanthosis nigricans\n- Iris atrophy\n- Short columella\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Triangular face\n- Abnormality of prenatal development or birth\n- Severe failure to thrive\n- Frontal bossing\n- Relative macrocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/08541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/08542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/08543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cataract\n- Abnormality of refraction\n- Hemangioma\n- Motor delay\n- Umbilical hernia\n- Premature birth\n- Atrial septal defect\n- Abnormal mitral valve morphology\n- Pulmonic stenosis\n- Chylothorax\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cataract\n- Abnormality of refraction\n- Hemangioma\n- Motor delay\n- Umbilical hernia\n- Premature birth\n- Atrial septal defect\n- Abnormal mitral valve morphology\n- Pulmonic stenosis\n- Chylothorax\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glossoptosis\n- Short neck\n- Lymphedema\n- Polyhydramnios\n- Premature birth\n- Abnormal heart morphology\n- Ventricular septal defect\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Hydrops fetalis\n- Curly hair\n- Short stature\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short neck\n- Ptosis\n- Abnormal thorax morphology\n- Polyhydramnios\n- Premature birth\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Fetal ascites\n- Short stature\n- Chylothorax\n- Feeding difficulties\n- Fetal pleural effusion\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short neck\n- Ptosis\n- Lymphedema\n- Ventricular septal defect\n- Atrial septal defect\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Short stature\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Polyhydramnios\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short neck\n- Ptosis\n- Abnormal thorax morphology\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short neck\n- Ptosis\n- Abnormal thorax morphology\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short neck\n- Hemangioma\n- Polyhydramnios\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short neck\n- Hemangioma\n- Polyhydramnios\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydrocephalus\n- Ptosis\n- Abnormal thorax morphology\n- Intellectual disability\n- Motor delay\n- Polyhydramnios\n- Premature birth\n- Abnormal heart morphology\n- Ventricular septal defect\n- Atrial septal defect\n- Pulmonic stenosis\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydronephrosis\n- Strabismus\n- Ptosis\n- Abnormal thorax morphology\n- Bruising susceptibility\n- Lymphedema\n- Numerous nevi\n- Motor delay\n- Polyhydramnios\n- Premature birth\n- Abnormal heart morphology\n- Abnormal mitral valve morphology\n- Hypertrophic cardiomyopathy\n- Feeding difficulties\n- Fetal pleural effusion\n- Fetal chylothorax\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Short neck\n- Ptosis\n- Abnormality of refraction\n- Abnormal thorax morphology\n- Lymphedema\n- Seizure\n- Motor delay\n- Atrial septal defect\n- Abnormal mitral valve morphology\n- Hypertrophic cardiomyopathy\n- Hydrops fetalis\n- Short stature\n- Feeding difficulties\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short neck\n- Ptosis\n- Abnormality of refraction\n- Abnormal thorax morphology\n- Bruising susceptibility\n- Intellectual disability\n- Premature birth\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Short neck\n- Abnormality of refraction\n- Hemangioma\n- Intellectual disability\n- Motor delay\n- Polyhydramnios\n- Premature birth\n- Atrial septal defect\n- Intestinal lymphangiectasia\n- Short stature\n- Feeding difficulties\n- Submucous cleft of soft and hard palate\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydronephrosis\n- Strabismus\n- Abnormality of refraction\n- Bruising susceptibility\n- Hemangioma\n- Premature birth\n- Hypertrophic cardiomyopathy\n- Feeding difficulties\n- Keratosis pilaris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Ptosis\n- Abnormality of refraction\n- Pulmonic stenosis\n- Curly hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Short neck\n- Strabismus\n- Ptosis\n- Abnormality of refraction\n- Abnormal thorax morphology\n- Bruising susceptibility\n- Lymphedema\n- Hemangioma\n- Intellectual disability\n- Abnormal mitral valve morphology\n- Scoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypothyroidism\n- Bruising susceptibility\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short neck\n- Strabismus\n- Ptosis\n- Premature birth\n- Short stature\n- Feeding difficulties\n- Lipoma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Ptosis\n- Abnormality of refraction\n- Depression\n- Premature birth\n- Ventricular septal defect\n- Atrial septal defect\n- Curly hair\n- Scoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Pulmonic stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Low-set ears\n- Protruding ear\n- Short neck\n- Dental malocclusion\n- Pectus excavatum\n- Lymphedema\n- Failure to thrive in infancy\n- Low posterior hairline\n- Woolly hair\n- Varicose veins\n- Deep palmar crease\n- Moderately short stature\n- Unilateral cryptorchidism\n- Clubbing of fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Blue irides\n- Heterochromia iridis\n- Intellectual disability\n- Global developmental delay\n- White forelock\n- Silver-gray hair\n- Low hanging columella\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Blue irides\n- Heterochromia iridis\n- Intellectual disability\n- Global developmental delay\n- White forelock\n- Silver-gray hair\n- Low hanging columella\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Blue irides\n- Heterochromia iridis\n- Intellectual disability\n- Global developmental delay\n- White forelock\n- Silver-gray hair\n- Low hanging columella\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Blue irides\n- Heterochromia iridis\n- Intellectual disability\n- Global developmental delay\n- White forelock\n- Silver-gray hair\n- Low hanging columella\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Blue irides\n- Heterochromia iridis\n- Intellectual disability\n- Global developmental delay\n- White forelock\n- Silver-gray hair\n- Low hanging columella\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Underdeveloped nasal alae\n- Blue irides\n- Heterochromia iridis\n- Intellectual disability\n- Global developmental delay\n- White forelock\n- Silver-gray hair\n- Low hanging columella\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydrocele testis\n- Low-set ears\n- Atrial septal defect\n- Pleural effusion\n- Unilateral ptosis\n- Combined pre- and post-capillary pulmonary hypertension\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Telecanthus\n- Blue irides\n- White forelock\n- Lamellar cataract\n- Ectopic lacrimal punctum\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Blue irides\n- White forelock\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Blue irides\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Blue irides\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Hypertelorism\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Short nose\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Hypertelorism\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Short nose\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Retrognathia\n- Hypertelorism\n- Downslanted palpebral fissures\n- Telecanthus\n- Ptosis\n- Short nose\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Epicanthus\n- Long philtrum\n- Hypotonia\n- Global developmental delay\n- Congestive heart failure\n- Recurrent infections\n- Decreased circulating IgG level\n- Atrioventricular canal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/08583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Decreased body weight\n- Widely patent sagittal suture\n- Abnormality of the metopic suture\n- Microtia\n- Bicoronal synostosis\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/08584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Abnormal heart morphology\n- Abnormality of brain morphology\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/08585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Abnormal heart morphology\n- Wide intermamillary distance\n- Abnormality of brain morphology\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/08586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Abnormal heart morphology\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/08587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Long philtrum\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Synophrys\n- Micromelia\n- Curly eyelashes\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Downturned corners of mouth\n- Curly eyelashes\n- Proximal placement of thumb\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Downturned corners of mouth\n- Curly eyelashes\n- Proximal placement of thumb\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Brachycephaly\n- Microcephaly\n- Anteverted nares\n- Short neck\n- Long eyelashes\n- Abnormal eyebrow morphology\n- Downturned corners of mouth\n- Curly eyelashes\n- Proximal placement of thumb\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Absent speech\n- Small nail\n- Constipation\n- Aganglionic megacolon\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Clinodactyly of the 5th finger\n- Short distal phalanx of finger\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Absent speech\n- Small nail\n- Constipation\n- Aganglionic megacolon\n- Downturned corners of mouth\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- Clinodactyly of the 5th finger\n- Short distal phalanx of finger\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micrognathia\n- Pectus excavatum\n- Abnormality of the larynx\n- Abnormal foot morphology\n- Abnormality of tibia morphology\n- Short finger\n- Short thumb\n- Abnormal radial ray morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/08595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Large fontanelles\n- Retrognathia\n- Hypertelorism\n- Short chin\n- Long philtrum\n- High forehead\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Proptosis\n- Blue sclerae\n- Long palpebral fissure\n- Brachydactyly\n- Small for gestational age\n- Patent ductus arteriosus\n- Frontal bossing\n- Hypoplasia of the radius\n- Hypoplasia of the ulna\n- Short long bone\n- Mesomelia\n- Short nose\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Deep palmar crease\n- Wide intermamillary distance\n- Nail dystrophy\n- Upper limb undergrowth\n- Broad hallux\n- Short uvula\n- Midface retrusion\n- Clinodactyly of the 2nd finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/08596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Pointed chin\n- Prominent supraorbital ridges\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Chronic otitis media\n- Protruding ear\n- Strabismus\n- Downslanted palpebral fissures\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Generalized hypotonia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Delayed gross motor development\n- Abnormal sacral segmentation\n- Prominent protruding coccyx\n- Postnatal growth retardation\n- Oral-pharyngeal dysphagia\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/08597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Anteverted nares\n- Abnormal repetitive mannerisms\n- Impaired social interactions\n- Pectus excavatum\n- Hypotonia\n- Global developmental delay\n- Broad-based gait\n- Mild short stature\n- Prominent nasolabial fold\n- Prominent nasal tip\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Abnormality of upper lip vermillion\n- Pineal cyst\n- Arachnoid cyst\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/08598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Thin upper lip vermilion\n- Full cheeks\n- Square face\n- Hearing impairment\n- Absent earlobe\n- Narrow nasal bridge\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Sacral dimple\n- Motor delay\n- Joint hypermobility\n- Selective tooth agenesis\n- Overlapping toe\n- Sandal gap\n- Deep philtrum\n- Intellectual disability, moderate\n- Sleep disturbance\n- Highly arched eyebrow\n- Duodenal ulcer\n- Delayed skeletal maturation\n- Recurrent upper respiratory tract infections\n- Decreased circulating antibody level\n- Depressed nasal bridge\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Prominent forehead\n- Broad thumb\n- Feeding difficulties\n- Flat face\n- Short palpebral fissure\n- Fibular deviation of toes\n- Long fingers\n- Short ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/08599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Large earlobe\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/08601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Nystagmus\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Specific learning disability\n- Cerebral hypomyelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/08602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Macroglossia\n- Narrow palate\n- Bifid uvula\n- High palate\n- Dolichocephaly\n- Long face\n- Hearing impairment\n- Underdeveloped nasal alae\n- Downslanted palpebral fissures\n- Ptosis\n- Proptosis\n- Long palpebral fissure\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Ventricular septal defect\n- Pes planus\n- Abnormal hallux morphology\n- Constipation\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Vertebral segmentation defect\n- Short stature\n- Decreased body weight\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Prominent metopic ridge\n- Wide intermamillary distance\n- Impaired pain sensation\n- Broad lateral eyebrow\n- Pes valgus\n- Six lumbar vertebrae\n- Hypoplastic helices\n- Open bite\n- Agenesis of molar\n- Wide nasal ridge\n- Abnormality of the plantar skin of foot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Thin upper lip vermilion\n- Smooth philtrum\n- Short chin\n- Long philtrum\n- Low-set ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Deeply set eye\n- Ptosis\n- Upslanted palpebral fissure\n- Atypical behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Generalized hypotonia\n- Absent speech\n- Ventricular septal defect\n- Atrial septal defect\n- Respiratory distress\n- Delayed gross motor development\n- Exaggerated cupid's bow\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Cortical dysplasia\n- Elevated circulating alkaline phosphatase concentration\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Large earlobe\n- Narrow palpebral fissure\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Low-set ears\n- Wide nasal bridge\n- Deeply set eye\n- Decreased response to growth hormone stimulation test\n- Adducted thumb\n- Prominent metopic ridge\n- Overlapping fingers\n- Chin with horizontal crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/08605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/08606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Broad forehead\n- Hearing impairment\n- Macrotia\n- Deeply set eye\n- Downslanted palpebral fissures\n- Ptosis\n- Anxiety\n- Insulin-resistant diabetes mellitus\n- Intellectual disability\n- Hypotonia\n- Hip dysplasia\n- Thin nail\n- Truncal obesity\n- Sparse body hair\n- Cerebral calcification\n- Multiple joint contractures\n- Distal amyotrophy\n- Reduced bone mineral density\n- Calcification of the auricular cartilage\n- Elevated circulating alpha-fetoprotein concentration\n- Bone cyst\n- Overweight\n- Increased size of the mandible\n- Tics\n- Self-injurious behavior\n- Torus palatinus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/08607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Broad philtrum\n- Hypertelorism\n- Low-set ears\n- Macrotia\n- Bulbous nose\n- Downslanted palpebral fissures\n- Hypotonia\n- Failure to thrive\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Decreased circulating IgG level\n- Moderate global developmental delay\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/08608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Prominent fingertip pads\n- Seizure\n- Joint hypermobility\n- Failure to thrive\n- Intrauterine growth retardation\n- Sandal gap\n- Decreased body weight\n- Accelerated skeletal maturation\n- Sparse hair\n- Thick nasal alae\n- Short metacarpal\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Widely spaced teeth\n- Eczema\n- Atopic dermatitis\n- Prominent fingertip pads\n- Absent speech\n- Intrauterine growth retardation\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Sparse hair\n- Thick nasal alae\n- Hyperacusis\n- Prominent eyelashes\n- Moderate global developmental delay\n- Feeding difficulties\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Broad philtrum\n- Low anterior hairline\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Synophrys\n- Widely spaced teeth\n- Short attention span\n- Hypertrichosis\n- Seizure\n- Absent speech\n- Intrauterine growth retardation\n- Umbilical hernia\n- Short toe\n- Severe short stature\n- Decreased body weight\n- Deep palmar crease\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Prominent eyelashes\n- Broad thumb\n- Moderate global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Periorbital wrinkles\n- Prominent fingertip pads\n- Seizure\n- Sandal gap\n- Prominent interphalangeal joints\n- Sparse hair\n- Thick nasal alae\n- Cone-shaped epiphysis\n- Severe global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Delayed eruption of teeth\n- Widely spaced teeth\n- Prominent fingertip pads\n- Absent speech\n- Failure to thrive\n- Mitral regurgitation\n- Patent foramen ovale\n- Sandal gap\n- Facial hypertrichosis\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Ventricular septal hypertrophy\n- Sparse hair\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Periorbital wrinkles\n- Delayed eruption of teeth\n- Widely spaced teeth\n- Prominent fingertip pads\n- Absent speech\n- Failure to thrive\n- Mitral regurgitation\n- Patent foramen ovale\n- Sandal gap\n- Facial hypertrichosis\n- Delayed skeletal maturation\n- Short stature\n- Decreased body weight\n- Ventricular septal hypertrophy\n- Sparse hair\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Prominent eyelashes\n- Severe global developmental delay\n- Wide nasal base\n- Frequent temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Prominent fingertip pads\n- Seizure\n- Umbilical hernia\n- Scoliosis\n- Prominent interphalangeal joints\n- Sparse hair\n- Moderate global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Narrow nasal bridge\n- Downslanted palpebral fissures\n- Prominent fingertip pads\n- Seizure\n- Umbilical hernia\n- Scoliosis\n- Prominent interphalangeal joints\n- Sparse hair\n- Moderate global developmental delay\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/08617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Delayed cranial suture closure\n- Brachydactyly\n- Growth delay\n- Gastroesophageal reflux\n- Abnormal renal morphology\n- Wide nasal base\n- Clinodactyly\n- Hooded eyelid\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachydactyly\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Postnatal growth retardation\n- Clinodactyly\n- Abnormality of limbs\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachydactyly\n- Intrauterine growth retardation\n- Gastroesophageal reflux\n- Postnatal growth retardation\n- Clinodactyly\n- Abnormality of limbs\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Broad philtrum\n- Visual impairment\n- Optic disc pallor\n- Thick eyebrow\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hyperactivity\n- Pectus carinatum\n- Cutis marmorata\n- Global developmental delay\n- Bulbar palsy\n- Absent speech\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Dysphagia\n- Constipation\n- Gastroesophageal reflux\n- Apraxia\n- Delayed gross motor development\n- Sleep disturbance\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Abnormal femoral neck morphology\n- Short stature\n- Cranial hyperostosis\n- Lumbar kyphosis\n- Ankyloglossia\n- Delayed fine motor development\n- Intellectual disability, severe\n- Clinodactyly\n- Myopic astigmatism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genital system\n- Microcephaly\n- Hearing impairment\n- Atypical behavior\n- Seizure\n- Intellectual disability, moderate\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genital system\n- Microcephaly\n- Hearing impairment\n- Atypical behavior\n- Seizure\n- Intellectual disability, moderate\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long face\n- Prominent nasal bridge\n- Myopia\n- Thick eyebrow\n- Synophrys\n- Dental crowding\n- Hypothyroidism\n- Back pain\n- Short 5th finger\n- Hip pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydrocephalus\n- Hearing impairment\n- Myopia\n- Sacral dimple\n- Neonatal hypotonia\n- Pes planus\n- Poor motor coordination\n- Spina bifida\n- Scoliosis\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n- Mild global developmental delay\n- Tented philtrum\n- Keratosis pilaris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/08626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal pinna morphology\n- Bulbous nose\n- Long nose\n- Mandibulofacial dysostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/08627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Wide nose\n- Narrow nasal bridge\n- Deeply set eye\n- Long nose\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Brachydactyly\n- Intellectual disability, mild\n- Low hanging columella\n- Short 5th metacarpal\n- Broad fingertip\n- Broad thumb\n- Moderate expressive language delay\n- Clinodactyly\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Brachydactyly\n- Intellectual disability, mild\n- Low hanging columella\n- Short 5th metacarpal\n- Broad fingertip\n- Broad thumb\n- Moderate expressive language delay\n- Clinodactyly\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin vermilion border\n- Hearing impairment\n- Low-set, posteriorly rotated ears\n- Low-set ears\n- Protruding ear\n- Bulbous nose\n- Prominent nose\n- Hematuria\n- Hypertension\n- Brachydactyly\n- Meningitis\n- Growth delay\n- Expressive language delay\n- Clubbing of fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Multicystic kidney dysplasia\n- Hypoplastic labia minora\n- Microcephaly\n- Prominent nasal bridge\n- Optic atrophy\n- Abnormal rib morphology\n- Intellectual disability\n- Flexion contracture\n- Anteriorly placed anus\n- Atrial septal defect\n- Talipes equinovarus\n- Abnormal patella morphology\n- Aplasia\/Hypoplasia of the patella\n- Aplasia\/Hypoplasia of the corpus callosum\n- Neurodevelopmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/08632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Congenital diaphragmatic hernia\n- Global developmental delay\n- Patent ductus arteriosus\n- Hypoplastic fingernail\n- Bilateral camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/08633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/08634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad nasal tip\n- Long palpebral fissure\n- Global developmental delay\n- Hyperphosphatemia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Retinal dystrophy\n- Postaxial hand polydactyly\n- Global developmental delay\n- Obesity\n- Postaxial foot polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/08637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Postaxial hand polydactyly\n- Global developmental delay\n- Obesity\n- Postaxial foot polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/08638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Blue irides\n- White forelock\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Cleft soft palate\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Posteriorly rotated ears\n- Recurrent otitis media\n- Anteverted nares\n- Upslanted palpebral fissure\n- Intellectual disability\n- Global developmental delay\n- Brisk reflexes\n- Failure to thrive\n- Constipation\n- Bilateral tonic-clonic seizure\n- Recurrent aspiration pneumonia\n- Ventriculomegaly\n- Broad-based gait\n- Limb hypertonia\n- Inverted nipples\n- Prominent nasal tip\n- Sparse lateral eyebrow\n- Limited hip movement\n- Feeding difficulties in infancy\n- Limitation of knee mobility\n- Thick vermilion border\n- Arachnoid cyst\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/08640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Anteverted nares\n- Upslanted palpebral fissure\n- Diastema\n- Delayed speech and language development\n- Seizure\n- Motor delay\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/08641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Convex nasal ridge\n- obsolete Decreased subcutaneous fat\n- Prominent superficial veins\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Umbilical hernia\n- Oligohydramnios\n- Patent ductus arteriosus\n- Small nail\n- Decreased skull ossification\n- Hypoplasia of the abdominal wall musculature\n- Excessive wrinkled skin\n- Prematurely aged appearance\n- Short distal phalanx of finger\n- Abnormality of the scalp hair\n- Sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/08642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Large fontanelles\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Convex nasal ridge\n- obsolete Decreased subcutaneous fat\n- Prominent superficial veins\n- Intrauterine growth retardation\n- Small for gestational age\n- Oligohydramnios\n- Small nail\n- Neonatal respiratory distress\n- Abnormal enchondral ossification\n- Excessive wrinkled skin\n- Prematurely aged appearance\n- Short distal phalanx of finger\n- Abnormality of the scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/08643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypotonia\n- Dandy-Walker malformation\n- Psychomotor deterioration\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/08644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/08657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Global developmental delay\n- Axial hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/08658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/08674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/08675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Gait ataxia\n- Sleep disturbance\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Gait ataxia\n- Sleep disturbance\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Gait disturbance\n- Joint hypermobility\n- Delayed gross motor development\n- Sleep disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Gait ataxia\n- Cerebral cortical atrophy\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Gait ataxia\n- Cerebral cortical atrophy\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Joint hypermobility\n- Gait ataxia\n- Cerebral cortical atrophy\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autism\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait disturbance\n- Joint hypermobility\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait disturbance\n- Sleep disturbance\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait disturbance\n- Sleep disturbance\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Autism\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait disturbance\n- Joint hypermobility\n- Sleep disturbance\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait disturbance\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Autism\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait ataxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Strabismus\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Cerebellar atrophy\n- Gait ataxia\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/08689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/08690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/08691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/08693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/08694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/08695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/08697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Widow's peak\n- Calvarial skull defect\n- Patent ductus arteriosus\n- Decreased skull ossification\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/08698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Downslanted palpebral fissures\n- Primary amenorrhea\n- Intellectual disability\n- Overgrowth\n- Patent ductus arteriosus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/08700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/08701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/08702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/08703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/08704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/08705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/08706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/08707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Hypertrophic cardiomyopathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Hypertrophic cardiomyopathy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/08709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroorchidism\n- Macroglossia\n- Gingival overgrowth\n- Coarse facial features\n- Bulbous nose\n- Prominent nose\n- Bifid nasal tip\n- Synophrys\n- Hypotonia\n- Global developmental delay\n- Encephalopathy\n- Anonychia\n- Kyphosis\n- Hyperlordosis\n- Pes valgus\n- Aplasia of the distal phalanges of the hand\n- Unilateral deafness\n- Aplasia of the distal phalanges of the toes\n- Intellectual disability, severe\n- Thick vermilion border\n- Thick hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/08710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Coarse facial features\n- Dysostosis multiplex\n- Intellectual disability\n- Progressive neurologic deterioration\n- Multiple joint contractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Sudden cardiac death\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Hearing impairment\n- Cupped ear\n- Macrotia\n- Protruding ear\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Bruising susceptibility\n- Brachydactyly\n- Prominent fingertip pads\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Abnormal heart morphology\n- Ventricular septal defect\n- Headache\n- Arthralgia\n- Decreased circulating total IgM\n- Decreased circulating IgG level\n- Short stature\n- Prematurely aged appearance\n- Bleeding with minor or no trauma\n- Feeding difficulties\n- Endometriosis\n- Insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Hearing impairment\n- Cupped ear\n- Macrotia\n- Protruding ear\n- Myopia\n- Long palpebral fissure\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Bruising susceptibility\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Portal hypertension\n- Decreased liver function\n- Ascites\n- Aortic regurgitation\n- Autoimmune thrombocytopenia\n- Esophageal varix\n- Spinal cord compression\n- Highly arched eyebrow\n- Immunodeficiency\n- Aortic aneurysm\n- Abnormal pulmonary interstitial morphology\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Recurrent sinusitis\n- Broad eyebrow\n- Bleeding with minor or no trauma\n- Psoriasiform lesion\n- Adenocarcinoma of the colon\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Hearing impairment\n- Cupped ear\n- Macrotia\n- Protruding ear\n- Myopia\n- Long palpebral fissure\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Bruising susceptibility\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Portal hypertension\n- Decreased liver function\n- Ascites\n- Aortic regurgitation\n- Autoimmune thrombocytopenia\n- Esophageal varix\n- Spinal cord compression\n- Highly arched eyebrow\n- Immunodeficiency\n- Aortic aneurysm\n- Abnormal pulmonary interstitial morphology\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Recurrent sinusitis\n- Broad eyebrow\n- Bleeding with minor or no trauma\n- Psoriasiform lesion\n- Adenocarcinoma of the colon\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Hearing impairment\n- Cupped ear\n- Macrotia\n- Protruding ear\n- Myopia\n- Long palpebral fissure\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Bruising susceptibility\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Portal hypertension\n- Decreased liver function\n- Ascites\n- Aortic regurgitation\n- Autoimmune thrombocytopenia\n- Esophageal varix\n- Spinal cord compression\n- Highly arched eyebrow\n- Immunodeficiency\n- Aortic aneurysm\n- Abnormal pulmonary interstitial morphology\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Recurrent sinusitis\n- Broad eyebrow\n- Bleeding with minor or no trauma\n- Psoriasiform lesion\n- Adenocarcinoma of the colon\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Hearing impairment\n- Cupped ear\n- Macrotia\n- Protruding ear\n- Myopia\n- Long palpebral fissure\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Bruising susceptibility\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Portal hypertension\n- Decreased liver function\n- Ascites\n- Aortic regurgitation\n- Autoimmune thrombocytopenia\n- Esophageal varix\n- Spinal cord compression\n- Highly arched eyebrow\n- Immunodeficiency\n- Aortic aneurysm\n- Abnormal pulmonary interstitial morphology\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Recurrent sinusitis\n- Broad eyebrow\n- Bleeding with minor or no trauma\n- Psoriasiform lesion\n- Adenocarcinoma of the colon\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Hearing impairment\n- Cupped ear\n- Macrotia\n- Protruding ear\n- Myopia\n- Long palpebral fissure\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Bruising susceptibility\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Portal hypertension\n- Decreased liver function\n- Ascites\n- Aortic regurgitation\n- Autoimmune thrombocytopenia\n- Esophageal varix\n- Spinal cord compression\n- Highly arched eyebrow\n- Immunodeficiency\n- Aortic aneurysm\n- Abnormal pulmonary interstitial morphology\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Recurrent sinusitis\n- Broad eyebrow\n- Bleeding with minor or no trauma\n- Psoriasiform lesion\n- Adenocarcinoma of the colon\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hearing impairment\n- Myopia\n- Long palpebral fissure\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hip dysplasia\n- Highly arched eyebrow\n- Decreased circulating IgA level\n- Short stature\n- Sparse lateral eyebrow\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Broad eyebrow\n- Feeding difficulties\n- Impaired binding of factor VIII to VWF\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hearing impairment\n- Myopia\n- Long palpebral fissure\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hip dysplasia\n- Highly arched eyebrow\n- Decreased circulating IgA level\n- Short stature\n- Sparse lateral eyebrow\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Broad eyebrow\n- Feeding difficulties\n- Impaired binding of factor VIII to VWF\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hearing impairment\n- Myopia\n- Long palpebral fissure\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hip dysplasia\n- Highly arched eyebrow\n- Decreased circulating IgA level\n- Short stature\n- Sparse lateral eyebrow\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Broad eyebrow\n- Feeding difficulties\n- Impaired binding of factor VIII to VWF\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hearing impairment\n- Myopia\n- Long palpebral fissure\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hip dysplasia\n- Highly arched eyebrow\n- Decreased circulating IgA level\n- Short stature\n- Sparse lateral eyebrow\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Broad eyebrow\n- Feeding difficulties\n- Impaired binding of factor VIII to VWF\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hearing impairment\n- Myopia\n- Long palpebral fissure\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hip dysplasia\n- Highly arched eyebrow\n- Decreased circulating IgA level\n- Short stature\n- Sparse lateral eyebrow\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Broad eyebrow\n- Feeding difficulties\n- Impaired binding of factor VIII to VWF\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hearing impairment\n- Myopia\n- Long palpebral fissure\n- Depression\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hip dysplasia\n- Highly arched eyebrow\n- Decreased circulating IgA level\n- Short stature\n- Sparse lateral eyebrow\n- Prematurely aged appearance\n- Eversion of lateral third of lower eyelids\n- Broad eyebrow\n- Feeding difficulties\n- Impaired binding of factor VIII to VWF\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/08724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Joint contracture of the hand\n- Chin with H-shaped crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Pursed lips\n- Long philtrum\n- Deeply set eye\n- Irritability\n- Lethargy\n- Cardiomegaly\n- Right ventricular failure\n- Talipes equinovarus\n- Respiratory insufficiency\n- Dyspnea\n- Scoliosis\n- Multiple joint contractures\n- Prominent nasolabial fold\n- Recurrent pneumonia\n- Generalized edema\n- Abnormal skeletal morphology\n- Camptodactyly\n- Left ventricular systolic dysfunction\n- Right atrial enlargement\n- Right axis deviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Mask-like facies\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Wide nasal bridge\n- Strabismus\n- Talipes equinovarus\n- Rocker bottom foot\n- Depressed nasal bridge\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Narrow mouth\n- Thin vermilion border\n- Broad forehead\n- Whistling appearance\n- Low-set ears\n- Wide nose\n- Deeply set eye\n- Downslanted palpebral fissures\n- Deformed rib cage\n- Bilateral talipes equinovarus\n- Thoracic scoliosis\n- Prominent nasolabial fold\n- Ulnar deviation of finger\n- Contracture of thumb\n- Concave nasal ridge\n- Feeding difficulties\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Whistling appearance\n- Distal arthrogryposis\n- Ulnar deviation of finger\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Whistling appearance\n- Ulnar deviation of the hand or of fingers of the hand\n- Distal arthrogryposis\n- Ulnar deviation of finger\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Whistling appearance\n- Talipes equinovarus\n- Ulnar deviation of finger\n- Joint contracture of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Whistling appearance\n- Ulnar deviation of finger\n- Joint contracture of the hand\n- Chin with H-shaped crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Whistling appearance\n- Underdeveloped nasal alae\n- Interphalangeal joint contracture of finger\n- Dandy-Walker malformation\n- Intrauterine growth retardation\n- Metatarsus adductus\n- Ulnar deviation of the wrist\n- Distal arthrogryposis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Whistling appearance\n- Abnormal foot morphology\n- Talipes equinovarus\n- Joint contracture of the hand\n- Ulnar deviation of the hand\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Pursed lips\n- Ptosis\n- Talipes equinovarus\n- Foot joint contracture\n- Calf muscle hypoplasia\n- Hand muscle atrophy\n- Joint contracture of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Mask-like facies\n- Hypertelorism\n- Long philtrum\n- Whistling appearance\n- Posteriorly rotated ears\n- Abnormal pinna morphology\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Short neck\n- Deeply set eye\n- Microphthalmia\n- Cutis laxa\n- Adducted thumb\n- Polyhydramnios\n- Talipes equinovarus\n- Decreased hip abduction\n- Short nose\n- Short stature\n- Decreased body weight\n- Ulnar deviation of finger\n- Chin with H-shaped crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Overfolded helix\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Pursed lips\n- High palate\n- Mask-like facies\n- Hypermetropia\n- Pectus excavatum\n- Hitchhiker thumb\n- Bilateral ptosis\n- Respiratory distress\n- Genu recurvatum\n- Thoracolumbar scoliosis\n- Short stature\n- Limited knee flexion\n- Copper beaten skull\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Trismus\n- Epicanthus\n- Long philtrum\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Telecanthus\n- Ptosis\n- Abnormal finger morphology\n- Knee dislocation\n- Depressed nasal bridge\n- Abnormal nostril morphology\n- Dimple chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microglossia\n- Narrow palate\n- Low anterior hairline\n- Hypertelorism\n- Long philtrum\n- Whistling appearance\n- Micrognathia\n- Recurrent otitis media\n- Conductive hearing impairment\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Deeply set eye\n- Ptosis\n- Blepharophimosis\n- Nystagmus\n- Dental crowding\n- Depression\n- Cyanosis\n- Muscle weakness\n- Craniosynostosis\n- Failure to thrive\n- Slender build\n- Polyhydramnios\n- Hypernasal speech\n- Dysphagia\n- Malignant hyperthermia\n- Pneumonia\n- Apnea\n- Headache\n- Scoliosis\n- Abnormality of the knee\n- Short nose\n- Increased muscle fatiguability\n- Short stature\n- Poor appetite\n- Neck joint contracture\n- Postnatal growth retardation\n- Patellar subluxation\n- Recurrent sinusitis\n- Moderate global developmental delay\n- Flat face\n- Hyperpyrexia\n- Upper-limb joint contracture\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microglossia\n- Narrow palate\n- Low anterior hairline\n- Hypertelorism\n- Long philtrum\n- Whistling appearance\n- Micrognathia\n- Recurrent otitis media\n- Conductive hearing impairment\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Short neck\n- Strabismus\n- Deeply set eye\n- Ptosis\n- Blepharophimosis\n- Nystagmus\n- Dental crowding\n- Depression\n- Cyanosis\n- Muscle weakness\n- Craniosynostosis\n- Failure to thrive\n- Slender build\n- Polyhydramnios\n- Hypernasal speech\n- Dysphagia\n- Malignant hyperthermia\n- Pneumonia\n- Apnea\n- Headache\n- Scoliosis\n- Abnormality of the knee\n- Short nose\n- Increased muscle fatiguability\n- Short stature\n- Poor appetite\n- Neck joint contracture\n- Postnatal growth retardation\n- Patellar subluxation\n- Recurrent sinusitis\n- Moderate global developmental delay\n- Flat face\n- Hyperpyrexia\n- Upper-limb joint contracture\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Inguinal hernia\n- Narrow mouth\n- Microglossia\n- High palate\n- Everted lower lip vermilion\n- Mask-like facies\n- Long philtrum\n- Wide nasal bridge\n- Deeply set eye\n- Blepharophimosis\n- Overlapping toe\n- Polysyndactyly of hallux\n- Everted upper lip vermilion\n- Feeding difficulties\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, mild\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Retrognathia\n- Low-set ears\n- Abnormal pinna morphology\n- Prominent nose\n- Shield chest\n- Talipes equinovarus\n- Wide intermamillary distance\n- Everted upper lip vermilion\n- Chin with H-shaped crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Microglossia\n- High palate\n- Epicanthus\n- Mask-like facies\n- Long philtrum\n- Micrognathia\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Strabismus\n- Deeply set eye\n- Telecanthus\n- Blepharophimosis\n- Upper eyelid coloboma\n- Dental malocclusion\n- Short nose\n- Increased overbite\n- Overjet\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Microglossia\n- High palate\n- Epicanthus\n- Mask-like facies\n- Long philtrum\n- Micrognathia\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Strabismus\n- Deeply set eye\n- Telecanthus\n- Blepharophimosis\n- Upper eyelid coloboma\n- Dental malocclusion\n- Short nose\n- Increased overbite\n- Overjet\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Oxycephaly\n- Broad philtrum\n- Mandibular prognathia\n- Triangular face\n- Broad forehead\n- Low-set ears\n- Short neck\n- Broad neck\n- Astigmatism\n- Downslanted palpebral fissures\n- Hypermetropia\n- Thick eyebrow\n- Pectus carinatum\n- Small thenar eminence\n- Limitation of joint mobility\n- Barrel-shaped chest\n- Talipes equinovarus\n- Anonychia\n- Low posterior hairline\n- Clumsiness\n- Highly arched eyebrow\n- Scoliosis\n- Cubitus valgus\n- Short stature\n- Flat forehead\n- Prominent nasolabial fold\n- Congenital talipes calcaneovalgus\n- Limitation of neck motion\n- Shoulder muscle hypoplasia\n- Uplifted earlobe\n- Camptodactyly\n- Tip-toe gait\n- Clinodactyly\n- Telangiectasia of the skin\n- Blue nevus\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Narrow mouth\n- Microglossia\n- Pursed lips\n- Trismus\n- Mask-like facies\n- Hypertelorism\n- Micrognathia\n- Deeply set eye\n- Thick eyebrow\n- Short nose\n- Limited neck flexion\n- Ulnar deviation of finger\n- Camptodactyly\n- Limited neck extension\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Specific learning disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Short neck\n- Thick eyebrow\n- Narrow chest\n- Premature birth\n- Patent ductus arteriosus\n- Congenital hypertrophy of left ventricle\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/08753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/08754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/08755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/08756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Disproportionate tall stature\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/08757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/08758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Atypical behavior\n- Psychosis\n- Self-mutilation\n- Intellectual disability\n- Obesity\n- Abnormal aggressive, impulsive or violent behavior\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/08759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Epileptic spasm\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/08760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Abnormal facial shape\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/08761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Abnormal facial shape\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/08762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Abnormal facial shape\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/08763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/08764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Short neck\n- Microphthalmia\n- Hypotelorism\n- Delayed speech and language development\n- Motor delay\n- Talipes equinovarus\n- Rocker bottom foot\n- Arthrogryposis multiplex congenita\n- Feeding difficulties in infancy\n- Supernumerary tooth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/08765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Unilateral ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/08766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Strabismus\n- Delayed speech and language development\n- Hypotonia\n- Delayed gross motor development\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/08767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Joint hypermobility\n- Redundant skin\n- Scoliosis\n- Distal arthrogryposis\n- Hip subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/08769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Delayed speech and language development\n- Hyperactivity\n- Global developmental delay\n- Vomiting\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Delayed speech and language development\n- Hyperactivity\n- Global developmental delay\n- Vomiting\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Epicanthus\n- Delayed speech and language development\n- Hyperactivity\n- Global developmental delay\n- Vomiting\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/08772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Sensorineural hearing impairment\n- Brachydactyly\n- Global developmental delay\n- Hypoplastic fingernail\n- Dystrophic toenail\n- Nail dysplasia\n- Aganglionic megacolon\n- Exaggerated cupid's bow\n- Elevated circulating alkaline phosphatase concentration\n- Absent fifth fingernail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Seizure\n- Hypotonia\n- Hypoglycemia\n- Delayed gross motor development\n- Developmental regression\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/08775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Delayed gross motor development\n- Leukodystrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/08787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormal cochlea morphology\n- Astigmatism\n- Strabismus\n- Optic nerve hypoplasia\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Specific learning disability\n- Absent speech\n- Rectal prolapse\n- Ventriculomegaly\n- Cavum septum pellucidum\n- Intussusception\n- Hernia of the abdominal wall\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/08788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Strabismus\n- Hypermetropia\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Syncope\n- Specific learning disability\n- Absent speech\n- Abnormal cerebral white matter morphology\n- Focal-onset seizure\n- Gastrostomy tube feeding in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/08789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Astigmatism\n- Myopia\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Specific learning disability\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/08790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Sensorineural hearing impairment\n- Protruding ear\n- Proptosis\n- Intellectual disability\n- Global developmental delay\n- Kyphosis\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Sensorineural hearing impairment\n- Protruding ear\n- Proptosis\n- Intellectual disability\n- Global developmental delay\n- Kyphosis\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypopigmentation of the skin\n- Hypoplasia of the fovea\n- Chorioretinal hypopigmentation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/08793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Intellectual disability\n- Agenesis of corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/08795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/08796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypoplastic male external genitalia\n- Macroglossia\n- Thin upper lip vermilion\n- Microcephaly\n- Wide anterior fontanel\n- Dolichocephaly\n- Small face\n- Mandibular prognathia\n- Short philtrum\n- Triangular face\n- Broad forehead\n- Micrognathia\n- Low-set ears\n- Microphthalmia\n- Blue sclerae\n- Thin skin\n- Hypertrichosis\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Sparse scalp hair\n- Birth length less than 3rd percentile\n- Reduced subcutaneous adipose tissue\n- Decreased skull ossification\n- Coronal craniosynostosis\n- Ascending tubular aorta aneurysm\n- Progeroid facial appearance\n- Absent distal phalanges\n- Aplasia\/Hypoplasia of the nails\n- Microtia\n- Postnatal growth retardation\n- Abnormality of the hairline\n- Short distal phalanx of finger\n- Dermal translucency\n- Protruding tongue\n- Mild global developmental delay\n- Midface retrusion\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/08798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide anterior fontanel\n- Epicanthus\n- Micrognathia\n- Astigmatism\n- Telecanthus\n- Epicanthus inversus\n- Blepharophimosis\n- Blue sclerae\n- Photophobia\n- Dental crowding\n- Delayed speech and language development\n- Osteopenia\n- Prominent superficial veins\n- Wrist flexion contracture\n- Hypotonia\n- Motor delay\n- Small for gestational age\n- High pitched voice\n- Bilateral talipes equinovarus\n- Frontal bossing\n- Alopecia of scalp\n- Recurrent fractures\n- Short stature\n- Decreased body weight\n- Decreased skull ossification\n- Ankle flexion contracture\n- Sparse hair\n- Wide cranial sutures\n- Epiblepharon\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/08799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide anterior fontanel\n- Epicanthus\n- Micrognathia\n- Astigmatism\n- Telecanthus\n- Epicanthus inversus\n- Blepharophimosis\n- Blue sclerae\n- Photophobia\n- Dental crowding\n- Delayed speech and language development\n- Osteopenia\n- Prominent superficial veins\n- Wrist flexion contracture\n- Hypotonia\n- Motor delay\n- Small for gestational age\n- High pitched voice\n- Bilateral talipes equinovarus\n- Frontal bossing\n- Alopecia of scalp\n- Recurrent fractures\n- Short stature\n- Decreased body weight\n- Decreased skull ossification\n- Ankle flexion contracture\n- Sparse hair\n- Wide cranial sutures\n- Epiblepharon\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/08800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Micrognathia\n- Deeply set eye\n- Delayed speech and language development\n- Prominent scalp veins\n- Hypotonia\n- Motor delay\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Frontal bossing\n- Neonatal respiratory distress\n- Sparse hair\n- Postnatal growth retardation\n- Lipodystrophy\n- Dermal translucency\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Micrognathia\n- Deeply set eye\n- Delayed speech and language development\n- Prominent scalp veins\n- Hypotonia\n- Motor delay\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Frontal bossing\n- Neonatal respiratory distress\n- Sparse hair\n- Postnatal growth retardation\n- Lipodystrophy\n- Dermal translucency\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Micrognathia\n- Deeply set eye\n- Thin skin\n- Prominent scalp veins\n- Hypotonia\n- Motor delay\n- Agenesis of corpus callosum\n- Flexion contracture\n- Joint hypermobility\n- Intrauterine growth retardation\n- Sparse scalp hair\n- Lipodystrophy\n- Dermal translucency\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Micrognathia\n- Deeply set eye\n- Thin skin\n- Prominent scalp veins\n- Hypotonia\n- Motor delay\n- Agenesis of corpus callosum\n- Flexion contracture\n- Joint hypermobility\n- Intrauterine growth retardation\n- Sparse scalp hair\n- Lipodystrophy\n- Dermal translucency\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Micrognathia\n- Deeply set eye\n- Myopia\n- Thin skin\n- Prominent scalp veins\n- Hypotonia\n- Agenesis of corpus callosum\n- Joint hypermobility\n- Intrauterine growth retardation\n- Abnormal heart morphology\n- Sparse scalp hair\n- Neonatal respiratory distress\n- Lipodystrophy\n- Dermal translucency\n- Premature skin wrinkling\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Hypotelorism\n- Oligodontia\n- Delayed eruption of permanent teeth\n- Delayed speech and language development\n- Thin skin\n- Prominent scalp veins\n- Motor delay\n- Flexion contracture\n- Intrauterine growth retardation\n- Abnormal heart morphology\n- Frontal bossing\n- Sparse scalp hair\n- Neonatal respiratory distress\n- Short stature\n- Lipodystrophy\n- Dermal translucency\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Hypotelorism\n- Oligodontia\n- Delayed eruption of permanent teeth\n- Delayed speech and language development\n- Thin skin\n- Prominent scalp veins\n- Motor delay\n- Flexion contracture\n- Intrauterine growth retardation\n- Abnormal heart morphology\n- Frontal bossing\n- Sparse scalp hair\n- Neonatal respiratory distress\n- Short stature\n- Lipodystrophy\n- Dermal translucency\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Hypotelorism\n- Prominent scalp veins\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Abnormal heart morphology\n- Frontal bossing\n- Sparse scalp hair\n- Neonatal respiratory distress\n- Sparse hair\n- Lipodystrophy\n- Dermal translucency\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Triangular face\n- Micrognathia\n- Low-set ears\n- Hypotelorism\n- Prominent scalp veins\n- Agenesis of corpus callosum\n- Intrauterine growth retardation\n- Abnormal heart morphology\n- Frontal bossing\n- Sparse scalp hair\n- Neonatal respiratory distress\n- Sparse hair\n- Lipodystrophy\n- Dermal translucency\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/08809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tapered finger\n- Small foramen magnum\n- Abnormality of the odontoid process\n- Cervical C2\/C3 vertebral fusion\n- Cleft vertebral arch\n- Basilar invagination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/08818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inappropriate laughter\n- Intellectual disability\n- Sleep disturbance\n- Abnormal aggressive, impulsive or violent behavior\n- Stereotypical hand wringing\n- Abnormality of digestive system physiology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/08819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Posteriorly rotated ears\n- Pectus excavatum\n- Pulmonic stenosis\n- Mild short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Posteriorly rotated ears\n- Pectus excavatum\n- Pulmonic stenosis\n- Mild short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Narrow forehead\n- Long philtrum\n- High forehead\n- Posteriorly rotated ears\n- Anteverted nares\n- Short neck\n- Strabismus\n- Ptosis\n- Abnormal sternum morphology\n- Hyperpigmentation of the skin\n- Hyperkeratosis\n- Hypotonia\n- Joint hypermobility\n- Growth delay\n- Mitral valve prolapse\n- Pulmonic stenosis\n- Curly hair\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Large earlobe\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- High forehead\n- Low-set ears\n- Short neck\n- Astigmatism\n- Strabismus\n- Ptosis\n- Nystagmus\n- Sparse eyelashes\n- Cafe-au-lait spot\n- Hyperkeratosis\n- Growth delay\n- Polyhydramnios\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Ventriculomegaly\n- Curly hair\n- Intellectual disability, moderate\n- Short nose\n- Nevus\n- Depressed nasal bridge\n- Redundant neck skin\n- Sparse hair\n- Feeding difficulties in infancy\n- Thickened ears\n- Keratosis pilaris\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Narrow forehead\n- Long philtrum\n- High forehead\n- Posteriorly rotated ears\n- Low-set ears\n- Bulbous nose\n- Anteverted nares\n- Webbed neck\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Myopia\n- Sparse eyelashes\n- Carious teeth\n- Abnormal sternum morphology\n- Dry skin\n- Hyperkeratosis\n- Seizure\n- Hypertonia\n- Deep-set nails\n- Low posterior hairline\n- Curly hair\n- Short nose\n- Nevus\n- Short stature\n- Depressed nasal bridge\n- Joint hyperflexibility\n- Underdeveloped supraorbital ridges\n- Thickened ears\n- Intellectual disability, severe\n- Feeding difficulties\n- Keratosis pilaris\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Anteverted nares\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Sparse eyelashes\n- Cafe-au-lait spot\n- Hyperkeratosis\n- Hypotonia\n- Intellectual disability, mild\n- Joint hypermobility\n- Curly hair\n- Fine hair\n- Short nose\n- Nevus\n- Preauricular pit\n- Depressed nasal bridge\n- Redundant neck skin\n- Sparse hair\n- Underdeveloped supraorbital ridges\n- Thickened ears\n- Thick vermilion border\n- Keratosis pilaris\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/08825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Global developmental delay\n- Mental deterioration\n- Dysphagia\n- Constipation\n- Recurrent respiratory infections\n- Recurrent pneumonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/08826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Exotropia\n- Synophrys\n- Delayed speech and language development\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Exotropia\n- Synophrys\n- Delayed speech and language development\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Exotropia\n- Synophrys\n- Delayed speech and language development\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Exotropia\n- Synophrys\n- Delayed speech and language development\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Joint laxity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Splenomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait ataxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait ataxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait ataxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Gait ataxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Low-set ears\n- Blue sclerae\n- Long palpebral fissure\n- Nystagmus\n- Pectus excavatum\n- Hypothyroidism\n- Hirsutism\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Ventricular septal defect\n- Right ventricular hypertrophy\n- Abnormal facial shape\n- Pulmonary arterial hypertension\n- Emphysema\n- Pneumothorax\n- Sparse scalp hair\n- Tortuous cerebral arteries\n- Right ventricular dilatation\n- Depressed nasal bridge\n- Broad eyebrow\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/08839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Scoliosis\n- Attention deficit hyperactivity disorder\n- Gastrostomy tube feeding in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/08841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/08842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/08843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/08844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Small for gestational age\n- Postnatal growth retardation\n- Mild global developmental delay\n- Primary microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/08845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Macrocephaly\n- Coarse facial features\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Myopia\n- Hypertrichosis\n- Global developmental delay\n- Large for gestational age\n- Dilated cardiomyopathy\n- Pericardial effusion\n- Hepatomegaly\n- Aplasia\/Hypoplasia of the distal phalanges of the hand\n- Aplasia\/Hypoplasia of the distal phalanges of the toes\n- Thick vermilion border\n- Distal joint laxity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/08846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Macrotia\n- Bulbous nose\n- Strabismus\n- Deeply set eye\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Gynecomastia\n- Decreased response to growth hormone stimulation test\n- Acanthosis nigricans\n- Broad palm\n- Intellectual disability\n- Seizure\n- Broad foot\n- Short foot\n- Short toe\n- Hypoglycemia\n- Porencephalic cyst\n- Sparse body hair\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Periventricular leukomalacia\n- Impaired pain sensation\n- Large earlobe\n- Keloids\n- Delayed fine motor development\n- Posterior pituitary hypoplasia\n- Skin-picking\n- Thick vermilion border\n- Abdominal obesity\n- Intraventricular hemorrhage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Deeply set eye\n- Epicanthus inversus\n- Hypermetropia\n- Nystagmus\n- Delayed speech and language development\n- Tapered finger\n- Spastic diplegia\n- Truncal obesity\n- Delayed gross motor development\n- Clumsiness\n- Intellectual disability, moderate\n- Poor head control\n- Focal-onset seizure\n- Short finger\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Pelvic kidney\n- High palate\n- Hearing impairment\n- Macrotia\n- Nystagmus\n- Delayed speech and language development\n- Decreased response to growth hormone stimulation test\n- Tapered finger\n- Delayed gross motor development\n- Inverted nipples\n- Clinodactyly of the 5th finger\n- Short stature\n- Short 4th toe\n- Ankyloglossia\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Pelvic kidney\n- High palate\n- Hearing impairment\n- Macrotia\n- Nystagmus\n- Delayed speech and language development\n- Decreased response to growth hormone stimulation test\n- Tapered finger\n- Delayed gross motor development\n- Inverted nipples\n- Clinodactyly of the 5th finger\n- Short stature\n- Short 4th toe\n- Ankyloglossia\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Keloids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Melanocytic nevus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nose\n- Aggressive behavior\n- Gynecomastia\n- Brachydactyly\n- Tapered finger\n- Talipes\n- Large earlobe\n- Intellectual disability, severe\n- Short palpebral fissure\n- Long ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadotropic hypogonadism\n- Underdeveloped nasal alae\n- Deeply set eye\n- Long eyelashes\n- Nasolacrimal duct obstruction\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Delayed puberty\n- Hyperpigmentation of the skin\n- Tapered finger\n- Seizure\n- Hypoplastic toenails\n- Hypoplastic fingernail\n- Short 2nd toe\n- Fine hair\n- Poor head control\n- Short nose\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Depressed nasal bridge\n- Enamel hypomineralization\n- Bilateral sensorineural hearing impairment\n- Feeding difficulties in infancy\n- Medial flaring of the eyebrow\n- Midface retrusion\n- Glue ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hydroureter\n- Thick upper lip vermilion\n- Hypertelorism\n- Hypoplasia of the maxilla\n- Sloping forehead\n- Long philtrum\n- Chronic otitis media\n- Prominent nasal bridge\n- Strabismus\n- Hypermetropia\n- Upslanted palpebral fissure\n- Hypodontia\n- Widely spaced teeth\n- Autistic behavior\n- Delayed speech and language development\n- Abnormality of skin pigmentation\n- Joint hypermobility\n- Umbilical hernia\n- Mitral valve prolapse\n- Patent foramen ovale\n- Short toe\n- Talipes\n- Sparse body hair\n- Hip dislocation\n- Clinodactyly of the 5th finger\n- Increased body weight\n- Dermal atrophy\n- 4-5 toe syndactyly\n- Short middle phalanx of finger\n- Axial hypotonia\n- Large earlobe\n- Short 4th metacarpal\n- Short 5th metacarpal\n- Odontoma\n- Dens in dente\n- Fetal distress\n- Keratosis pilaris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick upper lip vermilion\n- Hypertelorism\n- Low-set ears\n- Recurrent otitis media\n- Anteverted nares\n- Strabismus\n- Thick eyebrow\n- Synophrys\n- Conical tooth\n- Delayed speech and language development\n- Acanthosis nigricans\n- Abnormality of skin pigmentation\n- Brachydactyly\n- Tapered finger\n- Global developmental delay\n- Hypertonia\n- Abnormality of the musculature of the lower limbs\n- Umbilical hernia\n- Neonatal hypoglycemia\n- Hypothermia\n- Sparse scalp hair\n- Sleep disturbance\n- Scoliosis\n- Downturned corners of mouth\n- Short nose\n- Gowers sign\n- Clinodactyly of the 5th finger\n- Short stature\n- Hyperactive patellar reflex\n- Calf muscle hypoplasia\n- Large earlobe\n- High anterior hairline\n- Broad hallux\n- Delayed fine motor development\n- Deviation of toes\n- Dorsal hirsutism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Conductive hearing impairment\n- Ptosis\n- Anxiety\n- Delayed speech and language development\n- Primary amenorrhea\n- Hyperpigmentation of the skin\n- Intellectual disability\n- Umbilical hernia\n- Talipes\n- Spontaneous pneumothorax\n- Ventriculomegaly\n- Delayed gross motor development\n- Sparse scalp hair\n- Hip dislocation\n- Obstructive sleep apnea\n- Increased nuchal translucency\n- Enlarged cerebellum\n- Mild myopia\n- Periventricular white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Conductive hearing impairment\n- Ptosis\n- Anxiety\n- Delayed speech and language development\n- Primary amenorrhea\n- Hyperpigmentation of the skin\n- Intellectual disability\n- Umbilical hernia\n- Talipes\n- Spontaneous pneumothorax\n- Ventriculomegaly\n- Delayed gross motor development\n- Sparse scalp hair\n- Hip dislocation\n- Obstructive sleep apnea\n- Increased nuchal translucency\n- Enlarged cerebellum\n- Mild myopia\n- Periventricular white matter hyperintensities\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Prominent supraorbital ridges\n- Sloping forehead\n- Macrotia\n- Narrow nose\n- Anteverted nares\n- Deeply set eye\n- Widely spaced teeth\n- Autism\n- Delayed speech and language development\n- Hemangioma\n- Global developmental delay\n- Frontal bossing\n- Constipation\n- Delayed gross motor development\n- Polyphagia\n- Obstructive sleep apnea\n- Short nose\n- Clinodactyly of the 5th finger\n- Short middle phalanx of the 5th finger\n- Short distal phalanx of the 5th finger\n- Delayed fine motor development\n- Chronic sinusitis\n- Hooded eyelid\n- Irregular dentition\n- Narrow palpebral fissure\n- Oral-pharyngeal dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Amenorrhea\n- Macrocephaly\n- Coarse facial features\n- Long philtrum\n- Periorbital fullness\n- Delayed speech and language development\n- Tapered finger\n- Broad foot\n- Hypoplastic toenails\n- Sandal gap\n- Hypoplasia of the corpus callosum\n- Intellectual disability, moderate\n- Cavum septum pellucidum\n- Short nose\n- Increased body weight\n- Prolonged neonatal jaundice\n- Large earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/08860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/08872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Prominent supraorbital ridges\n- Short neck\n- Conjunctival telangiectasia\n- Pectus carinatum\n- Frontal bossing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Short neck\n- Irritability\n- Frontal bossing\n- Corneal opacity\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Chronic otitis media\n- Delayed speech and language development\n- Global developmental delay\n- Hepatosplenomegaly\n- Umbilical hernia\n- Frontal bossing\n- Lymphadenopathy\n- Recurrent upper respiratory tract infections\n- Abnormality of the tympanic membrane\n- Increased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Coarse facial features\n- Epicanthus\n- Hearing impairment\n- Wide nasal bridge\n- Strabismus\n- Pectus carinatum\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Hepatosplenomegaly\n- Umbilical hernia\n- Recurrent respiratory infections\n- Depressed nasal bridge\n- Lumbar kyphosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Tall stature\n- Coarse facial features\n- Sensorineural hearing impairment\n- Delayed speech and language development\n- Pectus carinatum\n- Dysostosis multiplex\n- Broad metacarpals\n- Intellectual disability\n- Umbilical hernia\n- Kyphoscoliosis\n- Kyphosis\n- Thoracolumbar kyphosis\n- Protruding tongue\n- Anterior wedging of T12\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Hearing impairment\n- Short neck\n- Synophrys\n- Widely spaced teeth\n- Delayed speech and language development\n- Osteopenia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Cerebellar atrophy\n- Hyperreflexia\n- Hallux valgus\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Language impairment\n- Highly arched eyebrow\n- Depressed nasal bridge\n- Periventricular white matter hyperintensities\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Wide nasal bridge\n- Short neck\n- Delayed speech and language development\n- Global developmental delay\n- Highly arched eyebrow\n- Depressed nasal bridge\n- Prominent forehead\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Short neck\n- Intellectual disability\n- Global developmental delay\n- Absent speech\n- Highly arched eyebrow\n- Prominent forehead\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Short neck\n- Highly arched eyebrow\n- Concave nasal ridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Short neck\n- Highly arched eyebrow\n- Concave nasal ridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Short neck\n- Highly arched eyebrow\n- Concave nasal ridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Short neck\n- Highly arched eyebrow\n- Concave nasal ridge\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Hearing impairment\n- Delayed speech and language development\n- Hypoplastic ilia\n- Intellectual disability\n- Vacuolated lymphocytes\n- Hepatomegaly\n- Coxa valga\n- Thickened calvaria\n- Flared iliac wing\n- Hypoplastic acetabulae\n- Ovoid vertebral bodies\n- Proximal tapering of metacarpals\n- Tubular metacarpal bones\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Ptosis\n- Cataract\n- Delayed speech and language development\n- Dysostosis multiplex\n- Intellectual disability\n- Seizure\n- Motor delay\n- Hypertonia\n- Hyperreflexia\n- Hepatosplenomegaly\n- Vacuolated lymphocytes\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Coxa valga\n- Kyphoscoliosis\n- Recurrent upper respiratory tract infections\n- Kyphosis\n- Metaphyseal widening\n- Proximal tapering of metacarpals\n- Increased head circumference\n- Infantile hydrocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Ptosis\n- Cataract\n- Delayed speech and language development\n- Dysostosis multiplex\n- Intellectual disability\n- Seizure\n- Motor delay\n- Hypertonia\n- Hyperreflexia\n- Hepatosplenomegaly\n- Vacuolated lymphocytes\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Coxa valga\n- Kyphoscoliosis\n- Recurrent upper respiratory tract infections\n- Kyphosis\n- Metaphyseal widening\n- Proximal tapering of metacarpals\n- Increased head circumference\n- Infantile hydrocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Ptosis\n- Cataract\n- Delayed speech and language development\n- Dysostosis multiplex\n- Intellectual disability\n- Seizure\n- Motor delay\n- Hypertonia\n- Hyperreflexia\n- Hepatosplenomegaly\n- Vacuolated lymphocytes\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Coxa valga\n- Kyphoscoliosis\n- Recurrent upper respiratory tract infections\n- Kyphosis\n- Metaphyseal widening\n- Proximal tapering of metacarpals\n- Increased head circumference\n- Infantile hydrocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Brachycephaly\n- Coarse facial features\n- Hypertelorism\n- Ptosis\n- Cataract\n- Delayed speech and language development\n- Dysostosis multiplex\n- Intellectual disability\n- Seizure\n- Motor delay\n- Hypertonia\n- Hyperreflexia\n- Hepatosplenomegaly\n- Vacuolated lymphocytes\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Coxa valga\n- Kyphoscoliosis\n- Recurrent upper respiratory tract infections\n- Kyphosis\n- Metaphyseal widening\n- Proximal tapering of metacarpals\n- Increased head circumference\n- Infantile hydrocele\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Macroglossia\n- Gingival overgrowth\n- High palate\n- Coarse facial features\n- Hypertelorism\n- Hearing impairment\n- Macrotia\n- Short neck\n- Strabismus\n- Cataract\n- Delayed speech and language development\n- Pectus excavatum\n- Dysostosis multiplex\n- Global developmental delay\n- Umbilical hernia\n- Hypertrophic cardiomyopathy\n- Frontal bossing\n- Recurrent respiratory infections\n- Hepatomegaly\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Protruding tongue\n- Mongolian blue spot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Macroglossia\n- Gingival overgrowth\n- High palate\n- Coarse facial features\n- Hypertelorism\n- Hearing impairment\n- Macrotia\n- Short neck\n- Strabismus\n- Cataract\n- Delayed speech and language development\n- Pectus excavatum\n- Dysostosis multiplex\n- Global developmental delay\n- Umbilical hernia\n- Hypertrophic cardiomyopathy\n- Frontal bossing\n- Recurrent respiratory infections\n- Hepatomegaly\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Protruding tongue\n- Mongolian blue spot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Macroglossia\n- Gingival overgrowth\n- High palate\n- Coarse facial features\n- Hypertelorism\n- Hearing impairment\n- Macrotia\n- Short neck\n- Strabismus\n- Cataract\n- Delayed speech and language development\n- Pectus excavatum\n- Dysostosis multiplex\n- Global developmental delay\n- Umbilical hernia\n- Hypertrophic cardiomyopathy\n- Frontal bossing\n- Recurrent respiratory infections\n- Hepatomegaly\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Protruding tongue\n- Mongolian blue spot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Macroglossia\n- Gingival overgrowth\n- High palate\n- Coarse facial features\n- Hypertelorism\n- Hearing impairment\n- Macrotia\n- Short neck\n- Strabismus\n- Cataract\n- Delayed speech and language development\n- Pectus excavatum\n- Dysostosis multiplex\n- Global developmental delay\n- Umbilical hernia\n- Hypertrophic cardiomyopathy\n- Frontal bossing\n- Recurrent respiratory infections\n- Hepatomegaly\n- Intellectual disability, moderate\n- Short stature\n- Depressed nasal bridge\n- Protruding tongue\n- Mongolian blue spot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Strabismus\n- Delayed speech and language development\n- Ataxia\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Hepatosplenomegaly\n- Intellectual disability, moderate\n- Genu valgum\n- Spondylolisthesis\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Coarse facial features\n- Hypertelorism\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Sensorineural hearing impairment\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Umbilical hernia\n- Hepatomegaly\n- Delayed skeletal maturation\n- Increased body weight\n- Depressed nasal bridge\n- Increased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Recurrent otitis media\n- Short neck\n- Widely spaced teeth\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Asthma\n- Hepatomegaly\n- Drooling\n- Frequent falls\n- Clinodactyly of the 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Coarse facial features\n- Low anterior hairline\n- Hearing impairment\n- Anteverted nares\n- Short neck\n- Global developmental delay\n- Hepatomegaly\n- Increased size of the mandible\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/08900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/08902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Frontal bossing\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Dysostosis multiplex\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Facial hypertrichosis\n- Depressed nasal bridge\n- Corneal opacity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Facial hypertrichosis\n- Depressed nasal bridge\n- Corneal opacity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Kyphosis\n- Joint contracture of the hand\n- Short thorax\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/08913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Joint dislocation\n- Myelopathy\n- Scoliosis\n- Vertebral fusion\n- Short stature\n- Pseudoepiphyses of the metacarpals\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/08914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Cataract\n- Proptosis\n- Myopia\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/08915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Facial asymmetry\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Ptosis\n- Long palpebral fissure\n- Growth delay\n- Large fleshy ears\n- Elevated circulating alkaline phosphatase concentration\n- Clinodactyly of the 5th finger\n- Shortening of all distal phalanges of the fingers\n- Aplasia\/Hypoplasia of the nails\n- Uplifted earlobe\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Facial asymmetry\n- Wide nasal bridge\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Ptosis\n- Long palpebral fissure\n- Growth delay\n- Large fleshy ears\n- Elevated circulating alkaline phosphatase concentration\n- Clinodactyly of the 5th finger\n- Shortening of all distal phalanges of the fingers\n- Aplasia\/Hypoplasia of the nails\n- Uplifted earlobe\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Seizure\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Aganglionic megacolon\n- Shortening of all distal phalanges of the fingers\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/08919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Malar flattening\n- Osteopenia\n- Pathologic fracture\n- Excessive skin wrinkling on dorsum of hands and fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/08924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cutis laxa\n- Intellectual disability\n- Abnormal facial shape\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/08938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Microcephaly\n- Abnormality of the philtrum\n- Narrow forehead\n- Cupped ear\n- Prominent nasal bridge\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Deeply set eye\n- Myopia\n- Widely spaced teeth\n- Single transverse palmar crease\n- Absent speech\n- Broad toe\n- Constipation\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Abnormal caudate nucleus morphology\n- Difficulty walking\n- Tachypnea\n- Episodic tachypnea\n- Short stature\n- Flat occiput\n- Limb undergrowth\n- Broad fingertip\n- Severe global developmental delay\n- Thick vermilion border\n- Hypoplastic hippocampus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Microcephaly\n- Abnormality of the philtrum\n- Narrow forehead\n- Cupped ear\n- Prominent nasal bridge\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Deeply set eye\n- Myopia\n- Widely spaced teeth\n- Single transverse palmar crease\n- Absent speech\n- Broad toe\n- Constipation\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Abnormal caudate nucleus morphology\n- Difficulty walking\n- Tachypnea\n- Episodic tachypnea\n- Short stature\n- Flat occiput\n- Limb undergrowth\n- Broad fingertip\n- Severe global developmental delay\n- Thick vermilion border\n- Hypoplastic hippocampus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Microcephaly\n- Abnormality of the philtrum\n- Narrow forehead\n- Cupped ear\n- Prominent nasal bridge\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Deeply set eye\n- Myopia\n- Widely spaced teeth\n- Single transverse palmar crease\n- Absent speech\n- Broad toe\n- Constipation\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Abnormal caudate nucleus morphology\n- Difficulty walking\n- Tachypnea\n- Episodic tachypnea\n- Short stature\n- Flat occiput\n- Limb undergrowth\n- Broad fingertip\n- Severe global developmental delay\n- Thick vermilion border\n- Hypoplastic hippocampus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Microcephaly\n- Abnormality of the philtrum\n- Narrow forehead\n- Cupped ear\n- Prominent nasal bridge\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Deeply set eye\n- Myopia\n- Widely spaced teeth\n- Single transverse palmar crease\n- Absent speech\n- Broad toe\n- Constipation\n- Bilateral tonic-clonic seizure\n- Hypoplasia of the corpus callosum\n- Exaggerated cupid's bow\n- Abnormal caudate nucleus morphology\n- Difficulty walking\n- Tachypnea\n- Episodic tachypnea\n- Short stature\n- Flat occiput\n- Limb undergrowth\n- Broad fingertip\n- Severe global developmental delay\n- Thick vermilion border\n- Hypoplastic hippocampus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Short philtrum\n- Narrow forehead\n- Cupped ear\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Absent speech\n- Small for gestational age\n- Slender build\n- Apnea\n- Ventriculomegaly\n- Intellectual disability, profound\n- Aganglionic megacolon\n- Exaggerated cupid's bow\n- Short stature\n- Intermittent hyperventilation\n- Focal-onset seizure\n- Limb undergrowth\n- Broad fingertip\n- Hypopigmented macule\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Short philtrum\n- Narrow forehead\n- Cupped ear\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Absent speech\n- Small for gestational age\n- Slender build\n- Apnea\n- Ventriculomegaly\n- Intellectual disability, profound\n- Aganglionic megacolon\n- Exaggerated cupid's bow\n- Short stature\n- Intermittent hyperventilation\n- Focal-onset seizure\n- Limb undergrowth\n- Broad fingertip\n- Hypopigmented macule\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Short philtrum\n- Narrow forehead\n- Cupped ear\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Absent speech\n- Small for gestational age\n- Slender build\n- Apnea\n- Ventriculomegaly\n- Intellectual disability, profound\n- Aganglionic megacolon\n- Exaggerated cupid's bow\n- Short stature\n- Intermittent hyperventilation\n- Focal-onset seizure\n- Limb undergrowth\n- Broad fingertip\n- Hypopigmented macule\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Short philtrum\n- Narrow forehead\n- Cupped ear\n- Convex nasal ridge\n- Wide nose\n- Flared nostrils\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Absent speech\n- Small for gestational age\n- Slender build\n- Apnea\n- Ventriculomegaly\n- Intellectual disability, profound\n- Aganglionic megacolon\n- Exaggerated cupid's bow\n- Short stature\n- Intermittent hyperventilation\n- Focal-onset seizure\n- Limb undergrowth\n- Broad fingertip\n- Hypopigmented macule\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureteropelvic junction obstruction\n- Hydronephrosis\n- Wide mouth\n- Microcephaly\n- Macrotia\n- Anteverted nares\n- Deeply set eye\n- Global developmental delay\n- Absent speech\n- Overlapping toe\n- Hypoplasia of the corpus callosum\n- Highly arched eyebrow\n- 2-4 toe cutaneous syndactyly\n- Cerebellar dysplasia\n- Bilateral single transverse palmar creases\n- Vertical nystagmus\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Micrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Prominent nose\n- Reduced eye contact\n- Global developmental delay\n- Generalized hypotonia\n- Cholestasis\n- Ventricular septal defect\n- Atrial septal defect\n- Endocardial fibroelastosis\n- Polysplenia\n- Thrombocytosis\n- Hypoplasia of the corpus callosum\n- Respiratory failure\n- Short stature\n- Decreased body weight\n- Extrahepatic biliary duct atresia\n- Broad fingertip\n- Arrhythmia\n- Thin eyebrow\n- Long fingers\n- Duodenal stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thickened helices\n- Prominent nasal bridge\n- Prominent nose\n- Flared nostrils\n- Strabismus\n- Deeply set eye\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Single transverse palmar crease\n- EEG abnormality\n- Supernumerary nipple\n- Scoliosis\n- Secondary microcephaly\n- Moderate postnatal growth retardation\n- Abnormal helix morphology\n- Severe global developmental delay\n- Tented philtrum\n- Thick vermilion border\n- Thin eyebrow\n- Small hand\n- Brain imaging abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thickened helices\n- Prominent nasal bridge\n- Prominent nose\n- Flared nostrils\n- Strabismus\n- Deeply set eye\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Single transverse palmar crease\n- Seizure\n- EEG abnormality\n- Sleep disturbance\n- Hyperventilation\n- Secondary microcephaly\n- Moderate postnatal growth retardation\n- Abnormal helix morphology\n- Severe global developmental delay\n- Tented philtrum\n- Thick vermilion border\n- Thin eyebrow\n- Small hand\n- Brain imaging abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thickened helices\n- Prominent nasal bridge\n- Prominent nose\n- Flared nostrils\n- Strabismus\n- Deeply set eye\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Single transverse palmar crease\n- Seizure\n- EEG abnormality\n- Sleep disturbance\n- Hyperventilation\n- Secondary microcephaly\n- Moderate postnatal growth retardation\n- Abnormal helix morphology\n- Severe global developmental delay\n- Tented philtrum\n- Thick vermilion border\n- Thin eyebrow\n- Small hand\n- Brain imaging abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Thickened helices\n- Prominent nasal bridge\n- Prominent nose\n- Flared nostrils\n- Strabismus\n- Deeply set eye\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Single transverse palmar crease\n- Seizure\n- EEG abnormality\n- Supernumerary nipple\n- Hyperventilation\n- Secondary microcephaly\n- Moderate postnatal growth retardation\n- Abnormal helix morphology\n- Severe global developmental delay\n- Tented philtrum\n- Thick vermilion border\n- Unilateral cryptorchidism\n- Thin eyebrow\n- Clubbing of fingers\n- Small hand\n- Brain imaging abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Thickened helices\n- Prominent nasal bridge\n- Prominent nose\n- Flared nostrils\n- Strabismus\n- Deeply set eye\n- Widely spaced teeth\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Single transverse palmar crease\n- Seizure\n- EEG abnormality\n- Hyperventilation\n- Secondary microcephaly\n- Moderate postnatal growth retardation\n- Abnormal helix morphology\n- Severe global developmental delay\n- Tented philtrum\n- Thick vermilion border\n- Unilateral cryptorchidism\n- Thin eyebrow\n- Small hand\n- Fetal nuchal edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prominent nasal bridge\n- Prominent nose\n- Deeply set eye\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Cyanosis\n- Seizure\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Episodic tachypnea\n- Muscle stiffness\n- Severe global developmental delay\n- Arrhythmia\n- Dermoid cyst\n- Circumoral cyanosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Convex nasal ridge\n- Wide nose\n- Myopia\n- Nystagmus\n- Carious teeth\n- Oligodontia\n- Delayed speech and language development\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Short foot\n- Broad-based gait\n- 2-3 toe syndactyly\n- Prominent metopic ridge\n- Axial hypotonia\n- Esodeviation\n- Auditory sensitivity\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Convex nasal ridge\n- Wide nose\n- Myopia\n- Nystagmus\n- Carious teeth\n- Oligodontia\n- Delayed speech and language development\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Short foot\n- Broad-based gait\n- 2-3 toe syndactyly\n- Prominent metopic ridge\n- Axial hypotonia\n- Esodeviation\n- Auditory sensitivity\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Convex nasal ridge\n- Wide nose\n- Myopia\n- Nystagmus\n- Carious teeth\n- Oligodontia\n- Delayed speech and language development\n- Single transverse palmar crease\n- Tapered finger\n- Global developmental delay\n- Short foot\n- Broad-based gait\n- 2-3 toe syndactyly\n- Prominent metopic ridge\n- Axial hypotonia\n- Esodeviation\n- Auditory sensitivity\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Dolichocephaly\n- Epicanthus\n- Mandibular prognathia\n- Abnormal repetitive mannerisms\n- Cyanosis\n- Seizure\n- Absent speech\n- Constipation\n- Exaggerated cupid's bow\n- Episodic tachypnea\n- Sudden episodic apnea\n- Decreased body weight\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Dolichocephaly\n- Epicanthus\n- Mandibular prognathia\n- Abnormal repetitive mannerisms\n- Cyanosis\n- Seizure\n- Absent speech\n- Constipation\n- Exaggerated cupid's bow\n- Episodic tachypnea\n- Sudden episodic apnea\n- Decreased body weight\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- High palate\n- Hypertelorism\n- Smooth philtrum\n- Convex nasal ridge\n- Esotropia\n- Sparse eyelashes\n- Horizontal nystagmus\n- Abnormal repetitive mannerisms\n- Pectus excavatum\n- Single transverse palmar crease\n- Facial erythema\n- Tapered finger\n- Hypotonia\n- Global developmental delay\n- Oligohydramnios\n- Gastroesophageal reflux\n- Aphasia\n- Decreased body weight\n- Finger syndactyly\n- Erythema\n- Midface retrusion\n- Productive cough\n- Clubbing of fingers\n- Recurrent upper and lower respiratory tract infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Brachycephaly\n- Full cheeks\n- Narrow forehead\n- Sensorineural hearing impairment\n- Bulbous nose\n- Wide nasal bridge\n- Flared nostrils\n- Microdontia\n- Abnormal repetitive mannerisms\n- Pallor\n- Intellectual disability\n- Motor delay\n- Generalized hypotonia\n- Absent speech\n- Failure to thrive\n- Constipation\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Scoliosis\n- Downturned corners of mouth\n- Sudden episodic apnea\n- Hyperventilation\n- Sparse lateral eyebrow\n- Few cafe-au-lait spots\n- Bilateral single transverse palmar creases\n- Thick vermilion border\n- Wide nasal ridge\n- Clinodactyly\n- Palpebral edema\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Bulbous nose\n- Wide nasal bridge\n- Upslanted palpebral fissure\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Widely-spaced maxillary central incisors\n- Bilateral tonic-clonic seizure\n- Delayed CNS myelination\n- Unsteady gait\n- Recurrent upper respiratory tract infections\n- Secondary microcephaly\n- Almond-shaped palpebral fissure\n- Delayed fine motor development\n- High myopia\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/08962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/08964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/08965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Exotropia\n- Depression\n- Parkinsonism\n- Expressive language delay\n- Class III obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/08966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Generalized hypotonia\n- Failure to thrive\n- Ventricular septal defect\n- Delayed gross motor development\n- Bronchomalacia\n- Abnormal bronchus morphology\n- Abnormal drinking behavior\n- Decreased head circumference\n- Bronchoconstriction\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/08967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Cleft palate\n- Microcephaly\n- Sensorineural hearing impairment\n- Hypermetropia\n- Failure to thrive\n- Intrauterine growth retardation\n- Abnormal facial shape\n- Gastroesophageal reflux\n- Pyloric stenosis\n- Proximal placement of thumb\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/08968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prematurely aged appearance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/08969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Short neck\n- Thick eyebrow\n- Narrow chest\n- Premature birth\n- Patent ductus arteriosus\n- Congenital hypertrophy of left ventricle\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/08970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/08973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Acne\n- Seizure\n- Absent speech\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Language impairment\n- Abnormal aggressive, impulsive or violent behavior\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/08974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n- Sleep-wake cycle disturbance\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/08980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hearing impairment\n- Wide nasal bridge\n- Telecanthus\n- Blue irides\n- White forelock\n- Hypoplasia of the iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/08981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- Mandibular prognathia\n- Hypertelorism\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Large hands\n- Hypotonia\n- Long foot\n- Ventriculomegaly\n- Scoliosis\n- Prominent forehead\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macrocephaly\n- Mandibular prognathia\n- Hypertelorism\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Large hands\n- Hypotonia\n- Atrial septal defect\n- Pulmonic stenosis\n- Long foot\n- Accelerated skeletal maturation\n- Prominent forehead\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/08983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/08992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/08999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/09013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- Trismus\n- Mask-like facies\n- Long philtrum\n- Short nose\n- Ulnar deviation of finger\n- Arrhythmia\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Narrow mouth\n- Trismus\n- High palate\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Blepharophimosis\n- Dacryocystitis\n- Hypertonia\n- Flexion contracture\n- Hip dysplasia\n- Joint stiffness\n- Failure to thrive\n- Poor suck\n- Limb hypertonia\n- Neonatal respiratory distress\n- Kyphoscoliosis\n- Short nose\n- Short stature\n- Decreased body weight\n- Absent brainstem auditory responses\n- 2-3 toe syndactyly\n- Ulnar deviation of finger\n- Narrow naris\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Narrow mouth\n- Cleft palate\n- Prominent supraorbital ridges\n- Whistling appearance\n- Micrognathia\n- Depressed nasal ridge\n- Webbed neck\n- Short neck\n- Deeply set eye\n- Adducted thumb\n- Congenital hip dislocation\n- Talipes equinovarus\n- Recurrent upper respiratory tract infections\n- Ulnar deviation of thumb\n- Narrow naris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Narrow mouth\n- Full cheeks\n- Mask-like facies\n- Round face\n- Long philtrum\n- Whistling appearance\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Bilateral ptosis\n- Bilateral talipes equinovarus\n- Vertebral hypoplasia\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Narrow mouth\n- Full cheeks\n- Mask-like facies\n- Round face\n- Long philtrum\n- Whistling appearance\n- Downslanted palpebral fissures\n- Blepharophimosis\n- Bilateral ptosis\n- Bilateral talipes equinovarus\n- Vertebral hypoplasia\n- Underdeveloped supraorbital ridges\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Full cheeks\n- Mask-like facies\n- Long philtrum\n- Whistling appearance\n- Low-set ears\n- Downslanted palpebral fissures\n- Platyspondyly\n- Talipes valgus\n- Clitoral hypertrophy\n- Underdeveloped supraorbital ridges\n- Dimple chin\n- Everted upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Full cheeks\n- Mask-like facies\n- Long philtrum\n- Whistling appearance\n- Low-set ears\n- Downslanted palpebral fissures\n- Platyspondyly\n- Talipes valgus\n- Clitoral hypertrophy\n- Underdeveloped supraorbital ridges\n- Dimple chin\n- Everted upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Prominent supraorbital ridges\n- Long philtrum\n- Whistling appearance\n- Short neck\n- Deeply set eye\n- Downslanted palpebral fissures\n- Talipes equinovarus\n- Overlapping toe\n- Calcaneovalgus deformity\n- Obstructive sleep apnea\n- Cleft ala nasi\n- Short nose\n- Depressed nasal bridge\n- Flat face\n- Camptodactyly\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Prominent supraorbital ridges\n- Long philtrum\n- Whistling appearance\n- Short neck\n- Deeply set eye\n- Downslanted palpebral fissures\n- Talipes equinovarus\n- Overlapping toe\n- Calcaneovalgus deformity\n- Obstructive sleep apnea\n- Cleft ala nasi\n- Short nose\n- Depressed nasal bridge\n- Flat face\n- Camptodactyly\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Microretrognathia\n- Short neck\n- Hypertonia\n- Joint hypermobility\n- Talipes equinovarus\n- Neonatal respiratory distress\n- Abnormality of the lower limb\n- Reduced bone mineral density\n- Stridor\n- Flexion contracture of finger\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Microretrognathia\n- Short neck\n- Hypertonia\n- Joint hypermobility\n- Talipes equinovarus\n- Neonatal respiratory distress\n- Abnormality of the lower limb\n- Reduced bone mineral density\n- Stridor\n- Flexion contracture of finger\n- Nasogastric tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Whistling appearance\n- Micrognathia\n- Webbed neck\n- Short neck\n- Global developmental delay\n- Talipes equinovarus\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Narrow mouth\n- Thin upper lip vermilion\n- Wide anterior fontanel\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Broad nasal tip\n- Conical tooth\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Hepatomegaly\n- Downturned corners of mouth\n- Preauricular pit\n- Wide intermamillary distance\n- Lacrimal duct stenosis\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/09026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Narrow mouth\n- Webbed neck\n- Short neck\n- Strabismus\n- Deeply set eye\n- Axillary pterygium\n- Obesity\n- Toe syndactyly\n- Overlapping toe\n- Low-set nipples\n- Limb joint contracture\n- Short stature\n- Increased body weight\n- Prominent nasolabial fold\n- Limited shoulder movement\n- Wide intermamillary distance\n- Equinovarus deformity\n- Joint contracture of the hand\n- Skin dimple\n- Antalgic gait\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Microglossia\n- High palate\n- Thin vermilion border\n- Full cheeks\n- Mask-like facies\n- Hypertelorism\n- Whistling appearance\n- Low-set ears\n- Protruding ear\n- Underdeveloped nasal alae\n- Deeply set eye\n- Downslanted palpebral fissures\n- Ptosis\n- Hypoplasia of teeth\n- Dental malocclusion\n- Low posterior hairline\n- Kyphoscoliosis\n- Short nose\n- Flexion contracture of toe\n- Limited shoulder movement\n- Equinovarus deformity\n- Bilateral cryptorchidism\n- Ulnar deviation of the hand\n- Limitation of knee mobility\n- Prominent forehead\n- Long upper lip\n- Chin with H-shaped crease\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microglossia\n- High palate\n- Thin vermilion border\n- Epicanthus\n- Mask-like facies\n- Hypertelorism\n- Whistling appearance\n- Low-set ears\n- Overfolded helix\n- Underdeveloped nasal alae\n- Short neck\n- Deeply set eye\n- Downslanted palpebral fissures\n- Microdontia\n- Tooth malposition\n- Dysarthria\n- Talipes equinovarus\n- Short nose\n- Flexion contracture of toe\n- Ulnar deviation of finger\n- Long upper lip\n- Camptodactyly\n- Unilateral cryptorchidism\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Thin upper lip vermilion\n- Epicanthus\n- Narrow forehead\n- Broad nasal tip\n- Short attention span\n- Delayed speech and language development\n- Single transverse palmar crease\n- Global developmental delay\n- Neonatal hypotonia\n- Atrial septal defect\n- Patent ductus arteriosus\n- Sydney crease\n- Cerebral visual impairment\n- Abnormal cardiac catheterization\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/09030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow palate\n- Triangular mouth\n- Thin upper lip vermilion\n- Microcephaly\n- Smooth philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Impaired social interactions\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Neonatal hypotonia\n- Plagiocephaly\n- Neonatal respiratory distress\n- Bilateral single transverse palmar creases\n- Feeding difficulties in infancy\n- Abnormal visual fixation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/09031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Long philtrum\n- Cystic hygroma\n- Reduced tendon reflexes\n- Polyhydramnios\n- Talipes equinovarus\n- Fever\n- Pneumonia\n- Respiratory insufficiency\n- Apnea\n- Limb hypertonia\n- Scoliosis\n- Hip dislocation\n- Depressed nasal bridge\n- Distal arthrogryposis\n- Ulnar deviation of the hand\n- Enlarged naris\n- Chin with H-shaped crease\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Hydrocephalus\n- Macrocephaly\n- Low-set ears\n- Short neck\n- Hypertonia\n- Joint stiffness\n- Polyhydramnios\n- Bell-shaped thorax\n- Talipes equinovarus\n- Pneumonia\n- Hip dislocation\n- Respiratory failure\n- Foot joint contracture\n- Joint contracture of the hand\n- Simplified gyral pattern\n- Chin with H-shaped crease\n- Flexion contracture of finger\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Hydrocephalus\n- Macrocephaly\n- Low-set ears\n- Short neck\n- Hypertonia\n- Joint stiffness\n- Polyhydramnios\n- Bell-shaped thorax\n- Talipes equinovarus\n- Pneumonia\n- Hip dislocation\n- Respiratory failure\n- Foot joint contracture\n- Joint contracture of the hand\n- Simplified gyral pattern\n- Chin with H-shaped crease\n- Flexion contracture of finger\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Epicanthus\n- Mask-like facies\n- Hypertelorism\n- Micrognathia\n- Downslanted palpebral fissures\n- Hip dysplasia\n- Talipes equinovarus\n- Decreased hip abduction\n- Ulnar deviation of finger\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Cleft palate\n- Trismus\n- Full cheeks\n- Long philtrum\n- Whistling appearance\n- Micrognathia\n- Ptosis\n- Blepharophimosis\n- Seizure\n- Hypotonia\n- Polyhydramnios\n- Distal arthrogryposis\n- Severe global developmental delay\n- Neonatal asphyxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Whistling appearance\n- Micrognathia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Hypotonia\n- Polyhydramnios\n- Distal arthrogryposis\n- Postnatal growth retardation\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/09038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/09039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Micrognathia\n- Strabismus\n- Autism\n- Delayed speech and language development\n- Hyperhidrosis\n- Seizure\n- Intellectual disability, mild\n- Motor delay\n- Overlapping toe\n- Sandal gap\n- Attention deficit hyperactivity disorder\n- Prominent ear helix\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent nasal bridge\n- Exotropia\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Broad hallux\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Malar flattening\n- Retrognathia\n- Prominent nasal bridge\n- Telecanthus\n- Delayed speech and language development\n- Intellectual disability, mild\n- Motor delay\n- Transposition of the great arteries\n- Pes planus\n- Broad hallux\n- Cutaneous syndactyly of toes\n- Medial flaring of the eyebrow\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- 3-4 finger cutaneous syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Polycystic kidney dysplasia\n- Microretrognathia\n- Upslanted palpebral fissure\n- Dental crowding\n- Delayed eruption of teeth\n- Delayed speech and language development\n- Constriction of peripheral visual field\n- 2-3 finger syndactyly\n- Intellectual disability\n- Motor delay\n- Constipation\n- Scoliosis\n- Unilateral ptosis\n- Midface retrusion\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Prominent nose\n- Exotropia\n- Delayed speech and language development\n- Slender finger\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Joint hypermobility\n- Sandal gap\n- Thoracic kyphosis\n- Long nose\n- 2-3 toe syndactyly\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Narrow face\n- Epicanthus\n- Smooth philtrum\n- Ptosis\n- Hypermetropia\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Failure to thrive\n- Small for gestational age\n- Hallux valgus\n- Focal impaired awareness seizure\n- Thoracolumbar scoliosis\n- Butterfly vertebrae\n- Prominent metopic ridge\n- Midface retrusion\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Narrow face\n- Epicanthus\n- Smooth philtrum\n- Ptosis\n- Hypermetropia\n- Exotropia\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Failure to thrive\n- Small for gestational age\n- Hallux valgus\n- Focal impaired awareness seizure\n- Thoracolumbar scoliosis\n- Butterfly vertebrae\n- Prominent metopic ridge\n- Midface retrusion\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microglossia\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Retrognathia\n- Hypertelorism\n- Facial asymmetry\n- Triangular face\n- Micrognathia\n- Protruding ear\n- Prominent nose\n- Broad nasal tip\n- Proptosis\n- Long eyelashes\n- Myopia\n- Delayed speech and language development\n- Diabetes mellitus\n- Hyperhidrosis\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hemihypertrophy\n- Hoarse voice\n- Dysphonia\n- Pes planus\n- Hallux valgus\n- Sandal gap\n- Scoliosis\n- Hypercholesterolemia\n- Clinodactyly of the 5th finger\n- Short stature\n- 2-3 toe syndactyly\n- Abnormal left ventricular function\n- Broad lateral eyebrow\n- Abnormality of the palpebral fissures\n- Decreased serum estradiol\n- Feeding difficulties in infancy\n- Hypoplasia of the musculature\n- Broad hallux phalanx\n- Dyslexia\n- Dysgraphia\n- Concomitant strabismus\n- Asthenia\n- Increased body fat percentage\n- Increased intervertebral space\n- Facet joint arthrosis\n- Long nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microglossia\n- High palate\n- Thin upper lip vermilion\n- Microcephaly\n- Retrognathia\n- Hypertelorism\n- Facial asymmetry\n- Triangular face\n- Micrognathia\n- Protruding ear\n- Prominent nose\n- Broad nasal tip\n- Proptosis\n- Long eyelashes\n- Myopia\n- Delayed speech and language development\n- Diabetes mellitus\n- Hyperhidrosis\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Hemihypertrophy\n- Hoarse voice\n- Dysphonia\n- Pes planus\n- Hallux valgus\n- Sandal gap\n- Scoliosis\n- Hypercholesterolemia\n- Clinodactyly of the 5th finger\n- Short stature\n- 2-3 toe syndactyly\n- Abnormal left ventricular function\n- Broad lateral eyebrow\n- Abnormality of the palpebral fissures\n- Decreased serum estradiol\n- Feeding difficulties in infancy\n- Hypoplasia of the musculature\n- Broad hallux phalanx\n- Dyslexia\n- Dysgraphia\n- Concomitant strabismus\n- Asthenia\n- Increased body fat percentage\n- Increased intervertebral space\n- Facet joint arthrosis\n- Long nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Horseshoe kidney\n- Delayed speech and language development\n- Ventricular septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Clinodactyly of the 5th finger\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/09050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cataract\n- Osteopenia\n- Thin skin\n- Cutis laxa\n- Adducted thumb\n- Hypotonia\n- Brisk reflexes\n- Joint laxity\n- Delayed closure of the anterior fontanelle\n- Intrauterine growth retardation\n- Talipes equinovarus\n- Wormian bones\n- Small foramen magnum\n- Hip dislocation\n- Excessive wrinkled skin\n- Postnatal growth retardation\n- Dermal translucency\n- Abnormality of the curvature of the vertebral column\n- Feeding difficulties\n- obsolete Psychomotor retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Cataract\n- Thin skin\n- Cutis laxa\n- Hypotonia\n- Joint laxity\n- Intrauterine growth retardation\n- Vascular tortuosity\n- Os odontoideum\n- Excessive wrinkled skin\n- Postnatal growth retardation\n- Dermal translucency\n- Feeding difficulties\n- obsolete Psychomotor retardation\n- Hernia\n- Dysharmonic bone age\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long eyelashes\n- Synophrys\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long eyelashes\n- Synophrys\n- Highly arched eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Blue irides\n- Hypopigmentation of the skin\n- Hypopigmentation of hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/09055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Cutis laxa\n- obsolete Prominent epicanthal folds\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Long philtrum\n- Cutis laxa\n- obsolete Prominent epicanthal folds\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Long philtrum\n- Anteverted nares\n- Cutis laxa\n- Prominent nasolabial fold\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Macrotia\n- Periorbital wrinkles\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Retrognathia\n- Broad forehead\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Short nose\n- Bitemporal hollowing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micrognathia\n- Posteriorly rotated ears\n- Short neck\n- Ptosis\n- Cutis laxa\n- Joint laxity\n- Frontal bossing\n- Prematurely aged appearance\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Micrognathia\n- Posteriorly rotated ears\n- Short neck\n- Osteoporosis\n- Cutis laxa\n- Joint laxity\n- Prematurely aged appearance\n- Prominent forehead\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrotia\n- Wide nose\n- Downslanted palpebral fissures\n- Cutis laxa\n- Redundant skin\n- Redundant neck skin\n- Setting-sun eye phenomenon\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: diverse\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Progressive microcephaly\n- Short philtrum\n- Broad nasal tip\n- Strabismus\n- Visual impairment\n- Exotropia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Abnormal facial shape\n- Generalized-onset seizure\n- Hypsarrhythmia\n- Inability to walk\n- Short stature\n- Decreased body weight\n- Moderately short stature\n- Intellectual disability, severe\n- Neurodevelopmental delay\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Malar flattening\n- Broad forehead\n- Hearing abnormality\n- Strabismus\n- Cutis laxa\n- Bruising susceptibility\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Bilateral talipes equinovarus\n- Abnormal facial shape\n- Arthrogryposis multiplex congenita\n- Short stature\n- Reduced bone mineral density\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/09121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Malar flattening\n- Broad forehead\n- Hearing abnormality\n- Strabismus\n- Cutis laxa\n- Bruising susceptibility\n- Global developmental delay\n- Joint laxity\n- Failure to thrive\n- Bilateral talipes equinovarus\n- Abnormal facial shape\n- Arthrogryposis multiplex congenita\n- Short stature\n- Reduced bone mineral density\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/09122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Congenital diaphragmatic hernia\n- Osteopenia\n- Cutis laxa\n- Joint laxity\n- Subvalvular aortic stenosis\n- Bilateral talipes equinovarus\n- Abnormal facial shape\n- Pathologic fracture\n- Progeroid facial appearance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Full cheeks\n- Mandibular prognathia\n- Smooth philtrum\n- Bulbous nose\n- Short neck\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Microdontia\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Hypoplastic toenails\n- Neonatal respiratory distress\n- Short nose\n- Delayed fine motor development\n- Midface retrusion\n- Lumbar hypertrichosis\n- Abnormal drinking behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/09138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Cutis laxa\n- Prematurely aged appearance\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Cutis laxa\n- Prematurely aged appearance\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Cutis laxa\n- Prematurely aged appearance\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Adducted thumb\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Adducted thumb\n- Joint laxity\n- Intrauterine growth retardation\n- Hip dislocation\n- Short nose\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Adducted thumb\n- Joint laxity\n- Intrauterine growth retardation\n- Wormian bones\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n- Postnatal growth retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Wormian bones\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Adducted thumb\n- Joint laxity\n- Intrauterine growth retardation\n- Wormian bones\n- Hip dislocation\n- Short nose\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Glaucoma\n- Cutis laxa\n- Joint laxity\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Adducted thumb\n- Joint laxity\n- Intrauterine growth retardation\n- Hip dislocation\n- Central nervous system degeneration\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Hip dislocation\n- Central nervous system degeneration\n- Postnatal growth retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Postnatal growth retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n- Postnatal growth retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n- Postnatal growth retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormality of the face\n- Abnormality of the skeletal system\n- Seizure\n- Global developmental delay\n- Agenesis of corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/09161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/09163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/09164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Macrodontia\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Macrodontia\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the face\n- Abnormal pinna morphology\n- Bulbous nose\n- Hooded eyelid\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Failure to thrive\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/09173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cutis laxa\n- Prematurely aged appearance\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Large fontanelles\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Cutis laxa\n- Pterygium\n- Joint laxity\n- Delayed closure of the anterior fontanelle\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Delayed speech and language development\n- Broad palm\n- Global developmental delay\n- Motor delay\n- Coxa valga\n- Delayed skeletal maturation\n- Dislocated radial head\n- Elevated circulating alkaline phosphatase concentration\n- Postnatal growth retardation\n- Aplasia\/Hypoplasia of the distal phalanx of the 5th finger\n- Intellectual disability, severe\n- Prominent forehead\n- Broad thumb\n- Thick vermilion border\n- Clinodactyly\n- Long thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/09176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n- Macrodontia\n- Large fleshy ears\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Specific learning disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Albinism\n- Ocular albinism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/09180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/09181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/09182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability, mild\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Albinism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Albinism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Blue irides\n- Abnormality of skin pigmentation\n- Abnormality of hair pigmentation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/09186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Albinism\n- Ocular albinism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Progressive microcephaly\n- Short philtrum\n- Broad nasal tip\n- Strabismus\n- Visual impairment\n- Exotropia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Abnormal facial shape\n- Generalized-onset seizure\n- Hypsarrhythmia\n- Inability to walk\n- Short stature\n- Decreased body weight\n- Moderately short stature\n- Intellectual disability, severe\n- Neurodevelopmental delay\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Progressive microcephaly\n- Short philtrum\n- Broad nasal tip\n- Strabismus\n- Visual impairment\n- Exotropia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Abnormal facial shape\n- Generalized-onset seizure\n- Hypsarrhythmia\n- Inability to walk\n- Short stature\n- Decreased body weight\n- Moderately short stature\n- Intellectual disability, severe\n- Neurodevelopmental delay\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Progressive microcephaly\n- Short philtrum\n- Broad nasal tip\n- Strabismus\n- Visual impairment\n- Exotropia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Abnormal facial shape\n- Generalized-onset seizure\n- Hypsarrhythmia\n- Inability to walk\n- Short stature\n- Decreased body weight\n- Moderately short stature\n- Intellectual disability, severe\n- Neurodevelopmental delay\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Progressive microcephaly\n- Short philtrum\n- Broad nasal tip\n- Strabismus\n- Visual impairment\n- Exotropia\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Abnormal facial shape\n- Generalized-onset seizure\n- Hypsarrhythmia\n- Inability to walk\n- Short stature\n- Decreased body weight\n- Moderately short stature\n- Intellectual disability, severe\n- Neurodevelopmental delay\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/09211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micrognathia\n- Abnormality of the middle ear\n- Atresia of the external auditory canal\n- Astigmatism\n- Hyperopic astigmatism\n- Visual impairment\n- Amblyopia\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Abnormal facial shape\n- Severe short stature\n- Decreased body weight\n- Mandibulofacial dysostosis\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Hemifacial hypoplasia\n- Severe conductive hearing impairment\n- Neurodevelopmental delay\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- Abnormal mandible morphology\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Depressed nasal tip\n- Strabismus\n- Downslanted palpebral fissures\n- Visual impairment\n- Optic nerve hypoplasia\n- Periorbital fullness\n- Nystagmus\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Abnormal facial shape\n- Vomiting\n- Gastroesophageal reflux\n- Scoliosis\n- Depressed nasal bridge\n- Lateral ventricle dilatation\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Abnormality of brain morphology\n- Oral aversion\n- Severe conductive hearing impairment\n- Neurodevelopmental delay\n- Wide nasal ridge\n- Hip pain\n- Cautious gait\n- Antalgic gait\n- obsolete Toe walking\n- Cerebral palsy\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Amblyopia\n- Atypical behavior\n- Impaired social interactions\n- Anxiety\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Global developmental delay\n- Abnormal heart morphology\n- Pes planus\n- Repetitive compulsive behavior\n- Impaired tactile sensation\n- Impaired proprioception\n- Intellectual disability, severe\n- Muscular ventricular septal defect\n- Feeding difficulties\n- Neurodevelopmental delay\n- Anisometropia\n- Auditory sensitivity\n- Delayed ability to walk\n- Abnormal emotion\/affect behavior\n- Hyperesthesia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Amblyopia\n- Atypical behavior\n- Impaired social interactions\n- Anxiety\n- Delayed speech and language development\n- Reduced eye contact\n- Intellectual disability\n- Global developmental delay\n- Abnormal heart morphology\n- Pes planus\n- Repetitive compulsive behavior\n- Impaired tactile sensation\n- Impaired proprioception\n- Intellectual disability, severe\n- Muscular ventricular septal defect\n- Feeding difficulties\n- Neurodevelopmental delay\n- Anisometropia\n- Auditory sensitivity\n- Delayed ability to walk\n- Abnormal emotion\/affect behavior\n- Hyperesthesia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Microcephaly\n- Abnormal mandible morphology\n- Retrognathia\n- Facial asymmetry\n- Low-set ears\n- Broad nasal tip\n- Astigmatism\n- Downslanted palpebral fissures\n- Visual impairment\n- Myopia\n- Bicornuate uterus\n- Osteopenia\n- Sacral dimple\n- Intellectual disability\n- Seizure\n- Motor delay\n- Generalized hypotonia\n- Absent speech\n- Patent foramen ovale\n- Talipes equinovarus\n- Constipation\n- Tethered cord\n- Delayed CNS myelination\n- Delayed gross motor development\n- Fine hair\n- Chiari malformation\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Delayed skeletal maturation\n- Fractures of the long bones\n- Spina bifida occulta\n- Mild short stature\n- Short stature\n- Sagittal craniosynostosis\n- Focal white matter lesions\n- Abnormal pons morphology\n- Proximal placement of thumb\n- Short phalanx of finger\n- Patellar subluxation\n- Dermal translucency\n- Broad columella\n- Intellectual disability, severe\n- Abnormal shape of the frontal region\n- Dry hair\n- Primary microcephaly\n- Bilateral ductus arteriosus\n- Abnormality of brain morphology\n- Delayed myelination\n- Dilation of Virchow-Robin spaces\n- Anorectal anomaly\n- Profound global developmental delay\n- Neurodevelopmental delay\n- Auricular pit\n- Alternating exotropia\n- Delayed ability to walk\n- Sparse eyebrow\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Microcephaly\n- Abnormal mandible morphology\n- Retrognathia\n- Facial asymmetry\n- Low-set ears\n- Broad nasal tip\n- Astigmatism\n- Downslanted palpebral fissures\n- Visual impairment\n- Myopia\n- Bicornuate uterus\n- Osteopenia\n- Sacral dimple\n- Intellectual disability\n- Seizure\n- Motor delay\n- Generalized hypotonia\n- Absent speech\n- Patent foramen ovale\n- Talipes equinovarus\n- Constipation\n- Tethered cord\n- Delayed CNS myelination\n- Delayed gross motor development\n- Fine hair\n- Chiari malformation\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Delayed skeletal maturation\n- Fractures of the long bones\n- Spina bifida occulta\n- Mild short stature\n- Short stature\n- Sagittal craniosynostosis\n- Focal white matter lesions\n- Abnormal pons morphology\n- Proximal placement of thumb\n- Short phalanx of finger\n- Patellar subluxation\n- Dermal translucency\n- Broad columella\n- Intellectual disability, severe\n- Abnormal shape of the frontal region\n- Dry hair\n- Primary microcephaly\n- Bilateral ductus arteriosus\n- Abnormality of brain morphology\n- Delayed myelination\n- Dilation of Virchow-Robin spaces\n- Anorectal anomaly\n- Profound global developmental delay\n- Neurodevelopmental delay\n- Auricular pit\n- Alternating exotropia\n- Delayed ability to walk\n- Sparse eyebrow\n- Decreased body mass index\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Visual impairment\n- Optic nerve hypoplasia\n- Atypical behavior\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Abnormal heart morphology\n- Abnormal facial shape\n- Dysphagia\n- Hypoplasia of the corpus callosum\n- Absent nipple\n- Unilateral ptosis\n- Aplasia\/Hypoplasia of the optic nerve\n- Feeding difficulties\n- Abnormal aortic arch morphology\n- Abnormality of brain morphology\n- Neurodevelopmental delay\n- Periventricular white matter hypodensities\n- Abnormality of optic chiasm morphology\n- Auricular pit\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Bulbous nose\n- Wide nasal bridge\n- Visual impairment\n- Optic nerve hypoplasia\n- Atypical behavior\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Abnormal heart morphology\n- Abnormal facial shape\n- Dysphagia\n- Hypoplasia of the corpus callosum\n- Absent nipple\n- Unilateral ptosis\n- Aplasia\/Hypoplasia of the optic nerve\n- Feeding difficulties\n- Abnormal aortic arch morphology\n- Abnormality of brain morphology\n- Neurodevelopmental delay\n- Periventricular white matter hypodensities\n- Abnormality of optic chiasm morphology\n- Auricular pit\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Vesicoureteral reflux\n- Thin vermilion border\n- Abnormal mandible morphology\n- Microretrognathia\n- Hearing impairment\n- Low-set ears\n- Bulbous nose\n- Astigmatism\n- Downslanted palpebral fissures\n- Visual impairment\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Short foot\n- Abnormal facial shape\n- Attention deficit hyperactivity disorder\n- Microtia\n- Metopic synostosis\n- Gastrostomy tube feeding in infancy\n- Midface retrusion\n- Feeding difficulties\n- Neurodevelopmental delay\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Vesicoureteral reflux\n- Thin vermilion border\n- Abnormal mandible morphology\n- Microretrognathia\n- Hearing impairment\n- Low-set ears\n- Bulbous nose\n- Astigmatism\n- Downslanted palpebral fissures\n- Visual impairment\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Short foot\n- Abnormal facial shape\n- Attention deficit hyperactivity disorder\n- Microtia\n- Metopic synostosis\n- Gastrostomy tube feeding in infancy\n- Midface retrusion\n- Feeding difficulties\n- Neurodevelopmental delay\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormal mandible morphology\n- Mandibular prognathia\n- Smooth philtrum\n- Abnormal pinna morphology\n- Small earlobe\n- Triangular nasal tip\n- Optic atrophy\n- Atypical behavior\n- Autism\n- Autistic behavior\n- Delayed speech and language development\n- Multiple lentigines\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Limited elbow extension\n- Ventriculomegaly\n- Intellectual disability, moderate\n- Sleep disturbance\n- Mild short stature\n- Short stature\n- Cerebellar vermis atrophy\n- Focal white matter lesions\n- Almond-shaped palpebral fissure\n- Asymmetry of the mouth\n- Left aortic arch with retroesophageal diverticulum of Kommerell\n- Feeding difficulties\n- Right aortic arch\n- Abnormal aortic arch morphology\n- Flat face\n- Abnormality of brain morphology\n- Small pituitary gland\n- Neurodevelopmental delay\n- Abnormality of optic chiasm morphology\n- Punding\n- Delayed ability to walk\n- Hypoplasia of the olfactory bulb\n- Recurrent hand flapping\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/09237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- Synophrys\n- Global developmental delay\n- Failure to thrive\n- Gastroesophageal reflux\n- Short nose\n- Short 5th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Small scrotum\n- Narrow mouth\n- Microcephaly\n- Facial asymmetry\n- Mixed hearing impairment\n- Strabismus\n- Visual impairment\n- Optic nerve hypoplasia\n- Atypical behavior\n- Delayed speech and language development\n- Hyperactivity\n- 11 pairs of ribs\n- Abnormal skull morphology\n- Delayed ossification of carpal bones\n- Seizure\n- Spasticity\n- Motor delay\n- Abnormal corpus callosum morphology\n- Generalized hypotonia\n- Joint hypermobility\n- Premature birth\n- Abnormal heart morphology\n- Patent ductus arteriosus\n- Subvalvular aortic stenosis\n- Left ventricular hypertrophy\n- Nonimmune hydrops fetalis\n- Congenital thrombocytopenia\n- Abnormal facial shape\n- Hypoplasia of the corpus callosum\n- Frontal upsweep of hair\n- Coxa valga\n- Skull asymmetry\n- Downturned corners of mouth\n- Skeletal muscle atrophy\n- Neonatal hyperbilirubinemia\n- Mild short stature\n- Birth length less than 3rd percentile\n- Abnormality of body weight\n- Decreased body weight\n- Curly eyelashes\n- Contracture of the proximal interphalangeal joint of the 5th finger\n- Abnormal number of hair whorls\n- Prominent forehead\n- Primary microcephaly\n- Feeding difficulties\n- Abnormality of brain morphology\n- Brain atrophy\n- Neurodevelopmental delay\n- Neurodevelopmental abnormality\n- Delayed ability to walk\n- Narrow palpebral fissure\n- Abnormal fear\/anxiety-related behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Small scrotum\n- Narrow mouth\n- Microcephaly\n- Facial asymmetry\n- Mixed hearing impairment\n- Strabismus\n- Visual impairment\n- Optic nerve hypoplasia\n- Atypical behavior\n- Delayed speech and language development\n- Hyperactivity\n- 11 pairs of ribs\n- Abnormal skull morphology\n- Delayed ossification of carpal bones\n- Seizure\n- Spasticity\n- Motor delay\n- Abnormal corpus callosum morphology\n- Generalized hypotonia\n- Joint hypermobility\n- Premature birth\n- Abnormal heart morphology\n- Patent ductus arteriosus\n- Subvalvular aortic stenosis\n- Left ventricular hypertrophy\n- Nonimmune hydrops fetalis\n- Congenital thrombocytopenia\n- Abnormal facial shape\n- Hypoplasia of the corpus callosum\n- Frontal upsweep of hair\n- Coxa valga\n- Skull asymmetry\n- Downturned corners of mouth\n- Skeletal muscle atrophy\n- Neonatal hyperbilirubinemia\n- Mild short stature\n- Birth length less than 3rd percentile\n- Abnormality of body weight\n- Decreased body weight\n- Curly eyelashes\n- Contracture of the proximal interphalangeal joint of the 5th finger\n- Abnormal number of hair whorls\n- Prominent forehead\n- Primary microcephaly\n- Feeding difficulties\n- Abnormality of brain morphology\n- Brain atrophy\n- Neurodevelopmental delay\n- Neurodevelopmental abnormality\n- Delayed ability to walk\n- Narrow palpebral fissure\n- Abnormal fear\/anxiety-related behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Progressive microcephaly\n- Smooth philtrum\n- Posteriorly rotated ears\n- Hearing impairment\n- Sensorineural hearing impairment\n- Depressed nasal ridge\n- Blepharophimosis\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Arthritis\n- Abnormal heart morphology\n- Abnormal aortic valve morphology\n- Bicuspid aortic valve\n- Aortic valve stenosis\n- Wolff-Parkinson-White syndrome\n- Hydrops fetalis\n- Anemia\n- Congenital thrombocytopenia\n- Abnormal facial shape\n- Gastroesophageal reflux\n- Abnormal cerebral ventricle morphology\n- Fine hair\n- Subependymal cysts\n- Small cerebral cortex\n- Aortic root aneurysm\n- Dysplastic pulmonary valve\n- Periventricular cysts\n- High anterior hairline\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Abnormality of brain morphology\n- Neurodevelopmental delay\n- Wide nasal ridge\n- Delayed ability to sit\n- Nasogastric tube feeding\n- Subdural hemorrhage\n- Arachnoid cyst\n- Cyst of the ductus choledochus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Anteverted nares\n- Synophrys\n- Hirsutism\n- Failure to thrive\n- Abnormality of the upper limb\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Synophrys\n- Failure to thrive\n- Abnormality of the upper limb\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Brachycephaly\n- Microcephaly\n- Progressive microcephaly\n- Smooth philtrum\n- Posteriorly rotated ears\n- Hearing impairment\n- Sensorineural hearing impairment\n- Depressed nasal ridge\n- Blepharophimosis\n- Global developmental delay\n- Motor delay\n- Generalized hypotonia\n- Arthritis\n- Abnormal heart morphology\n- Abnormal aortic valve morphology\n- Bicuspid aortic valve\n- Aortic valve stenosis\n- Wolff-Parkinson-White syndrome\n- Hydrops fetalis\n- Anemia\n- Congenital thrombocytopenia\n- Abnormal facial shape\n- Gastroesophageal reflux\n- Abnormal cerebral ventricle morphology\n- Fine hair\n- Subependymal cysts\n- Small cerebral cortex\n- Aortic root aneurysm\n- Dysplastic pulmonary valve\n- Periventricular cysts\n- High anterior hairline\n- Prominent forehead\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Abnormality of brain morphology\n- Neurodevelopmental delay\n- Wide nasal ridge\n- Delayed ability to sit\n- Nasogastric tube feeding\n- Subdural hemorrhage\n- Arachnoid cyst\n- Cyst of the ductus choledochus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Open mouth\n- Abnormal mandible morphology\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Visual impairment\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Abnormal facial shape\n- Exaggerated cupid's bow\n- Clinodactyly of the 5th finger\n- Mild expressive language delay\n- Mild receptive language delay\n- Feeding difficulties\n- Neurodevelopmental delay\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Open mouth\n- Abnormal mandible morphology\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Visual impairment\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Abnormal facial shape\n- Exaggerated cupid's bow\n- Clinodactyly of the 5th finger\n- Mild expressive language delay\n- Mild receptive language delay\n- Feeding difficulties\n- Neurodevelopmental delay\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Open mouth\n- Abnormal mandible morphology\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Visual impairment\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Abnormal facial shape\n- Exaggerated cupid's bow\n- Clinodactyly of the 5th finger\n- Mild expressive language delay\n- Mild receptive language delay\n- Feeding difficulties\n- Neurodevelopmental delay\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Open mouth\n- Abnormal mandible morphology\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Visual impairment\n- Atypical behavior\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Intellectual disability, mild\n- Global developmental delay\n- Abnormal facial shape\n- Exaggerated cupid's bow\n- Clinodactyly of the 5th finger\n- Mild expressive language delay\n- Mild receptive language delay\n- Feeding difficulties\n- Neurodevelopmental delay\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/09248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Synophrys\n- Hand oligodactyly\n- Failure to thrive\n- Abnormality of the upper limb\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Synophrys\n- Hand oligodactyly\n- Failure to thrive\n- Abnormality of the upper limb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Synophrys\n- Intellectual disability\n- Global developmental delay\n- Abnormality of the upper limb\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Anteverted nares\n- Myopia\n- Thick eyebrow\n- Migraine\n- Scoliosis\n- Bowel irritability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/09254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/09255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/09256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/09257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Hearing impairment\n- White forelock\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/09270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Global developmental delay\n- Overgrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/09276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Overgrowth\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/09277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Lobulated tongue\n- Global developmental delay\n- Oligodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/09278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Nystagmus\n- Albinism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Nystagmus\n- Albinism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/09280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macrocephaly\n- Global developmental delay\n- Overgrowth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/09282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Global developmental delay\n- Proportionate short stature\n- Pulmonary artery stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/09285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormality of subcutaneous fat tissue\n- Prominent scalp veins\n- Failure to thrive\n- Progressive alopecia\n- Proportionate short stature\n- Metacarpophalangeal joint contracture\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/09286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Global developmental delay\n- Atrial septal defect\n- Bilateral single transverse palmar creases\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Short clavicles\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/09288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Lobulated tongue\n- Polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/09289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cafe-au-lait spot\n- Axillary freckling\n- Neurofibromas\n- Plexiform neurofibroma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Neurofibromas\n- Multiple cafe-au-lait spots\n- Plexiform neurofibroma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Single transverse palmar crease\n- Hypotonia\n- Global developmental delay\n- Atrial septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/09293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long palpebral fissure\n- Global developmental delay\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/09296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Coarse facial features\n- Global developmental delay\n- Absent speech\n- Failure to thrive\n- Sparse scalp hair\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/09297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Global developmental delay\n- Abnormal heart morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Axillary freckling\n- Relative macrocephaly\n- Multiple cafe-au-lait spots\n- Inguinal freckling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Seizure\n- Global developmental delay\n- Happy demeanor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/09300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Posteriorly rotated ears\n- Wide nose\n- Downslanted palpebral fissures\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Posteriorly rotated ears\n- Wide nose\n- Downslanted palpebral fissures\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Posteriorly rotated ears\n- Wide nose\n- Downslanted palpebral fissures\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Posteriorly rotated ears\n- Wide nose\n- Downslanted palpebral fissures\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Proptosis\n- Juvenile cataract\n- Motor delay\n- Generalized hypotonia\n- Joint hypermobility\n- Mild neurosensory hearing impairment\n- High myopia\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/09305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Proptosis\n- Juvenile cataract\n- Motor delay\n- Generalized hypotonia\n- Joint hypermobility\n- Mild neurosensory hearing impairment\n- High myopia\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/09306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Round face\n- Smooth philtrum\n- Hypoplasia of the maxilla\n- Broad forehead\n- Long philtrum\n- Hearing impairment\n- Low-set ears\n- Prominent nose\n- Webbed neck\n- Short neck\n- Abnormality of the skin\n- Cutis laxa\n- Hyperextensible skin\n- Soft skin\n- Joint dislocation\n- Joint hypermobility\n- Atrial septal defect\n- Cardiomyopathy\n- Patent foramen ovale\n- Pes planus\n- Scoliosis\n- Short stature\n- Low hanging columella\n- Broad thumb\n- Chronic pain\n- Abnormal oral morphology\n- Long thumb\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/09308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/09309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/09310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/09311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/09312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- Hypotonia\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/09313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Failure to thrive\n- Dysphagia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/09314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n- Failure to thrive\n- Dysphagia\n- Elbow hypertrichosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/09315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n- Developmental regression\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/09316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n- Developmental regression\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/09317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- High palate\n- Low anterior hairline\n- Astigmatism\n- Myopia\n- Thick eyebrow\n- Amblyopia\n- Oligodontia\n- Atypical behavior\n- Aggressive behavior\n- Pectus excavatum\n- Irregular menstruation\n- Hypertrichosis\n- Atopic dermatitis\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Hip dysplasia\n- Atrial septal defect\n- Sleep disturbance\n- Scoliosis\n- Short stature\n- Feeding difficulties in infancy\n- Short 5th finger\n- Overweight\n- Neonatal seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- High palate\n- Low anterior hairline\n- Astigmatism\n- Myopia\n- Thick eyebrow\n- Amblyopia\n- Oligodontia\n- Atypical behavior\n- Aggressive behavior\n- Pectus excavatum\n- Irregular menstruation\n- Hypertrichosis\n- Atopic dermatitis\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Hip dysplasia\n- Atrial septal defect\n- Sleep disturbance\n- Scoliosis\n- Short stature\n- Feeding difficulties in infancy\n- Short 5th finger\n- Overweight\n- Neonatal seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Cleft palate\n- High palate\n- Low anterior hairline\n- Astigmatism\n- Myopia\n- Thick eyebrow\n- Amblyopia\n- Oligodontia\n- Atypical behavior\n- Aggressive behavior\n- Pectus excavatum\n- Irregular menstruation\n- Hypertrichosis\n- Atopic dermatitis\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Hip dysplasia\n- Atrial septal defect\n- Sleep disturbance\n- Scoliosis\n- Short stature\n- Feeding difficulties in infancy\n- Short 5th finger\n- Overweight\n- Neonatal seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Low anterior hairline\n- Oval face\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Myopia\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Agenesis of corpus callosum\n- Absent speech\n- Pes planus\n- Low posterior hairline\n- Intellectual disability, moderate\n- Recurrent infections\n- Congenital, generalized hypertrichosis\n- Attention deficit hyperactivity disorder\n- Infantile muscular hypotonia\n- Overweight\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Low anterior hairline\n- Oval face\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Myopia\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Agenesis of corpus callosum\n- Absent speech\n- Pes planus\n- Low posterior hairline\n- Intellectual disability, moderate\n- Recurrent infections\n- Congenital, generalized hypertrichosis\n- Attention deficit hyperactivity disorder\n- Infantile muscular hypotonia\n- Overweight\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Low anterior hairline\n- Oval face\n- Narrow forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Myopia\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Agenesis of corpus callosum\n- Absent speech\n- Pes planus\n- Low posterior hairline\n- Intellectual disability, moderate\n- Recurrent infections\n- Congenital, generalized hypertrichosis\n- Attention deficit hyperactivity disorder\n- Infantile muscular hypotonia\n- Overweight\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Round face\n- Smooth philtrum\n- Hypoplasia of the maxilla\n- Broad forehead\n- Long philtrum\n- Low-set ears\n- Prominent nose\n- Webbed neck\n- Short neck\n- Abnormality of the skin\n- Hyperextensible skin\n- Soft skin\n- Joint hypermobility\n- Abnormality of the cardiovascular system\n- Abnormal mitral valve morphology\n- Pes planus\n- Scoliosis\n- Short stature\n- Low hanging columella\n- Broad thumb\n- Abnormal oral morphology\n- Long thumb\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Triangular face\n- Short neck\n- Keratitis\n- Thick eyebrow\n- Photophobia\n- Oligodontia\n- Atypical behavior\n- Autistic behavior\n- Single transverse palmar crease\n- Hypertrichosis\n- Keratoconjunctivitis sicca\n- Hypotonia\n- Laryngomalacia\n- Pes planus\n- Constipation\n- Intellectual disability, moderate\n- Developmental regression\n- Recurrent infections\n- Short stature\n- Persistence of primary teeth\n- Pain insensitivity\n- Aplasia\/Hypoplasia of the nails\n- Feeding difficulties in infancy\n- Short 5th finger\n- Stridor\n- Low insertion of columella\n- Everted upper lip vermilion\n- Midface retrusion\n- Overhanging nasal tip\n- Exodeviation\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Triangular face\n- Short neck\n- Keratitis\n- Thick eyebrow\n- Photophobia\n- Oligodontia\n- Atypical behavior\n- Autistic behavior\n- Single transverse palmar crease\n- Hypertrichosis\n- Keratoconjunctivitis sicca\n- Hypotonia\n- Laryngomalacia\n- Pes planus\n- Constipation\n- Intellectual disability, moderate\n- Developmental regression\n- Recurrent infections\n- Short stature\n- Persistence of primary teeth\n- Pain insensitivity\n- Aplasia\/Hypoplasia of the nails\n- Feeding difficulties in infancy\n- Short 5th finger\n- Stridor\n- Low insertion of columella\n- Everted upper lip vermilion\n- Midface retrusion\n- Overhanging nasal tip\n- Exodeviation\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Round face\n- Hypoplasia of the maxilla\n- Broad forehead\n- Hearing impairment\n- Brachydactyly\n- Abnormality of the cardiovascular system\n- Ventricular septal defect\n- Coarctation of aorta\n- Scoliosis\n- Abnormal oral morphology\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Low anterior hairline\n- Astigmatism\n- Strabismus\n- Myopia\n- Delayed eruption of teeth\n- Atypical behavior\n- Diabetes mellitus\n- Seizure\n- Hypotonia\n- Motor delay\n- Partial agenesis of the corpus callosum\n- Atrial septal defect\n- Pes planus\n- Pulmonary arterial hypertension\n- Intellectual disability, moderate\n- Congenital, generalized hypertrichosis\n- Persistence of primary teeth\n- Recurrent pneumonia\n- Impaired pain sensation\n- Sparse hair\n- Pes valgus\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the breasts\n- EEG with focal sharp waves\n- obsolete Abnormal malar bone morphology\n- Peripheral edema\n- Short palpebral fissure\n- Keratosis pilaris\n- Flatulence\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Low anterior hairline\n- Astigmatism\n- Strabismus\n- Myopia\n- Delayed eruption of teeth\n- Atypical behavior\n- Diabetes mellitus\n- Seizure\n- Hypotonia\n- Motor delay\n- Partial agenesis of the corpus callosum\n- Atrial septal defect\n- Pes planus\n- Pulmonary arterial hypertension\n- Intellectual disability, moderate\n- Congenital, generalized hypertrichosis\n- Persistence of primary teeth\n- Recurrent pneumonia\n- Impaired pain sensation\n- Sparse hair\n- Pes valgus\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the breasts\n- EEG with focal sharp waves\n- obsolete Abnormal malar bone morphology\n- Peripheral edema\n- Short palpebral fissure\n- Keratosis pilaris\n- Flatulence\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Low anterior hairline\n- Astigmatism\n- Strabismus\n- Myopia\n- Delayed eruption of teeth\n- Atypical behavior\n- Diabetes mellitus\n- Seizure\n- Hypotonia\n- Motor delay\n- Partial agenesis of the corpus callosum\n- Atrial septal defect\n- Pes planus\n- Pulmonary arterial hypertension\n- Intellectual disability, moderate\n- Congenital, generalized hypertrichosis\n- Persistence of primary teeth\n- Recurrent pneumonia\n- Impaired pain sensation\n- Sparse hair\n- Pes valgus\n- Aplasia\/Hypoplasia of the nails\n- Aplasia\/Hypoplasia of the breasts\n- EEG with focal sharp waves\n- obsolete Abnormal malar bone morphology\n- Peripheral edema\n- Short palpebral fissure\n- Keratosis pilaris\n- Flatulence\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Broad forehead\n- Prominent nose\n- Hyperextensible skin\n- Soft skin\n- Joint hypermobility\n- Abnormality of the cardiovascular system\n- Abnormal mitral valve morphology\n- Pes planus\n- Low hanging columella\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Round face\n- Hypoplasia of the maxilla\n- Broad forehead\n- Low-set ears\n- Prominent nose\n- Abnormality of the skin\n- Hyperextensible skin\n- Soft skin\n- Joint hypermobility\n- Abnormality of the cardiovascular system\n- Abnormal mitral valve morphology\n- Cardiomyopathy\n- Pes planus\n- Scoliosis\n- Low hanging columella\n- Broad thumb\n- Long thumb\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Broad face\n- Low anterior hairline\n- Narrow forehead\n- Wide nasal bridge\n- Myopia\n- Hypotelorism\n- Oligodontia\n- Delayed eruption of teeth\n- Dental malocclusion\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Irregular menstruation\n- Hypertrichosis\n- Hypotonia\n- Global developmental delay\n- Anteriorly placed anus\n- Aortic regurgitation\n- Chronic diarrhea\n- Low posterior hairline\n- Intellectual disability, moderate\n- Developmental regression\n- Recurrent bronchitis\n- Persistence of primary teeth\n- Sparse hair\n- Prominent digit pad\n- Camptodactyly\n- Short palpebral fissure\n- Auditory sensitivity\n- Overweight\n- Motor regression\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Broad face\n- Low anterior hairline\n- Narrow forehead\n- Wide nasal bridge\n- Myopia\n- Hypotelorism\n- Oligodontia\n- Delayed eruption of teeth\n- Dental malocclusion\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Irregular menstruation\n- Hypertrichosis\n- Hypotonia\n- Global developmental delay\n- Anteriorly placed anus\n- Aortic regurgitation\n- Chronic diarrhea\n- Low posterior hairline\n- Intellectual disability, moderate\n- Developmental regression\n- Recurrent bronchitis\n- Persistence of primary teeth\n- Sparse hair\n- Prominent digit pad\n- Camptodactyly\n- Short palpebral fissure\n- Auditory sensitivity\n- Overweight\n- Motor regression\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Round face\n- Smooth philtrum\n- Broad forehead\n- Long philtrum\n- Prominent nose\n- Webbed neck\n- Short neck\n- Abnormality of the skin\n- Cutis laxa\n- Hyperextensible skin\n- Soft skin\n- Brachydactyly\n- Joint dislocation\n- Joint hypermobility\n- Abnormality of the cardiovascular system\n- Abnormal mitral valve morphology\n- Cardiomyopathy\n- Abnormal tricuspid valve morphology\n- Pes planus\n- Short stature\n- Low hanging columella\n- Arrhythmia\n- Abnormal oral morphology\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/09335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Retrognathia\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Recurrent otitis media\n- Mixed hearing impairment\n- Bulbous nose\n- Broad neck\n- Astigmatism\n- Deeply set eye\n- Myopia\n- Oligodontia\n- Delayed eruption of primary teeth\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Acne\n- Global developmental delay\n- Motor delay\n- Agenesis of corpus callosum\n- Plagiocephaly\n- Laryngomalacia\n- Constipation\n- Intellectual disability, moderate\n- Developmental regression\n- Scoliosis\n- Recurrent infections\n- Short stature\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Feeding difficulties in infancy\n- Infantile muscular hypotonia\n- Abnormality of pain sensation\n- Unilateral cryptorchidism\n- Short palpebral fissure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Retrognathia\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Recurrent otitis media\n- Mixed hearing impairment\n- Bulbous nose\n- Broad neck\n- Astigmatism\n- Deeply set eye\n- Myopia\n- Oligodontia\n- Delayed eruption of primary teeth\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Acne\n- Global developmental delay\n- Motor delay\n- Agenesis of corpus callosum\n- Plagiocephaly\n- Laryngomalacia\n- Constipation\n- Intellectual disability, moderate\n- Developmental regression\n- Scoliosis\n- Recurrent infections\n- Short stature\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Feeding difficulties in infancy\n- Infantile muscular hypotonia\n- Abnormality of pain sensation\n- Unilateral cryptorchidism\n- Short palpebral fissure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Retrognathia\n- Coarse facial features\n- Low anterior hairline\n- Long philtrum\n- Recurrent otitis media\n- Mixed hearing impairment\n- Bulbous nose\n- Broad neck\n- Astigmatism\n- Deeply set eye\n- Myopia\n- Oligodontia\n- Delayed eruption of primary teeth\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Acne\n- Global developmental delay\n- Motor delay\n- Agenesis of corpus callosum\n- Plagiocephaly\n- Laryngomalacia\n- Constipation\n- Intellectual disability, moderate\n- Developmental regression\n- Scoliosis\n- Recurrent infections\n- Short stature\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Feeding difficulties in infancy\n- Infantile muscular hypotonia\n- Abnormality of pain sensation\n- Unilateral cryptorchidism\n- Short palpebral fissure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Micrognathia\n- Narrow nasal ridge\n- Blue sclerae\n- Delayed speech and language development\n- Osteopenia\n- Pallor\n- Prominent scalp veins\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Delayed skeletal maturation\n- Pathologic fracture\n- Short nose\n- Short stature\n- Enamel hypoplasia\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Micrognathia\n- Narrow nasal ridge\n- Blue sclerae\n- Delayed speech and language development\n- Osteopenia\n- Pallor\n- Prominent scalp veins\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Delayed skeletal maturation\n- Pathologic fracture\n- Short nose\n- Short stature\n- Enamel hypoplasia\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Micrognathia\n- Narrow nasal ridge\n- Blue sclerae\n- Delayed speech and language development\n- Osteopenia\n- Pallor\n- Prominent scalp veins\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Delayed skeletal maturation\n- Pathologic fracture\n- Short nose\n- Short stature\n- Enamel hypoplasia\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Micrognathia\n- Narrow nasal ridge\n- Blue sclerae\n- Delayed speech and language development\n- Osteopenia\n- Pallor\n- Prominent scalp veins\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Delayed skeletal maturation\n- Pathologic fracture\n- Short nose\n- Short stature\n- Enamel hypoplasia\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Micrognathia\n- Narrow nasal ridge\n- Blue sclerae\n- Delayed speech and language development\n- Osteopenia\n- Pallor\n- Prominent scalp veins\n- Joint hypermobility\n- Bilateral talipes equinovarus\n- Delayed skeletal maturation\n- Pathologic fracture\n- Short nose\n- Short stature\n- Enamel hypoplasia\n- Attention deficit hyperactivity disorder\n- Bilateral cryptorchidism\n- High anterior hairline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Malar flattening\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Triangular face\n- Flared nostrils\n- Strabismus\n- Ptosis\n- Myopia\n- Thick eyebrow\n- Atypical behavior\n- Short attention span\n- Delayed speech and language development\n- Hypothyroidism\n- Hyperhidrosis\n- Hypertrichosis\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Abnormal corpus callosum morphology\n- Absent speech\n- Abnormal left ventricle morphology\n- Pes planus\n- Constipation\n- Low posterior hairline\n- Unsteady gait\n- Intellectual disability, moderate\n- Neonatal respiratory distress\n- Scoliosis\n- High, narrow palate\n- Recurrent infections\n- Swan neck-like deformities of the fingers\n- Persistence of primary teeth\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Pes valgus\n- Enlarged naris\n- Abnormality of pain sensation\n- Horizontal eyebrow\n- Feeding difficulties\n- Mild hearing impairment\n- Overweight\n- Motor regression\n- Nasal polyposis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Malar flattening\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Triangular face\n- Flared nostrils\n- Strabismus\n- Ptosis\n- Myopia\n- Thick eyebrow\n- Atypical behavior\n- Short attention span\n- Delayed speech and language development\n- Hypothyroidism\n- Hyperhidrosis\n- Hypertrichosis\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Abnormal corpus callosum morphology\n- Absent speech\n- Abnormal left ventricle morphology\n- Pes planus\n- Constipation\n- Low posterior hairline\n- Unsteady gait\n- Intellectual disability, moderate\n- Neonatal respiratory distress\n- Scoliosis\n- High, narrow palate\n- Recurrent infections\n- Swan neck-like deformities of the fingers\n- Persistence of primary teeth\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Pes valgus\n- Enlarged naris\n- Abnormality of pain sensation\n- Horizontal eyebrow\n- Feeding difficulties\n- Mild hearing impairment\n- Overweight\n- Motor regression\n- Nasal polyposis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Malar flattening\n- Coarse facial features\n- Low anterior hairline\n- Short philtrum\n- Triangular face\n- Flared nostrils\n- Strabismus\n- Ptosis\n- Myopia\n- Thick eyebrow\n- Atypical behavior\n- Short attention span\n- Delayed speech and language development\n- Hypothyroidism\n- Hyperhidrosis\n- Hypertrichosis\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Abnormal corpus callosum morphology\n- Absent speech\n- Abnormal left ventricle morphology\n- Pes planus\n- Constipation\n- Low posterior hairline\n- Unsteady gait\n- Intellectual disability, moderate\n- Neonatal respiratory distress\n- Scoliosis\n- High, narrow palate\n- Recurrent infections\n- Swan neck-like deformities of the fingers\n- Persistence of primary teeth\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Pes valgus\n- Enlarged naris\n- Abnormality of pain sensation\n- Horizontal eyebrow\n- Feeding difficulties\n- Mild hearing impairment\n- Overweight\n- Motor regression\n- Nasal polyposis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Epicanthus\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Hypotelorism\n- Atypical behavior\n- Intellectual disability, mild\n- Neonatal hypotonia\n- Plagiocephaly\n- Constipation\n- Hypocalcemia\n- Enlarged labia minora\n- Thin lower lip vermilion\n- Tented upper lip vermilion\n- Delayed myelination\n- Endometriosis\n- Abnormal eating behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Retrognathia\n- Epicanthus\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Hypotelorism\n- Atypical behavior\n- Intellectual disability, mild\n- Neonatal hypotonia\n- Plagiocephaly\n- Constipation\n- Hypocalcemia\n- Enlarged labia minora\n- Thin lower lip vermilion\n- Tented upper lip vermilion\n- Delayed myelination\n- Endometriosis\n- Abnormal eating behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Submucous cleft hard palate\n- Hypernasal speech\n- Tetralogy of Fallot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/09349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- High palate\n- Cutis laxa\n- Hypotonia\n- Umbilical hernia\n- Emphysema\n- Chronic lung disease\n- Infantile spasms\n- Esodeviation\n- Acute respiratory distress syndrome\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- High palate\n- Cutis laxa\n- Hypotonia\n- Umbilical hernia\n- Emphysema\n- Chronic lung disease\n- Infantile spasms\n- Esodeviation\n- Acute respiratory distress syndrome\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Narrow palate\n- Everted lower lip vermilion\n- Macrocephaly\n- Malar flattening\n- Coarse facial features\n- Low anterior hairline\n- Short neck\n- Photophobia\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Autistic behavior\n- Delayed speech and language development\n- Atopic dermatitis\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Mitral regurgitation\n- Phimosis\n- Pes planus\n- Asthma\n- Intellectual disability, moderate\n- Developmental regression\n- Hypoplastic nipples\n- Recurrent infections\n- Short middle phalanx of the 5th finger\n- Persistence of primary teeth\n- Focal-onset seizure\n- Pes valgus\n- EEG with focal sharp waves\n- Auditory sensitivity\n- Overweight\n- Sickled erythrocytes\n- Alternating exotropia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Everted lower lip vermilion\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Amblyopia\n- Delayed eruption of teeth\n- Atypical behavior\n- Autism\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Multiple lentigines\n- Global developmental delay\n- Motor delay\n- Deep philtrum\n- Constipation\n- Intellectual disability, moderate\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Short stature\n- Persistence of primary teeth\n- Attention deficit hyperactivity disorder\n- Almond-shaped palpebral fissure\n- High anterior hairline\n- Protruding tongue\n- Short palpebral fissure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Malar flattening\n- Coarse facial features\n- Full cheeks\n- Low anterior hairline\n- Facial hypotonia\n- Smooth philtrum\n- Short philtrum\n- Bulbous nose\n- Short neck\n- Thick eyebrow\n- Synophrys\n- Atypical behavior\n- Delayed speech and language development\n- Hyperactivity\n- Seizure\n- Hypotonia\n- Asymmetry of the thorax\n- Phimosis\n- Pes planus\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Highly arched eyebrow\n- Patellar dislocation\n- Clinodactyly of the 5th finger\n- Short stature\n- Preauricular pit\n- Congenital, generalized hypertrichosis\n- Depressed nasal bridge\n- Sparse hair\n- Protruding tongue\n- Midface retrusion\n- Broad chin\n- Feeding difficulties\n- Exodeviation\n- Overweight\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Wide mouth\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Coarse facial features\n- Strabismus\n- Alacrima\n- Myopia\n- Oligodontia\n- Atypical behavior\n- Aggressive behavior\n- Compulsive behaviors\n- Disinhibition\n- Self-mutilation\n- Hypertension\n- Atopic dermatitis\n- Seizure\n- Global developmental delay\n- Hip dysplasia\n- Bilateral tonic-clonic seizure\n- Sparse axillary hair\n- Sparse pubic hair\n- Intellectual disability, moderate\n- Developmental regression\n- Neonatal respiratory distress\n- Scoliosis\n- Recurrent infections\n- Elevated hepatic transaminase\n- Hypercholesterolemia\n- Allergic rhinitis\n- Tricuspid regurgitation\n- Persistence of primary teeth\n- Sparse hair\n- Feeding difficulties in infancy\n- Abnormality of pain sensation\n- Recurrent cystitis\n- Exodeviation\n- Delayed ability to sit\n- Overweight\n- Osteochondroma\n- Delayed ability to walk\n- Nasal polyposis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary incontinence\n- Inguinal hernia\n- Wide mouth\n- Everted lower lip vermilion\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Astigmatism\n- Strabismus\n- Myopia\n- Delayed eruption of teeth\n- Autism\n- Delayed speech and language development\n- Hyperextensibility of the finger joints\n- Hypotonia\n- Global developmental delay\n- Deep philtrum\n- Constipation\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Persistence of primary teeth\n- Attention deficit hyperactivity disorder\n- Almond-shaped palpebral fissure\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Epicanthus\n- Broad philtrum\n- Full cheeks\n- Broad forehead\n- Bulbous nose\n- Astigmatism\n- Thick eyebrow\n- Amblyopia\n- Atypical behavior\n- Autistic behavior\n- Anxiety\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Pes planus\n- Sandal gap\n- Constipation\n- Low posterior hairline\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Sparse hair\n- Feeding difficulties\n- Short palpebral fissure\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Blue sclerae\n- Prominent scalp veins\n- Short nose\n- Premature thelarche\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Blue sclerae\n- Prominent scalp veins\n- Short nose\n- Premature thelarche\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Brachycephaly\n- Blue sclerae\n- Prominent scalp veins\n- Short nose\n- Premature thelarche\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/09374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Myopia\n- Osteopenia\n- Cutis laxa\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Congenital hip dislocation\n- Joint laxity\n- Deep palmar crease\n- Prematurely aged appearance\n- Premature skin wrinkling\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Osteopenia\n- Cutis laxa\n- Adducted thumb\n- Hand clenching\n- Joint laxity\n- Pathologic fracture\n- Deep palmar crease\n- Prematurely aged appearance\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prematurely aged appearance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Abnormality of the nervous system\n- Postaxial hand polydactyly\n- Hypotonia\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Long hallux\n- Delayed CNS myelination\n- Abnormal pattern of respiration\n- Bilateral camptodactyly\n- Central hypoventilation\n- Tube feeding\n- Nuclear cataract\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/09380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Coarse facial features\n- Mandibular prognathia\n- Smooth philtrum\n- Short philtrum\n- Recurrent otitis media\n- Broad nasal tip\n- Broad neck\n- Myopia\n- Upslanted palpebral fissure\n- Atypical behavior\n- Autism\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Goiter\n- Hypertrichosis\n- Seizure\n- Hypotonia\n- Spasticity\n- Global developmental delay\n- Constipation\n- Cerebral atrophy\n- Low posterior hairline\n- EEG abnormality\n- Sleep disturbance\n- Scoliosis\n- Recurrent bronchitis\n- Clinodactyly of the 5th finger\n- Attention deficit hyperactivity disorder\n- Sparse hair\n- Aplasia\/Hypoplasia of the nails\n- Pedal edema\n- Intellectual disability, severe\n- Horizontal eyebrow\n- Feeding difficulties\n- Auditory sensitivity\n- Delayed ability to sit\n- Abnormal visual fixation\n- Overweight\n- Motor regression\n- Hydromyelia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Square face\n- Short philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Astigmatism\n- Long eyelashes\n- Hypermetropia\n- Atypical behavior\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Low frustration tolerance\n- Intellectual disability, mild\n- Global developmental delay\n- Sandal gap\n- Constipation\n- Decreased body weight\n- Broad jaw\n- Socially inappropriate behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Retrognathia\n- Coarse facial features\n- Facial hypotonia\n- Bulbous nose\n- Downslanted palpebral fissures\n- Atypical behavior\n- Compulsive behaviors\n- Delayed speech and language development\n- Agenesis of corpus callosum\n- Hallux valgus\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Recurrent infections\n- Immunodeficiency\n- Persistence of primary teeth\n- High anterior hairline\n- Aplastic\/hypoplastic toenail\n- Atonic seizure\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/09405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/09442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/09459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Global developmental delay\n- Failure to thrive\n- Prominent glabella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/09464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n- Bowing of limbs due to multiple fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n- Global developmental delay\n- Hypertrophic cardiomyopathy\n- Sparse scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Shallow orbits\n- Short stature\n- High myopia\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/09471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Coarse facial features\n- Hirsutism\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Coarse facial features\n- Hepatosplenomegaly\n- Progressive neurologic deterioration\n- Progressive flexion contractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/09477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/09478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Mask-like facies\n- Hand oligodactyly\n- Foot oligodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/09479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n- Thoracic kyphoscoliosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cafe-au-lait spot\n- Axillary freckling\n- Multiple cafe-au-lait spots\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Malar flattening\n- Hearing impairment\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/09482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Malar flattening\n- Hearing impairment\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/09483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/09504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/09505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/09506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/09507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/09508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/09509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/09510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/09511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Broad face\n- Full cheeks\n- Short philtrum\n- Triangular face\n- Posteriorly rotated ears\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Dry skin\n- Global developmental delay\n- Motor delay\n- Pes planus\n- Hypoplastic fingernail\n- Fragile nails\n- Short toe\n- Intellectual disability, moderate\n- Recurrent infections\n- Clinodactyly of the 5th finger\n- Sparse hair\n- Feeding difficulties in infancy\n- Short metacarpal\n- Short metatarsal\n- Prominent forehead\n- Broad chin\n- Delayed menarche\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Narrow palate\n- Thick upper lip vermilion\n- High palate\n- Everted lower lip vermilion\n- Retrognathia\n- Coarse facial features\n- Facial hypotonia\n- Hypertelorism\n- Short philtrum\n- Broad forehead\n- Recurrent otitis media\n- Anteverted nares\n- Short neck\n- Broad neck\n- Astigmatism\n- Downslanted palpebral fissures\n- Hypermetropia\n- Blepharophimosis\n- Atypical behavior\n- Delayed speech and language development\n- Pectus excavatum\n- Abnormal rib morphology\n- Single transverse palmar crease\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Partial agenesis of the corpus callosum\n- Umbilical hernia\n- Pes planus\n- Low posterior hairline\n- Intellectual disability, moderate\n- Attention deficit hyperactivity disorder\n- Narrow nasal tip\n- Short palpebral fissure\n- Camptodactyly of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Low anterior hairline\n- Broad forehead\n- Bulbous nose\n- Atypical behavior\n- Delayed speech and language development\n- Intellectual disability, mild\n- Hallux valgus\n- Anemia\n- Deep philtrum\n- Exaggerated cupid's bow\n- Celiac disease\n- Attention deficit hyperactivity disorder\n- Aplastic\/hypoplastic toenail\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/09514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dentinogenesis imperfecta\n- Recurrent fractures\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Fractures of the long bones\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n- Severe short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Single transverse palmar crease\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/09521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/09522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/09523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Osteopenia\n- Cutis laxa\n- Congenital hip dislocation\n- Joint laxity\n- Umbilical hernia\n- Deep palmar crease\n- Prematurely aged appearance\n- Premature sagging cheeks\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Osteopenia\n- Cutis laxa\n- Pes planus\n- Pathologic fracture\n- Deep palmar crease\n- Prematurely aged appearance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/09525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/09542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hand polydactyly\n- Molar tooth sign on MRI\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/09544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Multiple cafe-au-lait spots\n- Tibial pseudarthrosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Axillary freckling\n- Neurofibromas\n- Multiple cafe-au-lait spots\n- Plexiform neurofibroma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Neurofibromas\n- Multiple cafe-au-lait spots\n- Plexiform neurofibroma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Axillary freckling\n- Multiple cafe-au-lait spots\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/09548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Oculomotor apraxia\n- Hand polydactyly\n- Global developmental delay\n- Molar tooth sign on MRI\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/09549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Proptosis\n- Craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Proptosis\n- Craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cleft palate\n- Global developmental delay\n- Atrial septal defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/09552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Widow's peak\n- Thickened skin\n- Global developmental delay\n- Relative macrocephaly\n- Depressed nasal bridge\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n- Bowing of limbs due to multiple fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macroglossia\n- Hemihypertrophy\n- Umbilical hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Macroglossia\n- Umbilical hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Malar flattening\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/09557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Long face\n- Seizure\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/09558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Broad forehead\n- Downslanted palpebral fissures\n- Sparse scalp hair\n- Deep palmar crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/09559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Downslanted palpebral fissures\n- Sparse scalp hair\n- Short stature\n- Relative macrocephaly\n- Deep palmar crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/09560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hearing impairment\n- Downslanted palpebral fissures\n- Maxillozygomatic hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/09561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Osteopenia\n- Cutis laxa\n- Intellectual disability\n- Intrauterine growth retardation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Malar flattening\n- Triangular face\n- Cataract\n- Cutis laxa\n- Intellectual disability\n- Abnormal corpus callosum morphology\n- Intrauterine growth retardation\n- Large fleshy ears\n- Hip dislocation\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/09563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/09571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the face\n- Wide nasal bridge\n- Atopic dermatitis\n- Seizure\n- Mutism\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Low-set ears\n- Telecanthus\n- Failure to thrive\n- Recurrent infections\n- Decreased circulating antibody level\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Microretrognathia\n- Round face\n- Hypertelorism\n- Anteverted nares\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Anteverted nares\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular face\n- Anteverted nares\n- Delayed speech and language development\n- Failure to thrive\n- Small for gestational age\n- Frontal bossing\n- Respiratory distress\n- Decreased circulating antibody level\n- Depressed nasal bridge\n- Sparse hair\n- Dry hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Shawl scrotum\n- Dolichocephaly\n- Hypertelorism\n- High forehead\n- Prominent nose\n- Telecanthus\n- Frontal bossing\n- Decreased circulating IgA level\n- Immunodeficiency\n- Short nose\n- Abnormal nipple morphology\n- Spotty hyperpigmentation\n- Recurrent pneumonia\n- Multiple cafe-au-lait spots\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/09578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Retrognathia\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Prominent nose\n- Autistic behavior\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Craniosynostosis\n- Poor suck\n- Abnormality of speech or vocalization\n- Delayed gross motor development\n- Highly arched eyebrow\n- Prominent forehead\n- Midface retrusion\n- Feeding difficulties\n- Allergy\n- Narrow palpebral fissure\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/09579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Retrognathia\n- Hypertelorism\n- Long philtrum\n- Low-set ears\n- Prominent nose\n- Autistic behavior\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Craniosynostosis\n- Poor suck\n- Abnormality of speech or vocalization\n- Delayed gross motor development\n- Highly arched eyebrow\n- Prominent forehead\n- Midface retrusion\n- Feeding difficulties\n- Allergy\n- Narrow palpebral fissure\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/09580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Nystagmus\n- Amblyopia\n- Reduced platelet dense granules\n- Nonspecific interstitial pneumonia\n- Rest dyspnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Nystagmus\n- Amblyopia\n- Thrombocytopenia\n- Leukopenia\n- Reduced platelet dense granules\n- Schizophrenia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Strabismus\n- Photophobia\n- Horizontal nystagmus\n- Bruising susceptibility\n- Hypopigmentation of the skin\n- EEG abnormality\n- Attention deficit hyperactivity disorder\n- Reduced visual acuity\n- Hypoplasia of the fovea\n- Absent platelet dense granules\n- Chorioretinal hypopigmentation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- obsolete Primary ovarian failure\n- Short stature\n- Decreased body weight\n- Dilatation of the cerebral artery\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Short ribs\n- Global developmental delay\n- Atrial septal defect\n- Platybasia\n- Abnormality of the cervical spine\n- Short stature\n- Decreased body weight\n- Premature ovarian insufficiency\n- Carpal synostosis\n- Renal atrophy\n- Copper beaten skull\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Rectovaginal fistula\n- Microcephaly\n- Esotropia\n- Anal atresia\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Rectovaginal fistula\n- Microcephaly\n- Esotropia\n- Anal atresia\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Cutis marmorata\n- Hip dysplasia\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Cutis marmorata\n- Hip dysplasia\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hip dysplasia\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Hip dysplasia\n- Vomiting\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Short stature\n- Decreased body weight\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Single transverse palmar crease\n- Hypopigmentation of the skin\n- Sandal gap\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Mild global developmental delay\n- Knee joint hypermobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal dysplasia\n- Microcephaly\n- Short stature\n- Decreased body weight\n- Dysplastic corpus callosum\n- 2-5 toe syndactyly\n- Preaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Bird-like facies\n- Wide nasal bridge\n- Broad nasal tip\n- Telecanthus\n- Ptosis\n- Global developmental delay\n- Small for gestational age\n- Thrombocytopenia\n- Pancytopenia\n- Leukopenia\n- Anemia\n- Recurrent respiratory infections\n- Short stature\n- Severe postnatal growth retardation\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the liver\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Jaundice\n- Hepatosplenomegaly\n- Atrial septal defect\n- Curly hair\n- Elevated circulating alkaline phosphatase concentration\n- Neonatal hyperbilirubinemia\n- Increased serum bile acid concentration\n- Elevated gamma-glutamyltransferase level\n- Elevated circulating aspartate aminotransferase concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Triangular face\n- Deeply set eye\n- Pigmentary retinopathy\n- Posterior embryotoxon\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Right ventricular hypertrophy\n- Secundum atrial septal defect\n- Frontal bossing\n- Recurrent infections\n- Butterfly vertebrae\n- Pulmonary artery stenosis\n- Right ventricular dilatation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Hearing impairment\n- Autism\n- Hypopigmented skin patches\n- Heterochromia iridis\n- Constipation\n- Fatigable weakness\n- Attention deficit hyperactivity disorder\n- White hair\n- Abnormality of the digestive system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/09601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Renal hypoplasia\n- Proteinuria\n- Renal tubular dysfunction\n- Pointed chin\n- Triangular face\n- Hypertension\n- Atrial septal defect\n- Elevated hepatic transaminase\n- Elevated circulating alkaline phosphatase concentration\n- Elevated circulating creatinine concentration\n- Butterfly vertebrae\n- Pulmonary artery stenosis\n- Renal malrotation\n- Persistent left superior vena cava\n- Peripheral edema\n- Elevated gamma-glutamyltransferase level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Broad forehead\n- Low-set ears\n- Deeply set eye\n- Cholestasis\n- Long nose\n- Pulmonary artery stenosis\n- Intrahepatic biliary atresia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Triangular face\n- Broad forehead\n- Protruding ear\n- Deeply set eye\n- Posterior embryotoxon\n- Jaundice\n- Dry skin\n- Xanthomatosis\n- Pulmonary hypoplasia\n- Hepatomegaly\n- Butterfly vertebrae\n- Persistent open anterior fontanelle\n- Widened subarachnoid space\n- Heart murmur\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Nystagmus\n- Global developmental delay\n- Dandy-Walker malformation\n- Plagiocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/09606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Strabismus\n- Global developmental delay\n- Confusion\n- Subcortical cerebral atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/09607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal insufficiency\n- Renal hypoplasia\n- Renal cyst\n- Atrial septal defect\n- Renal tubular acidosis\n- Cholestatic liver disease\n- Pulmonary artery stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal dysplasia\n- Posterior embryotoxon\n- Tetralogy of Fallot\n- Renal tubular acidosis\n- Cholestatic liver disease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal insufficiency\n- Proteinuria\n- Hypertension\n- Microscopic hematuria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Renal insufficiency\n- Proteinuria\n- Renal dysplasia\n- Pulmonic stenosis\n- Peripheral pulmonary artery stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Broad forehead\n- Protruding ear\n- Nevus flammeus\n- Patent ductus arteriosus\n- Right ventricular hypertrophy\n- Right-to-left shunt\n- Pulmonary arterial hypertension\n- Cholestatic liver disease\n- Osteomyelitis\n- Tricuspid regurgitation\n- Hepatic vascular malformations\n- Neonatal sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Broad forehead\n- Deeply set eye\n- Conjunctival icterus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Wide nasal bridge\n- Deeply set eye\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Wide nasal bridge\n- Deeply set eye\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Bulbous nose\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Deeply set eye\n- Cholestasis\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Deeply set eye\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Triangular face\n- Broad forehead\n- Protruding ear\n- Bulbous nose\n- Deeply set eye\n- Upslanted palpebral fissure\n- Jaundice\n- Failure to thrive\n- Abdominal distention\n- Decreased body weight\n- Depressed nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Amenorrhea\n- Microcephaly\n- Long face\n- Pointed chin\n- Triangular face\n- Deeply set eye\n- Posterior embryotoxon\n- Delayed puberty\n- Jaundice\n- Pruritus\n- Cholestasis\n- Failure to thrive\n- Pulmonic stenosis\n- Ventricular hypertrophy\n- Hepatomegaly\n- Elevated hepatic transaminase\n- Elevated circulating alkaline phosphatase concentration\n- Butterfly vertebrae\n- Decreased body weight\n- 2-3 toe syndactyly\n- Intrahepatic biliary atresia\n- Prominent forehead\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Triangular face\n- Broad forehead\n- Deeply set eye\n- Elevated hepatic transaminase\n- Hypercholesterolemia\n- Prominent forehead\n- Heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Depressed nasal tip\n- Deeply set eye\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Depressed nasal tip\n- Deeply set eye\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydroureter\n- Pointed chin\n- Jaundice\n- Hepatosplenomegaly\n- Patent foramen ovale\n- Neonatal respiratory distress\n- Pulmonary artery stenosis\n- Right ventricular dilatation\n- Tricuspid regurgitation\n- Neonatal unconjugated hyperbilirubinemia\n- Prominent forehead\n- Left-to-right shunt\n- Meconium stained amniotic fluid\n- Right atrial enlargement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Bulbous nose\n- Deeply set eye\n- Posterior embryotoxon\n- Jaundice\n- Xanthomatosis\n- Hyperbilirubinemia\n- Butterfly vertebrae\n- Concave nasal ridge\n- Prominent forehead\n- Cardiac total anomalous pulmonary venous connection\n- Increased serum bile acid concentration\n- Heart murmur\n- Elevated gamma-glutamyltransferase level\n- Elevated circulating aspartate aminotransferase concentration\n- Elevated circulating alanine aminotransferase concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/09645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Coarse facial features\n- Broad philtrum\n- Mandibular prognathia\n- Hypertelorism\n- Long philtrum\n- Abnormal earlobe morphology\n- Chronic otitis media\n- Wide nose\n- Strabismus\n- Proptosis\n- Pallor\n- Pyoderma\n- Atopic dermatitis\n- Craniosynostosis\n- Pneumonia\n- Increased circulating IgE level\n- Short stature\n- Prominent nasal tip\n- Persistence of primary teeth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Coarse facial features\n- Mandibular prognathia\n- Facial asymmetry\n- Wide nasal bridge\n- Pallor\n- Atopic dermatitis\n- Short stature\n- Hypochromic microcytic anemia\n- Finger swelling\n- Abscess\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Broad forehead\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n- Deeply set eye\n- Upslanted palpebral fissure\n- Congenital hypothyroidism\n- Jaundice\n- Hypocalcemia\n- Conjugated hyperbilirubinemia\n- Elevated circulating alkaline phosphatase concentration\n- Biliary atresia\n- Prominent forehead\n- Decreased circulating calcifediol concentration\n- Elevated circulating aspartate aminotransferase concentration\n- Elevated circulating alanine aminotransferase concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Broad forehead\n- Bulbous nose\n- Deeply set eye\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pallor\n- Fair hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Oculomotor apraxia\n- Hand polydactyly\n- Global developmental delay\n- Molar tooth sign on MRI\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/09656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hearing impairment\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Severe short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/09661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Hypertelorism\n- Low-set ears\n- Proptosis\n- Failure to thrive\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Congenital contracture\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/09662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/09665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Deeply set eye\n- Thick eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Deeply set eye\n- Thick eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Deeply set eye\n- Thick eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Deeply set eye\n- Thick eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Eczema\n- Failure to thrive\n- Hemolytic anemia\n- Chronic diarrhea\n- Colitis\n- Increased circulating IgE level\n- Death in childhood\n- Recurrent bacterial skin infections\n- Acute respiratory distress syndrome\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Eczema\n- Increased circulating IgE level\n- Pustular rash\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Wide nasal bridge\n- Broad nasal tip\n- Deeply set eye\n- Hemihypertrophy\n- Recurrent infections\n- Prominent forehead\n- Cutaneous abscess\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Facial asymmetry\n- Wide nasal bridge\n- Broad nasal tip\n- Deeply set eye\n- Hemihypertrophy\n- Recurrent infections\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Facial asymmetry\n- Wide nasal bridge\n- Broad nasal tip\n- Deeply set eye\n- Hemihypertrophy\n- Recurrent infections\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Eczema\n- Encephalopathy\n- Bronchiectasis\n- Recurrent respiratory infections\n- Increased circulating IgE level\n- Herpetiform corneal ulceration\n- Death in adolescence\n- Hypereosinophilia\n- Molluscum contagiosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Wide nasal bridge\n- Abnormal dental enamel morphology\n- Eczema\n- Recurrent upper respiratory tract infections\n- Lumbar scoliosis\n- Abnormality of primary teeth\n- Folliculitis\n- Abscess\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Broad nasal tip\n- Deeply set eye\n- Delayed speech and language development\n- Numerous nevi\n- Abnormality of the hand\n- Brachydactyly\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Exaggerated cupid's bow\n- Large earlobe\n- Low hanging columella\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- High palate\n- Low-set ears\n- Broad nasal tip\n- Strabismus\n- Deeply set eye\n- Atypical behavior\n- Autistic behavior\n- Low frustration tolerance\n- Diminished motivation\n- Delayed speech and language development\n- Abnormality of the hand\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Recurrent infections\n- Depressed nasal bridge\n- Large earlobe\n- Low hanging columella\n- Nail-biting\n- Abnormal temper tantrums\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Renal agenesis\n- Wide nasal bridge\n- Ptosis\n- Intellectual disability\n- Neonatal hypotonia\n- Growth delay\n- Abnormal foot morphology\n- Scoliosis\n- Downturned corners of mouth\n- Depressed nasal bridge\n- Tented upper lip vermilion\n- Moderate global developmental delay\n- Midface retrusion\n- Camptodactyly\n- Short palpebral fissure\n- Clinodactyly\n- Ureterovesical junction obstruction\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Otitis media\n- Bulbous nose\n- Deeply set eye\n- Thick eyebrow\n- Atopic dermatitis\n- Joint hypermobility\n- Barrel-shaped chest\n- Pes cavus\n- Diarrhea\n- Kyphoscoliosis\n- Recurrent lower respiratory tract infections\n- Chronic oral candidiasis\n- Onychomycosis\n- Folliculitis\n- Pulmonary pneumatocele\n- Abscess\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Otitis media\n- Bulbous nose\n- Deeply set eye\n- Thick eyebrow\n- Atopic dermatitis\n- Joint hypermobility\n- Barrel-shaped chest\n- Pes cavus\n- Diarrhea\n- Kyphoscoliosis\n- Recurrent lower respiratory tract infections\n- Chronic oral candidiasis\n- Onychomycosis\n- Folliculitis\n- Pulmonary pneumatocele\n- Abscess\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Mandibular prognathia\n- Otitis media\n- Bulbous nose\n- Deeply set eye\n- Thick eyebrow\n- Atopic dermatitis\n- Joint hypermobility\n- Barrel-shaped chest\n- Pes cavus\n- Diarrhea\n- Kyphoscoliosis\n- Recurrent lower respiratory tract infections\n- Chronic oral candidiasis\n- Onychomycosis\n- Folliculitis\n- Pulmonary pneumatocele\n- Abscess\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Anteverted nares\n- Deeply set eye\n- Atypical behavior\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Cerebellar vermis hypoplasia\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Recurrent infections\n- Short nose\n- Depressed nasal bridge\n- Low hanging columella\n- Upper eyelid edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Deeply set eye\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Constipation\n- Exaggerated cupid's bow\n- Recurrent infections\n- obsolete Toe walking\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Deeply set eye\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Intellectual disability, moderate\n- Lumbar hyperlordosis\n- 3-4 finger syndactyly\n- Feeding difficulties in infancy\n- Duane anomaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Smooth philtrum\n- Long philtrum\n- Low-set ears\n- Broad nasal tip\n- Deeply set eye\n- Atypical behavior\n- Autism\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Ventricular septal defect\n- Coronal craniosynostosis\n- Attention deficit hyperactivity disorder\n- Low hanging columella\n- Pica\n- Upper eyelid edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Dolichocephaly\n- Epicanthus\n- Smooth philtrum\n- Hypoplasia of the maxilla\n- Low-set ears\n- Broad nasal tip\n- Anteverted nares\n- Astigmatism\n- Deeply set eye\n- Hypermetropia\n- Atypical behavior\n- Aggressive behavior\n- Short attention span\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Exaggerated cupid's bow\n- Short nose\n- Depressed nasal bridge\n- Lateral ventricle dilatation\n- Upper eyelid edema\n- Narrow palpebral fissure\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Long philtrum\n- Broad nasal tip\n- Deeply set eye\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Delayed CNS myelination\n- Exaggerated cupid's bow\n- Low hanging columella\n- Upper eyelid edema\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low-set ears\n- Hypermetropia\n- Atypical behavior\n- Psychosis\n- Autism\n- Aggressive behavior\n- Anxiety\n- Delayed speech and language development\n- Nephrolithiasis\n- Osteoporosis\n- Global developmental delay\n- Talipes equinovarus\n- Constipation\n- Cerebral atrophy\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Sleep disturbance\n- Spina bifida occulta\n- Low hanging columella\n- Mild hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Low-set ears\n- Broad nasal tip\n- Deeply set eye\n- Hypermetropia\n- Atypical behavior\n- Delayed speech and language development\n- Global developmental delay\n- Motor delay\n- Sandal gap\n- Constipation\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Sleep disturbance\n- Low hanging columella\n- Sleep apnea\n- Sleep myoclonus\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autism\n- Delayed speech and language development\n- Eczema\n- Global developmental delay\n- Motor delay\n- Intellectual disability, moderate\n- Hypotension\n- Clinodactyly of the 4th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- High palate\n- Broad nasal tip\n- Deeply set eye\n- Atypical behavior\n- Autism\n- Abnormal repetitive mannerisms\n- Self-mutilation\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Cerebral atrophy\n- Ventriculomegaly\n- Sleep disturbance\n- Aphasia\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Periventricular leukomalacia\n- Corneal degeneration\n- Intellectual disability, severe\n- Feeding difficulties\n- Infantile spasms\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Hypoplasia of the maxilla\n- Broad nasal tip\n- Astigmatism\n- Deeply set eye\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Anxiety\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Gastroesophageal reflux\n- Drooling\n- Unsteady gait\n- Intellectual disability, moderate\n- Upper eyelid edema\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Atypical behavior\n- Short attention span\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Intellectual disability, severe\n- Narrow palpebral fissure\n- Arachnoid cyst\n- Lateral ventricular asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Thin upper lip vermilion\n- Smooth philtrum\n- Hypoplasia of the maxilla\n- Long philtrum\n- Posteriorly rotated ears\n- Hearing impairment\n- Low-set ears\n- Broad nasal tip\n- Deeply set eye\n- Atypical behavior\n- Autism\n- Delayed speech and language development\n- Hyperactivity\n- Abnormality of the hand\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Bilateral ptosis\n- Sleep disturbance\n- Clinodactyly of the 5th finger\n- Attention deficit hyperactivity disorder\n- Microtia\n- Low hanging columella\n- Intellectual disability, severe\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Deeply set eye\n- Hypotelorism\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Supernumerary nipple\n- Short nose\n- Depressed nasal bridge\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/09707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Intellectual disability\n- Lymphoma\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/09708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Tall stature\n- Mandibular prognathia\n- Large hands\n- Long foot\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/09709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Bifid uvula\n- Thin upper lip vermilion\n- Epicanthus\n- Smooth philtrum\n- Long philtrum\n- Posteriorly rotated ears\n- Low-set ears\n- Anteverted nares\n- Deeply set eye\n- Esotropia\n- Atypical behavior\n- Autism\n- Abnormal repetitive mannerisms\n- Disinhibition\n- Delayed speech and language development\n- Brachydactyly\n- Tapered finger\n- Global developmental delay\n- Motor delay\n- Plagiocephaly\n- Delayed CNS myelination\n- Exaggerated cupid's bow\n- Polyphagia\n- Short nose\n- Depressed nasal bridge\n- Large earlobe\n- Low hanging columella\n- Intellectual disability, severe\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Atrial septal defect\n- Thromboembolism\n- Hypoglycemia\n- Intractable diarrhea\n- Woolly hair\n- Elevated hepatic transaminase\n- Prominent forehead\n- Villous atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Atrial septal defect\n- Thromboembolism\n- Hypoglycemia\n- Intractable diarrhea\n- Woolly hair\n- Elevated hepatic transaminase\n- Prominent forehead\n- Villous atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Wide nasal bridge\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Atrial septal defect\n- Thromboembolism\n- Hypoglycemia\n- Intractable diarrhea\n- Woolly hair\n- Elevated hepatic transaminase\n- Prominent forehead\n- Villous atrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Telecanthus\n- Nephrolithiasis\n- Failure to thrive\n- Intrauterine growth retardation\n- Abnormal hair morphology\n- Vomiting\n- Intractable diarrhea\n- Woolly hair\n- Decreased circulating IgG level\n- Short stature\n- Decreased body weight\n- Perianal abscess\n- Trichorrhexis nodosa\n- Prominent forehead\n- Bloody diarrhea\n- Pancolitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Broad forehead\n- Low-set ears\n- Skin rash\n- Failure to thrive\n- Growth delay\n- Abnormal hair morphology\n- Weight loss\n- Fever\n- Intractable diarrhea\n- Depressed nasal bridge\n- Recurrent bacterial skin infections\n- Decreased urine output\n- Dry hair\n- Cough\n- Rhinorrhea\n- Skin vesicle\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Cutis laxa\n- Abnormal hair morphology\n- Elevated hepatic transaminase\n- Decreased body weight\n- Secretory diarrhea\n- Sparse hair\n- Trichorrhexis nodosa\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Deeply set eye\n- Atypical behavior\n- Autism\n- Aggressive behavior\n- Delayed speech and language development\n- Global developmental delay\n- Atrial septal defect\n- Exaggerated cupid's bow\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- High palate\n- Epicanthus\n- Smooth philtrum\n- Posteriorly rotated ears\n- Low-set ears\n- Conductive hearing impairment\n- Broad nasal tip\n- Anteverted nares\n- Astigmatism\n- Deeply set eye\n- Myopia\n- Atypical behavior\n- Restlessness\n- Short attention span\n- Low frustration tolerance\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Sparse scalp hair\n- Exaggerated cupid's bow\n- Recurrent infections\n- Short nose\n- Depressed nasal bridge\n- Prominent forehead\n- Upper eyelid edema\n- Abnormal temper tantrums\n- Sparse medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/09718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Amenorrhea\n- Wide nasal bridge\n- Proptosis\n- Osteoporosis\n- Intellectual disability, mild\n- Intrauterine growth retardation\n- Small for gestational age\n- Chronic diarrhea\n- Intractable diarrhea\n- Woolly hair\n- Short stature\n- Decreased body weight\n- Trichorrhexis nodosa\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Amenorrhea\n- Wide nasal bridge\n- Proptosis\n- Osteoporosis\n- Intellectual disability, mild\n- Intrauterine growth retardation\n- Small for gestational age\n- Chronic diarrhea\n- Intractable diarrhea\n- Woolly hair\n- Short stature\n- Decreased body weight\n- Trichorrhexis nodosa\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Global developmental delay\n- Failure to thrive\n- Intrauterine growth retardation\n- Abnormal hair morphology\n- Chronic diarrhea\n- Intractable diarrhea\n- Woolly hair\n- Brittle hair\n- Immunodeficiency\n- Short stature\n- Decreased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Broad forehead\n- Protruding ear\n- Intrauterine growth retardation\n- Hypoglycemia\n- Vomiting\n- Chronic diarrhea\n- Intractable diarrhea\n- Curly hair\n- Abdominal distention\n- Short stature\n- Decreased body weight\n- Hypopigmentation of hair\n- Generalized hypopigmentation\n- Prominent forehead\n- Feeding difficulties\n- Fetal distress\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Hypertelorism\n- Wide nasal bridge\n- Autism\n- Intellectual disability\n- Cirrhosis\n- Failure to thrive\n- Small for gestational age\n- Abnormal hair morphology\n- Intractable diarrhea\n- Pneumonia\n- Woolly hair\n- Hepatomegaly\n- Decreased circulating IgA level\n- Immunodeficiency\n- Elevated hepatic transaminase\n- Decreased circulating IgG level\n- Trichorrhexis nodosa\n- Prominent forehead\n- Bence Jones Proteinuria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Hypertelorism\n- Wide nasal bridge\n- Autism\n- Intellectual disability\n- Cirrhosis\n- Failure to thrive\n- Small for gestational age\n- Abnormal hair morphology\n- Intractable diarrhea\n- Pneumonia\n- Woolly hair\n- Hepatomegaly\n- Decreased circulating IgA level\n- Immunodeficiency\n- Elevated hepatic transaminase\n- Decreased circulating IgG level\n- Trichorrhexis nodosa\n- Prominent forehead\n- Bence Jones Proteinuria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Hypertelorism\n- Broad forehead\n- Wide nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Recurrent otitis media\n- Hyperkeratosis\n- Telangiectasia\n- Poikiloderma\n- Papilledema\n- Growth delay\n- Splenomegaly\n- Frontal bossing\n- Vasculitis\n- Short nose\n- Dermal atrophy\n- Depressed nasal bridge\n- Finger joint hypermobility\n- Recurrent bronchopulmonary infections\n- Telangiectases of the cheeks\n- Reticulated skin pigmentation\n- Plantar hyperkeratosis\n- Palmar hyperkeratosis\n- Midface retrusion\n- Stiff elbow\n- Aplasia\/Hypoplasia of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Facial asymmetry\n- Wide nasal bridge\n- Eczema\n- Hemihypertrophy\n- Recurrent respiratory infections\n- Scoliosis\n- Increased circulating IgE level\n- Onychomycosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Papule\n- Pustule\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Strabismus\n- Myopia\n- Exotropia\n- Nystagmus\n- Albinism\n- Spontaneous, recurrent epistaxis\n- Prolonged bleeding after surgery\n- Hypoplasia of the fovea\n- Impaired ristocetin-induced platelet aggregation\n- Ecchymosis\n- Reduced platelet dense granules\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Menorrhagia\n- Nystagmus\n- Albinism\n- Pulmonary fibrosis\n- Exertional dyspnea\n- Prolonged bleeding time\n- Reduced visual acuity\n- Maculopapular exanthema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Abnormality of the dentition\n- Gingival overgrowth\n- Hypertelorism\n- Smooth philtrum\n- Wide nasal bridge\n- Webbed neck\n- Glaucoma\n- Thick eyebrow\n- Lymphedema\n- Syndactyly\n- Pleural effusion\n- Hypoalbuminemia\n- Preauricular pit\n- Chylothorax\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Nystagmus\n- Albinism\n- Hemolytic anemia\n- Iron deficiency anemia\n- Lower limb pain\n- Abnormal platelet aggregation\n- Ecchymosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Nystagmus\n- Albinism\n- Hemolytic anemia\n- Iron deficiency anemia\n- Lower limb pain\n- Abnormal platelet aggregation\n- Ecchymosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Nystagmus\n- Albinism\n- Hemolytic anemia\n- Iron deficiency anemia\n- Lower limb pain\n- Abnormal platelet aggregation\n- Ecchymosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/09738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Prominent nose\n- Global developmental delay\n- Failure to thrive\n- Neutropenia\n- Pancytopenia\n- Leukopenia\n- Lymphopenia\n- Anemia\n- Chronic diarrhea\n- Pneumonia\n- Chronic oral candidiasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Hypertelorism\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Lymphedema\n- Ascites\n- Hypoproteinemia\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ureteral stenosis\n- Hydronephrosis\n- Narrow mouth\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Abnormal pinna morphology\n- Mixed hearing impairment\n- Thick eyebrow\n- Narrow chest\n- Lymphedema\n- Syndactyly\n- Global developmental delay\n- Neonatal hypotonia\n- Umbilical hernia\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Epicanthus\n- Hypertelorism\n- Abnormal pinna morphology\n- Thick eyebrow\n- Edema\n- Abnormality of skin pigmentation\n- Lymphedema\n- Global developmental delay\n- Small for gestational age\n- Ascites\n- Chronic diarrhea\n- Intestinal lymphangiectasia\n- Short stature\n- Depressed nasal bridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrodontia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/09743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Enlarged kidney\n- Narrow mouth\n- Abnormality of the dentition\n- Gingival overgrowth\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Abnormal pinna morphology\n- Thick eyebrow\n- Narrow chest\n- Lymphedema\n- Spastic diplegia\n- Tremor\n- Hip dysplasia\n- Umbilical hernia\n- Hypoplastic toenails\n- Hypoplasia of the corpus callosum\n- Ventriculomegaly\n- Cerebral cortical atrophy\n- Short stature\n- Depressed nasal bridge\n- Moderate global developmental delay\n- Flat face\n- Myoclonic seizure\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/09747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Horseshoe kidney\n- Gingival overgrowth\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Abnormal pinna morphology\n- Thick eyebrow\n- Narrow chest\n- Lymphedema\n- Global developmental delay\n- Growth delay\n- Ventricular septal defect\n- Short stature\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Moderate global developmental delay\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Edema\n- Intellectual disability\n- Overlapping toe\n- Patchy alopecia\n- Frontal upsweep of hair\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Thoracic scoliosis\n- Hypoalbuminemia\n- Short stature\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Aplasia\/Hypoplasia of the 5th finger\n- Microtia\n- Atonic seizure\n- Flat face\n- Decreased CSF protein concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Edema\n- Intellectual disability\n- Overlapping toe\n- Patchy alopecia\n- Frontal upsweep of hair\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Thoracic scoliosis\n- Hypoalbuminemia\n- Short stature\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Aplasia\/Hypoplasia of the 5th finger\n- Microtia\n- Atonic seizure\n- Flat face\n- Decreased CSF protein concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Edema\n- Intellectual disability\n- Overlapping toe\n- Patchy alopecia\n- Frontal upsweep of hair\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Thoracic scoliosis\n- Hypoalbuminemia\n- Short stature\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Aplasia\/Hypoplasia of the 5th finger\n- Microtia\n- Atonic seizure\n- Flat face\n- Decreased CSF protein concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Edema\n- Intellectual disability\n- Overlapping toe\n- Patchy alopecia\n- Frontal upsweep of hair\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Thoracic scoliosis\n- Hypoalbuminemia\n- Short stature\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Aplasia\/Hypoplasia of the 5th finger\n- Microtia\n- Atonic seizure\n- Flat face\n- Decreased CSF protein concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Edema\n- Intellectual disability\n- Overlapping toe\n- Patchy alopecia\n- Frontal upsweep of hair\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Thoracic scoliosis\n- Hypoalbuminemia\n- Short stature\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Aplasia\/Hypoplasia of the 5th finger\n- Microtia\n- Atonic seizure\n- Flat face\n- Decreased CSF protein concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/09754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/09755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/09756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Micropenis\n- Hypogonadism\n- Microcephaly\n- Epicanthus\n- Low anterior hairline\n- Micrognathia\n- Low-set ears\n- Recurrent otitis media\n- Bulbous nose\n- Downslanted palpebral fissures\n- Anxiety\n- Hyperactivity\n- Gynecomastia\n- Eczema\n- Tapered finger\n- Reduced tendon reflexes\n- Specific learning disability\n- Umbilical hernia\n- High pitched voice\n- Leukopenia\n- Reticulocytosis\n- Truncal obesity\n- Low posterior hairline\n- Premature graying of hair\n- Exertional dyspnea\n- Inverted nipples\n- Acute episodes of neuropathic symptoms\n- Short palm\n- Short stature\n- Increased mean corpuscular volume\n- Bone marrow hypocellularity\n- 2-4 finger syndactyly\n- Persistence of hemoglobin F\n- Panic attack\n- Small, conical teeth\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/09757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/09758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/09759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/09760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/09761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Poikiloderma\n- Hyperextensibility of the finger joints\n- Growth delay\n- Splenomegaly\n- Neutropenia\n- Leukopenia\n- Elevated circulating creatine kinase concentration\n- Sparse lateral eyebrow\n- Nail dystrophy\n- Aplasia\/Hypoplasia of the mandible\n- Midface retrusion\n- Increased circulating lactate dehydrogenase concentration\n- Aplasia\/Hypoplasia of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Long philtrum\n- Poikiloderma\n- Hyperextensibility of the finger joints\n- Growth delay\n- Splenomegaly\n- Neutropenia\n- Leukopenia\n- Elevated circulating creatine kinase concentration\n- Sparse lateral eyebrow\n- Nail dystrophy\n- Aplasia\/Hypoplasia of the mandible\n- Midface retrusion\n- Increased circulating lactate dehydrogenase concentration\n- Aplasia\/Hypoplasia of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Recurrent otitis media\n- Underdeveloped nasal alae\n- Cutaneous photosensitivity\n- Poikiloderma\n- Hyperextensibility of the finger joints\n- Growth delay\n- Neutropenia\n- Leukopenia\n- Low posterior hairline\n- Myelodysplasia\n- Elevated circulating creatine kinase concentration\n- Short stature\n- Sparse lateral eyebrow\n- Recurrent bronchopulmonary infections\n- Recurrent sinusitis\n- Increased circulating lactate dehydrogenase concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microretrognathia\n- Recurrent otitis media\n- Underdeveloped nasal alae\n- Cutaneous photosensitivity\n- Poikiloderma\n- Hyperextensibility of the finger joints\n- Growth delay\n- Neutropenia\n- Leukopenia\n- Low posterior hairline\n- Myelodysplasia\n- Elevated circulating creatine kinase concentration\n- Short stature\n- Sparse lateral eyebrow\n- Recurrent bronchopulmonary infections\n- Recurrent sinusitis\n- Increased circulating lactate dehydrogenase concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Nasolacrimal duct obstruction\n- Carious teeth\n- Palmoplantar keratoderma\n- Cutaneous photosensitivity\n- Atrophic scars\n- Splenomegaly\n- Neutropenia\n- Leukopenia\n- Pulmonary infiltrates\n- Abnormal blistering of the skin\n- Abnormal toenail morphology\n- Folliculitis\n- Polyclonal elevation of circulating IgG\n- Polyclonal elevation of circulating IgA\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Micropenis\n- Hypertelorism\n- Myopia\n- Absent eyelashes\n- Delayed puberty\n- Osteopenia\n- Palmoplantar hyperkeratosis\n- Skin rash\n- Cutaneous photosensitivity\n- Poikiloderma\n- Autoamputation\n- Flexion contracture\n- Onychogryposis\n- Neutropenia\n- Leukopenia\n- Frontal bossing\n- Sparse axillary hair\n- Osteomyelitis\n- Metaphyseal widening\n- Short nose\n- Depressed nasal bridge\n- Sparse lateral eyebrow\n- Sparse facial hair\n- Nail dystrophy\n- Breast hypertrophy\n- Flexion contracture of finger\n- Increased circulating lactate dehydrogenase concentration\n- obsolete Small scrotum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Low anterior hairline\n- Wide nasal bridge\n- Hepatic steatosis\n- Failure to thrive\n- Diarrhea\n- Woolly hair\n- Hepatomegaly\n- Colitis\n- Decreased body weight\n- Trichorrhexis nodosa\n- Abnormal frontal bone morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Intrauterine growth retardation\n- Abnormal hair morphology\n- Diarrhea\n- Intractable diarrhea\n- Recurrent respiratory infections\n- Immunodeficiency\n- Elevated hepatic transaminase\n- Trichorrhexis nodosa\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/09769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed puberty\n- Edema\n- Global developmental delay\n- Intestinal lymphangiectasia\n- Predominantly lower limb lymphedema\n- Pulmonary lymphangiectasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed puberty\n- Edema\n- Global developmental delay\n- Intestinal lymphangiectasia\n- Predominantly lower limb lymphedema\n- Pulmonary lymphangiectasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed puberty\n- Edema\n- Global developmental delay\n- Intestinal lymphangiectasia\n- Predominantly lower limb lymphedema\n- Pulmonary lymphangiectasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed puberty\n- Edema\n- Global developmental delay\n- Intestinal lymphangiectasia\n- Predominantly lower limb lymphedema\n- Pulmonary lymphangiectasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/09773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Long philtrum\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Limb hypertonia\n- Severe T-cell immunodeficiency\n- Focal white matter lesions\n- Abnormal myelination\n- Delayed ability to sit\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/09774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Hypertelorism\n- Micrognathia\n- Prominent nose\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Recurrent respiratory infections\n- Attached earlobe\n- Short palpebral fissure\n- Anteverted ears\n- Thin eyebrow\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/09775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Long philtrum\n- Visual impairment\n- Papilledema\n- Seizure\n- Short nose\n- Flat forehead\n- Coronal craniosynostosis\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/09776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Prominent supraorbital ridges\n- Long philtrum\n- Visual impairment\n- Papilledema\n- Seizure\n- Short nose\n- Flat forehead\n- Coronal craniosynostosis\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/09777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Intellectual disability\n- Seizure\n- Ascites\n- Lymphopenia\n- Patchy alopecia\n- Intestinal lymphangiectasia\n- Hypokalemia\n- Hypocalcemia\n- Hypoalbuminemia\n- Hypoproteinemia\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Pedal edema\n- Flat face\n- Periorbital edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Thickened helices\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Intellectual disability\n- Seizure\n- Lymphopenia\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Hypomagnesemia\n- Hypoalbuminemia\n- Hypoproteinemia\n- Decreased circulating antibody level\n- Low levels of vitamin A\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Microtia\n- Pedal edema\n- Flat face\n- Genital edema\n- Decreased serum zinc\n- Low levels of vitamin E\n- Periorbital edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Thickened helices\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Delayed puberty\n- Intellectual disability\n- Seizure\n- Lymphopenia\n- Intestinal lymphangiectasia\n- Hypocalcemia\n- Hypomagnesemia\n- Hypoalbuminemia\n- Hypoproteinemia\n- Decreased circulating antibody level\n- Low levels of vitamin A\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Microtia\n- Pedal edema\n- Flat face\n- Genital edema\n- Decreased serum zinc\n- Low levels of vitamin E\n- Periorbital edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Intellectual disability\n- Ascites\n- Lymphopenia\n- Intestinal lymphangiectasia\n- Hypoalbuminemia\n- Hypoproteinemia\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Microtia\n- Pedal edema\n- Edema of the upper limbs\n- Flat face\n- Genital edema\n- Low levels of vitamin E\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- High palate\n- Thin upper lip vermilion\n- Retrognathia\n- Epicanthus\n- Hypertelorism\n- Thickened helices\n- Stenosis of the external auditory canal\n- Abnormality of refraction\n- Thick eyebrow\n- Narrow chest\n- Intellectual disability\n- Ascites\n- Lymphopenia\n- Intestinal lymphangiectasia\n- Hypoalbuminemia\n- Hypoproteinemia\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Congenital foot contractures\n- Flexion contracture of toe\n- Microtia\n- Pedal edema\n- Edema of the upper limbs\n- Flat face\n- Genital edema\n- Low levels of vitamin E\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/09782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Recurrent otitis media\n- Carious teeth\n- Palmoplantar keratoderma\n- Cutaneous photosensitivity\n- Poikiloderma\n- Atrophic scars\n- Abnormality of the hand\n- Global developmental delay\n- Hepatosplenomegaly\n- Failure to thrive\n- Growth delay\n- Abnormality of the nail\n- Neutropenia\n- Frontal bossing\n- Recurrent infections\n- Elevated hepatic transaminase\n- Short nose\n- Short stature\n- Acute myelomonocytic leukemia\n- Depressed nasal bridge\n- Recurrent aphthous stomatitis\n- Localized skin lesion\n- Midface retrusion\n- Increased circulating lactate dehydrogenase concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypogonadotropic hypogonadism\n- Micropenis\n- Macrotia\n- Anteverted nares\n- Hypermetropia\n- Thick eyebrow\n- Long palpebral fissure\n- Jaundice\n- Brachydactyly\n- Tapered finger\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Postural instability\n- Thick nasal alae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Poikiloderma\n- Atrophic scars\n- Abnormality of the nail\n- Neutropenia\n- Leukopenia\n- Recurrent infections\n- Recurrent upper respiratory tract infections\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microretrognathia\n- Poikiloderma\n- Atrophic scars\n- Abnormality of the nail\n- Neutropenia\n- Leukopenia\n- Recurrent infections\n- Recurrent upper respiratory tract infections\n- Joint hyperflexibility\n- Finger joint hypermobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Epicanthus\n- Long philtrum\n- Broad nasal tip\n- Anteverted nares\n- Deeply set eye\n- Depression\n- Aggressive behavior\n- Delayed speech and language development\n- Hypothyroidism\n- Tapered finger\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Obesity\n- Sleep disturbance\n- Polyphagia\n- Short nose\n- Thick nasal alae\n- Fatigue\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Epicanthus\n- Long philtrum\n- Broad nasal tip\n- Anteverted nares\n- Deeply set eye\n- Depression\n- Aggressive behavior\n- Delayed speech and language development\n- Hypothyroidism\n- Tapered finger\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Plagiocephaly\n- Obesity\n- Sleep disturbance\n- Polyphagia\n- Short nose\n- Thick nasal alae\n- Fatigue\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Broad nasal tip\n- Anteverted nares\n- Myopia\n- Thick eyebrow\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Constipation\n- Postural instability\n- Short nose\n- Feeding difficulties in infancy\n- Delayed ability to walk\n- Encopresis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Broad nasal tip\n- Anteverted nares\n- Myopia\n- Thick eyebrow\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Constipation\n- Postural instability\n- Short nose\n- Feeding difficulties in infancy\n- Delayed ability to walk\n- Encopresis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Long philtrum\n- Low-set ears\n- Underdeveloped nasal alae\n- Astigmatism\n- Ptosis\n- Myopia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Horizontal nystagmus\n- Macrodontia of permanent maxillary central incisor\n- Jaundice\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypoglycemia\n- Constipation\n- Ventriculomegaly\n- Depressed nasal bridge\n- Pes valgus\n- Esodeviation\n- Delayed ability to walk\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick lower lip vermilion\n- Long philtrum\n- Low-set ears\n- Underdeveloped nasal alae\n- Astigmatism\n- Ptosis\n- Myopia\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Horizontal nystagmus\n- Macrodontia of permanent maxillary central incisor\n- Jaundice\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypoglycemia\n- Constipation\n- Ventriculomegaly\n- Depressed nasal bridge\n- Pes valgus\n- Esodeviation\n- Delayed ability to walk\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Underdeveloped nasal alae\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Aggressive behavior\n- Delayed speech and language development\n- Brachydactyly\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Obesity\n- Sleep disturbance\n- Polyphagia\n- Genu valgum\n- Attention deficit hyperactivity disorder\n- Frequent temper tantrums\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Horseshoe kidney\n- High forehead\n- Broad nasal tip\n- Strabismus\n- Myopia\n- Thick eyebrow\n- Synophrys\n- obsolete Mood swings\n- Anxiety\n- Delayed speech and language development\n- Gynecomastia\n- Tapered finger\n- 2-3 finger syndactyly\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Camptodactyly of toe\n- Postural instability\n- Fatigue\n- Suicidal ideation\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Macrotia\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Thick eyebrow\n- Aggressive behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Obesity\n- Phimosis\n- Pes planus\n- Clinodactyly of the 5th finger\n- Accelerated skeletal maturation\n- High hypermetropia\n- Delayed ability to walk\n- Narrow palpebral fissure\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Short philtrum\n- Macrotia\n- Recurrent otitis media\n- Short neck\n- Deeply set eye\n- Thick eyebrow\n- Synophrys\n- Depression\n- Delayed speech and language development\n- Jaundice\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Obesity\n- Type II diabetes mellitus\n- Feeding difficulties in infancy\n- Thick nasal alae\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Recurrent urinary tract infections\n- Epicanthus\n- Long philtrum\n- Macrotia\n- Wide nasal bridge\n- Anteverted nares\n- Autism\n- Delayed speech and language development\n- 2-3 finger syndactyly\n- Global developmental delay\n- Joint hypermobility\n- Hip dysplasia\n- Constipation\n- Sleep disturbance\n- Short nose\n- Clinodactyly of the 5th finger\n- Attention deficit hyperactivity disorder\n- Speech apraxia\n- Abnormality of coordination\n- Hip subluxation\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Hypotelorism\n- Oligomenorrhea\n- Intellectual disability\n- Global developmental delay\n- Hand tremor\n- Recurrent pneumonia\n- Obsessive-compulsive trait\n- Recurrent sinusitis\n- Delayed menarche\n- Parasomnia\n- Delayed ability to walk\n- Self-injurious behavior\n- Shyness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/09806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dry skin\n- Palmoplantar keratoderma\n- Poikiloderma\n- Global developmental delay\n- Hepatosplenomegaly\n- Hoarse voice\n- Neutropenia\n- Pleural effusion\n- Recurrent infections\n- Respiratory failure\n- Spotty hypopigmentation\n- Infantile axial hypotonia\n- Chronic oral candidiasis\n- Scaling skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrotia\n- Anteverted nares\n- Deeply set eye\n- Thick eyebrow\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Obesity\n- Clumsiness\n- Short nose\n- 2-3 toe syndactyly\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Micrognathia\n- Aggressive behavior\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability\n- Neonatal hypotonia\n- Obesity\n- Short nose\n- Feeding difficulties in infancy\n- Delayed ability to walk\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Gynecomastia\n- 2-3 finger syndactyly\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Obesity\n- Omphalocele\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Macrotia\n- Anteverted nares\n- Strabismus\n- Hypermetropia\n- Thick eyebrow\n- Hyperactivity\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Sandal gap\n- Constipation\n- Dyspnea\n- Attention deficit hyperactivity disorder\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Anteverted nares\n- Thick eyebrow\n- Delayed speech and language development\n- Hyperactivity\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Attention deficit hyperactivity disorder\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Low-set ears\n- Macrotia\n- Anteverted nares\n- Strabismus\n- Ptosis\n- Myopia\n- Jaundice\n- Tapered finger\n- Intellectual disability\n- Obesity\n- Pes cavus\n- Postural instability\n- Sleep disturbance\n- Recurrent infections\n- Thick nasal alae\n- Frequent temper tantrums\n- Self hugging\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Long philtrum\n- High forehead\n- Low-set ears\n- Macrotia\n- Anteverted nares\n- Ptosis\n- Delayed speech and language development\n- Jaundice\n- Tapered finger\n- Intellectual disability\n- Global developmental delay\n- Pes planus\n- Postural instability\n- Sleep disturbance\n- Recurrent infections\n- Attention deficit hyperactivity disorder\n- Thick nasal alae\n- Frequent temper tantrums\n- Delayed ability to walk\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/09814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/09815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/09816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/09817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/09818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/09819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/09820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/09821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Poikiloderma\n- Neutropenia\n- Recurrent infections\n- Cerebral palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Poikiloderma\n- Global developmental delay\n- Neutropenia\n- Hepatomegaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Palmoplantar hyperkeratosis\n- Poikiloderma\n- Global developmental delay\n- Abnormality of the nail\n- Onychogryposis\n- Neutropenia\n- Leukopenia\n- Hepatomegaly\n- Recurrent infections\n- Increased circulating antibody level\n- Calcinosis cutis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Recurrent otitis media\n- Dry skin\n- Eczema\n- Hypopigmented skin patches\n- Hepatosplenomegaly\n- Failure to thrive\n- Leukocytosis\n- Respiratory insufficiency\n- Bronchiectasis\n- Intermittent diarrhea\n- Chronic mucocutaneous candidiasis\n- Short stature\n- Decreased body weight\n- Recurrent pneumonia\n- Absent tonsils\n- Verrucae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the skeletal system\n- Eczema\n- Atopic dermatitis\n- Failure to thrive\n- Eosinophilia\n- Abnormal lung morphology\n- Recurrent bacterial infections\n- Chronic mucocutaneous candidiasis\n- Recurrent bronchitis\n- Increased circulating IgE level\n- Severe T-cell immunodeficiency\n- Cough\n- Pulmonary pneumatocele\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the skeletal system\n- Eczema\n- Atopic dermatitis\n- Failure to thrive\n- Eosinophilia\n- Abnormal lung morphology\n- Recurrent bacterial infections\n- Chronic mucocutaneous candidiasis\n- Recurrent bronchitis\n- Increased circulating IgE level\n- Severe T-cell immunodeficiency\n- Cough\n- Pulmonary pneumatocele\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the skeletal system\n- Eczema\n- Atopic dermatitis\n- Failure to thrive\n- Eosinophilia\n- Abnormal lung morphology\n- Recurrent bacterial infections\n- Chronic mucocutaneous candidiasis\n- Recurrent bronchitis\n- Increased circulating IgE level\n- Severe T-cell immunodeficiency\n- Cough\n- Pulmonary pneumatocele\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Underdeveloped nasal alae\n- Delayed speech and language development\n- Melanocytic nevus\n- Intellectual disability\n- Ectropion of lower eyelids\n- Esodeviation\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/09834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Underdeveloped nasal alae\n- Delayed speech and language development\n- Melanocytic nevus\n- Intellectual disability\n- Ectropion of lower eyelids\n- Esodeviation\n- Mild microcephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/09835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/09839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/09840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Open mouth\n- High palate\n- Thin vermilion border\n- Prominent occiput\n- Microretrognathia\n- Long philtrum\n- Micrognathia\n- High forehead\n- Low-set, posteriorly rotated ears\n- Abnormal pinna morphology\n- Wide nasal bridge\n- Short neck\n- Abnormality of the periorbital region\n- Single transverse palmar crease\n- Thin skin\n- Syndactyly\n- Hypertonia\n- Limitation of joint mobility\n- Respiratory distress\n- Short nose\n- Clinodactyly of the 5th finger\n- Sparse hair\n- Microtia\n- Localized skin lesion\n- Flat face\n- Flexion contracture of finger\n- Narrow palpebral fissure\n- Scleroderma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Proptosis\n- Band keratopathy\n- Dental malocclusion\n- Vascular dilatation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Proptosis\n- Dental malocclusion\n- Partial agenesis of the corpus callosum\n- Vertical orbital dystopia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Dental malocclusion\n- Absent frontal sinuses\n- Abnormal foramen magnum morphology\n- Supernumerary tooth\n- Cognitive impairment\n- obsolete Cleft maxillary alveolus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dyspnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dyspnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dyspnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydrocephalus\n- Global developmental delay\n- Coronal craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Proptosis\n- Dental malocclusion\n- Sleep apnea\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Proptosis\n- Craniosynostosis\n- Anterior open-bite malocclusion\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/09854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/09855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/09856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Proptosis\n- Amblyopia\n- Anterior open-bite malocclusion\n- Midface retrusion\n- Lagophthalmos\n- Cross bite\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Proptosis\n- Amblyopia\n- Anterior open-bite malocclusion\n- Midface retrusion\n- Lagophthalmos\n- Cross bite\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Midface retrusion\n- obsolete Bilateral external ear deformity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Proptosis\n- Dental malocclusion\n- Sleep apnea\n- Unicoronal synostosis\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Proptosis\n- Dental malocclusion\n- Sleep apnea\n- Bicoronal synostosis\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/09861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypertelorism\n- Hearing impairment\n- Recurrent otitis media\n- Hyperkeratosis\n- Poikiloderma\n- Joint hypermobility\n- Joint stiffness\n- Splenomegaly\n- Neutropenia\n- Leukopenia\n- Lymphopenia\n- Frontal bossing\n- Short nose\n- Short stature\n- Decreased body weight\n- Dermal atrophy\n- Depressed nasal bridge\n- Midface retrusion\n- Aplasia\/Hypoplasia of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Poikiloderma\n- Splenomegaly\n- Neutropenia\n- Leukopenia\n- Lymphopenia\n- Short stature\n- Nail dystrophy\n- Midface retrusion\n- Aplasia\/Hypoplasia of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microretrognathia\n- Underdeveloped nasal alae\n- Cataract\n- Poikiloderma\n- Neutropenia\n- Leukopenia\n- Low posterior hairline\n- Short stature\n- Sparse lateral eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/09864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow mouth\n- Cleft palate\n- Thin upper lip vermilion\n- Malar flattening\n- Low anterior hairline\n- Bulbous nose\n- Underdeveloped nasal alae\n- Emotional lability\n- Agitation\n- Irritability\n- Hypoplasia of the thymus\n- Hypernasal speech\n- Thrombocytopenia\n- Basal ganglia calcification\n- Hypocalcemia\n- Depressed nasal bridge\n- Enamel hypoplasia\n- Auditory hallucinations\n- Palpebral thickening\n- Insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/09865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Small earlobe\n- Deeply set eye\n- Ptosis\n- Intellectual disability\n- Generalized hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/09871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Retrognathia\n- Low-set ears\n- Ptosis\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Recurrent infections\n- Subglottic laryngitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Preauricular skin tag\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Wide nasal bridge\n- Strabismus\n- Hypermetropia\n- Blepharophimosis\n- Specific learning disability\n- Ventricular septal defect\n- Recurrent infections\n- Bilateral choanal atresia\n- Hypoplasia of the iris\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Ventricular septal defect\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Inverted nipples\n- Wide intermamillary distance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Low-set ears\n- Depressed nasal tip\n- Blepharophimosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Malar flattening\n- Hypertelorism\n- Low-set ears\n- Wide nasal bridge\n- Broad nasal tip\n- Narrow naris\n- Palpebral edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/09879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/09880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/09881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/09882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/09883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/09887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/09888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hearing impairment\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/09889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydronephrosis\n- Sacral dimple\n- Global developmental delay\n- Small for gestational age\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Edema of the dorsum of hands\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/09916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydronephrosis\n- Sacral dimple\n- Global developmental delay\n- Small for gestational age\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Edema of the dorsum of hands\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/09917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hydronephrosis\n- Sacral dimple\n- Global developmental delay\n- Small for gestational age\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Edema of the dorsum of hands\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/09918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Otitis media\n- Eczema\n- Allergy\n- Molluscum contagiosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/09924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Nevus flammeus\n- Umbilical hernia\n- Hypoglycemia\n- Neuroblastoma\n- Anterior creases of earlobe\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hemangioma\n- Nevus flammeus\n- Camptodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Enlarged kidney\n- Macroglossia\n- Hemihypertrophy\n- Dysphagia\n- Hepatomegaly\n- Drooling\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Enlarged kidney\n- Macroglossia\n- Hemihypertrophy\n- Dysphagia\n- Hepatomegaly\n- Drooling\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Hydrocephalus\n- Macrocephaly\n- Papilledema\n- Hemihypertrophy\n- Omphalocele\n- Ventriculomegaly\n- Chiari malformation\n- Bilateral cryptorchidism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/09949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Enlarged kidney\n- Macroglossia\n- Hemangioma\n- Omphalocele\n- Patent foramen ovale\n- Vomiting\n- Abdominal distention\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability, mild\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/09952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Mandibular prognathia\n- Smooth philtrum\n- Broad forehead\n- Long philtrum\n- Bulbous nose\n- Dental crowding\n- Poor wound healing\n- Brachydactyly\n- Intellectual disability, mild\n- Dysmetria\n- Joint hypermobility\n- Obesity\n- Malignant hyperthermia\n- Dysdiadochokinesis\n- Short stature\n- Sparse lateral eyebrow\n- Sparse hair\n- Anterior open-bite malocclusion\n- Radial deviation of the 3rd finger\n- Ulnar deviation of the 3rd finger\n- Ulnar deviation of the 2nd finger\n- Supernumerary tooth\n- Thick vermilion border\n- Flexion contracture of finger\n- Clinodactyly\n- Radial deviation of the 5th finger\n- Cross bite\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Triangular face\n- Broad forehead\n- Bulbous nose\n- Deeply set eye\n- Sparse eyelashes\n- Brachydactyly\n- Thin nail\n- Delayed skeletal maturation\n- Irregular ossification of hand bones\n- Short stature\n- Temporal hypotrichosis\n- Sparse lateral eyebrow\n- Sparse hair\n- Exercise-induced muscle fatigue\n- Ulnar deviation of finger\n- Supernumerary tooth\n- Fatigue\n- Hip pain\n- Sparse eyebrow\n- Synovitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachydactyly\n- Short stature\n- Sparse hair\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Low-set ears\n- Protruding ear\n- Bulbous nose\n- Blue irides\n- Alopecia\n- Broad nail\n- Flat capital femoral epiphysis\n- Sparse lateral eyebrow\n- Anhidrotic ectodermal dysplasia\n- Sparse hair\n- Short phalanx of finger\n- Short metacarpal\n- Small epiphyses of the distal phalanges of the hand\n- Cone-shaped epiphysis\n- Chin with horizontal crease\n- Wrist pain\n- Hip pain\n- Hand pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Low-set ears\n- Protruding ear\n- Bulbous nose\n- Blue irides\n- Alopecia\n- Broad nail\n- Flat capital femoral epiphysis\n- Sparse lateral eyebrow\n- Anhidrotic ectodermal dysplasia\n- Sparse hair\n- Short phalanx of finger\n- Short metacarpal\n- Small epiphyses of the distal phalanges of the hand\n- Cone-shaped epiphysis\n- Chin with horizontal crease\n- Wrist pain\n- Hip pain\n- Hand pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Coarse facial features\n- Aggressive behavior\n- Abnormal repetitive mannerisms\n- Seizure\n- Global developmental delay\n- Growth delay\n- Pulmonic stenosis\n- Abnormal facial shape\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/09958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/09959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/09960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/09961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Butterfly vertebrae\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/09962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/09964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/09965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/09966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Broad forehead\n- Anxiety\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cupped ear\n- Protruding ear\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Broad forehead\n- Protruding ear\n- Joint hypermobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Broad forehead\n- Protruding ear\n- Joint hypermobility\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Broad forehead\n- Protruding ear\n- Joint hypermobility\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Broad forehead\n- Protruding ear\n- Joint hypermobility\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Triangular face\n- Long philtrum\n- Micrognathia\n- Macrotia\n- Protruding ear\n- Bulbous nose\n- Sparse eyelashes\n- Joint hypermobility\n- Growth delay\n- Pes planus\n- Fragile nails\n- Clinodactyly of the 5th toe\n- Fine hair\n- Fair hair\n- Delayed skeletal maturation\n- Short stature\n- Sparse lateral eyebrow\n- Sparse hair\n- Cone-shaped epiphysis\n- Prominent forehead\n- Mild global developmental delay\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Triangular face\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Sparse eyelashes\n- Fragile nails\n- Clinodactyly of the 5th toe\n- Hyperlordosis\n- Clinodactyly of the 5th finger\n- Short stature\n- Sparse lateral eyebrow\n- Sparse hair\n- Prominent forehead\n- Endometriosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Triangular face\n- Long philtrum\n- Micrognathia\n- Protruding ear\n- Bulbous nose\n- Sparse eyelashes\n- Sparse lateral eyebrow\n- Sparse hair\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Triangular face\n- Long philtrum\n- Micrognathia\n- Protruding ear\n- Bulbous nose\n- Sparse eyelashes\n- Sparse lateral eyebrow\n- Sparse hair\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/09978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Mandibular prognathia\n- Carious teeth\n- Dental malocclusion\n- Nevus flammeus\n- Omphalocele\n- Neonatal hypoglycemia\n- Hepatomegaly\n- Drooling\n- Anterior open-bite malocclusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09979.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Micrognathia\n- Short neck\n- Umbilical hernia\n- Anterior creases of earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/09980.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09981.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09982.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09983.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09984.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09985.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09986.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09987.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09988.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09989.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/09990.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Pointed chin\n- Protruding ear\n- Strabismus\n- Autistic behavior\n- Abnormally large globe\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/09991.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Underdeveloped nasal alae\n- Broad nasal tip\n- Low hanging columella\n- Medial flaring of the eyebrow\n- Broad columella\n- Wide nasal ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09992.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Macrotia\n- Broad nasal tip\n- Fine hair\n- Sparse lateral eyebrow\n- Sparse hair\n- Prominent ear helix\n- Broad columella\n- Sparse medial eyebrow\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09993.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hydrocephalus\n- Macrocephaly\n- Long philtrum\n- Abnormal pinna morphology\n- Macrotia\n- Bulbous nose\n- Brachydactyly\n- Sparse scalp hair\n- Chiari malformation\n- Bowing of the legs\n- Aplasia\/Hypoplasia of the nails\n- Scaphocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09994.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hydrocephalus\n- Macrocephaly\n- Long philtrum\n- Abnormal pinna morphology\n- Macrotia\n- Bulbous nose\n- Brachydactyly\n- Sparse scalp hair\n- Chiari malformation\n- Bowing of the legs\n- Aplasia\/Hypoplasia of the nails\n- Scaphocephaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09995.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Bulbous nose\n- Brachydactyly\n- Growth delay\n- Slow-growing hair\n- Spondylolysis\n- Short stature\n- Sparse lateral eyebrow\n- Sparse hair\n- Deviation of the 2nd finger\n- Abnormality of the temporomandibular joint\n- Clinodactyly\n- Elongated femoral neck\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09996.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Seizure\n- Global developmental delay\n- Cerebellar hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/09997.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Broad nasal tip\n- Thick eyebrow\n- Brachydactyly\n- Growth delay\n- Fine hair\n- Sparse hair\n- Cone-shaped epiphysis\n- Premature epimetaphyseal fusion\n- Broad columella\n- Broad eyebrow\n- Wide nasal ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09998.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Short neck\n- Jaundice\n- Brachydactyly\n- Intellectual disability, mild\n- Global developmental delay\n- Fine hair\n- Hepatomegaly\n- Fair hair\n- Scoliosis\n- Elevated hepatic transaminase\n- Short stature\n- Sparse hair\n- Broad eyebrow\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/09999.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Retrognathia\n- Pectus carinatum\n- Hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/10000.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Ataxia\n- Gait ataxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/10001.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Global developmental delay\n- Fine hair\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10002.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Hyperextensible skin\n- Striae distensae\n- Dilated cardiomyopathy\n- High, narrow palate\n- Intellectual disability, borderline\n- Patellar subluxation\n- Joint subluxation\n- Peritoneal mesothelioma\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/10003.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of visual evoked potentials\n- Autism\n- Delayed speech and language development\n- Ataxia\n- Gait disturbance\n- Slurred speech\n- Fragile nails\n- Aplasia\/Hypoplasia of the cerebellum\n- Distal joint laxity\n- obsolete Psychomotor retardation\n- Cerebral palsy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/10004.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Underdeveloped nasal alae\n- Thick eyebrow\n- Ulnar deviation of the hand or of fingers of the hand\n- Foot oligodactyly\n- Nail dysplasia\n- Multiple exostoses\n- Short stature\n- Shortening of all metacarpals\n- Unilateral ptosis\n- Sparse hair\n- Radial deviation of the hand or of fingers of the hand\n- Thick nasal septum\n- Cone-shaped epiphysis\n- Intellectual disability, severe\n- Absent hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10005.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Underdeveloped nasal alae\n- Brachydactyly\n- Slow-growing hair\n- Shortening of all metacarpals\n- Sparse hair\n- Cone-shaped epiphysis\n- Broad eyebrow\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10006.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10007.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10008.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10009.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10010.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10011.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10012.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Low-set ears\n- Protruding ear\n- Ptosis\n- Long eyelashes\n- Hypermetropia\n- Nystagmus\n- Amblyopia\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Encephalopathy\n- Absent speech\n- Joint hypermobility\n- Abnormal facial shape\n- Constipation\n- Postural instability\n- Generalized-onset seizure\n- EEG abnormality\n- Expressive language delay\n- Excessive salivation\n- Abnormal muscle tone\n- Pes valgus\n- Spasmus nutans\n- Abnormality of pain sensation\n- Abnormality of the pineal gland\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10013.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hearing impairment\n- Low-set ears\n- Ptosis\n- Long eyelashes\n- Autism\n- Delayed speech and language development\n- Abnormal fingernail morphology\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Global developmental delay\n- EEG abnormality\n- Sleep disturbance\n- Aphasia\n- High, narrow palate\n- Elevated circulating alkaline phosphatase concentration\n- Craniofacial disproportion\n- Bilateral conductive hearing impairment\n- Neurodevelopmental delay\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10014.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Facial asymmetry\n- Broad forehead\n- Wide nasal bridge\n- Tapered finger\n- Hypotonia\n- Motor delay\n- Failure to thrive\n- Short toe\n- Abnormal facial shape\n- Moderate hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10015.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Macrocephaly\n- Hypertelorism\n- Facial asymmetry\n- Broad forehead\n- Wide nasal bridge\n- Tapered finger\n- Hypotonia\n- Motor delay\n- Failure to thrive\n- Short toe\n- Abnormal facial shape\n- Moderate hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10016.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Narrow nasal ridge\n- Epistaxis\n- Autism\n- Anxiety\n- Delayed speech and language development\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Selective tooth agenesis\n- Delayed gross motor development\n- Sleep disturbance\n- Abnormal muscle tone\n- Delayed fine motor development\n- Oral cavity bleeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/10017.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Narrow nasal ridge\n- Epistaxis\n- Autism\n- Anxiety\n- Delayed speech and language development\n- Prominent fingertip pads\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Selective tooth agenesis\n- Delayed gross motor development\n- Sleep disturbance\n- Abnormal muscle tone\n- Delayed fine motor development\n- Oral cavity bleeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/10018.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10019.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10020.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10021.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial asymmetry\n- Hepatoblastoma\n- Postauricular pit\n- Lower limb asymmetry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10022.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Umbilical hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10023.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Umbilical hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10024.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thick lower lip vermilion\n- Thick upper lip vermilion\n- Malar flattening\n- Broad forehead\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Anxiety\n- Osteoporosis\n- Intellectual disability\n- Global developmental delay\n- Mitral valve prolapse\n- Coarctation of aorta\n- Short nose\n- Proportionate short stature\n- Supravalvular aortic stenosis\n- Type II diabetes mellitus\n- Attention deficit hyperactivity disorder\n- Stellate iris\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10025.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10026.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10027.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Facial hemangioma\n- Hemifacial hypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10028.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Protruding ear\n- Nevus flammeus\n- Umbilical hernia\n- Diastasis recti\n- Neonatal hypoglycemia\n- Visceromegaly\n- Preauricular pit\n- Hyperechogenic kidneys\n- Increased placental thickness\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10029.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Protruding ear\n- Nevus flammeus\n- Umbilical hernia\n- Diastasis recti\n- Neonatal hypoglycemia\n- Visceromegaly\n- Preauricular pit\n- Hyperechogenic kidneys\n- Increased placental thickness\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10030.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Protruding ear\n- Nevus flammeus\n- Umbilical hernia\n- Diastasis recti\n- Neonatal hypoglycemia\n- Visceromegaly\n- Preauricular pit\n- Hyperechogenic kidneys\n- Increased placental thickness\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10031.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hydronephrosis\n- Macroglossia\n- Umbilical hernia\n- Diastasis recti\n- Hepatomegaly\n- Preauricular pit\n- Anterior creases of earlobe\n- Protruding tongue\n- Infra-orbital crease\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10032.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Enlarged kidney\n- Macroglossia\n- Large for gestational age\n- Umbilical hernia\n- Neonatal hypoglycemia\n- Hemifacial hypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10033.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Abnormality of the kidney\n- Hemangioma\n- Nevus flammeus\n- Large for gestational age\n- Omphalocele\n- Ventricular septal defect\n- Hypoglycemia\n- Hemifacial hypertrophy\n- Abdominal wall defect\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10034.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Enlarged kidney\n- Macroglossia\n- Large for gestational age\n- Omphalocele\n- Constipation\n- Gastroesophageal reflux\n- Nephrogenic rest\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10035.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Enlarged kidney\n- Macroglossia\n- Coarse facial features\n- Large for gestational age\n- Hypertrophic cardiomyopathy\n- Pulmonic stenosis\n- Patent ductus arteriosus\n- Hypoplastic toenails\n- Hypoglycemia\n- Cerebral atrophy\n- Hepatomegaly\n- Tracheobronchomalacia\n- Respiratory failure\n- Abdominal distention\n- Hemifacial hypertrophy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10036.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Postaxial hand polydactyly\n- Seizure\n- Global developmental delay\n- Abnormal corpus callosum morphology\n- Macrodontia\n- Atrial septal defect\n- Keloids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10037.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Renal dysplasia\n- Mandibular prognathia\n- Pointed chin\n- Hypertelorism\n- Wide nasal bridge\n- Broad nasal tip\n- Strabismus\n- Widely spaced teeth\n- Autism\n- Aggressive behavior\n- Delayed speech and language development\n- Reduced eye contact\n- Hemangioma\n- Global developmental delay\n- Umbilical hernia\n- Atrial septal defect\n- Splenomegaly\n- Hypoglycemia\n- Respiratory distress\n- Depressed nasal bridge\n- Elevated circulating alpha-fetoprotein concentration\n- Lower limb asymmetry\n- Upper limb asymmetry\n- Cyst of the ductus choledochus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10038.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/10039.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Juvenile cataract\n- Mitral valve prolapse\n- Poor suck\n- Intellectual disability, moderate\n- High, narrow palate\n- Kyphoscoliosis\n- Postlingual sensorineural hearing impairment\n- Bilateral cryptorchidism\n- Infantile axial hypotonia\n- High myopia\n- Increased arm span\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10040.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Juvenile cataract\n- Mitral valve prolapse\n- Poor suck\n- Intellectual disability, moderate\n- High, narrow palate\n- Kyphoscoliosis\n- Postlingual sensorineural hearing impairment\n- Bilateral cryptorchidism\n- Infantile axial hypotonia\n- High myopia\n- Increased arm span\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10041.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Juvenile cataract\n- Mitral valve prolapse\n- Poor suck\n- Intellectual disability, moderate\n- High, narrow palate\n- Kyphoscoliosis\n- Postlingual sensorineural hearing impairment\n- Bilateral cryptorchidism\n- Infantile axial hypotonia\n- High myopia\n- Increased arm span\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10042.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- High forehead\n- Impaired social interactions\n- Numerous nevi\n- Global developmental delay\n- Scoliosis\n- Macrocephaly at birth\n- Intellectual disability, borderline\n- Proportionate tall stature\n- Dilation of Virchow-Robin spaces\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/10043.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Macrocephaly\n- High forehead\n- Impaired social interactions\n- Numerous nevi\n- Global developmental delay\n- Scoliosis\n- Macrocephaly at birth\n- Intellectual disability, borderline\n- Proportionate tall stature\n- Dilation of Virchow-Robin spaces\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/10044.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Short stature\n- Euryblepharon\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10045.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Seizure\n- Facial palsy\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/10046.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Shawl scrotum\n- Macroglossia\n- Cleft palate\n- Widely spaced teeth\n- Cafe-au-lait spot\n- Intellectual disability\n- Nephroblastoma\n- Exodeviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10047.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microcephaly\n- Global developmental delay\n- Craniosynostosis\n- Short stature\n- Wide nasal base\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/10048.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Open mouth\n- Brachycephaly\n- Hypertelorism\n- Flared nostrils\n- Depressed nasal ridge\n- Proptosis\n- Abnormal skull morphology\n- Cafe-au-lait spot\n- Hemangioma\n- Keratoconjunctivitis sicca\n- Global developmental delay\n- Gastroesophageal reflux\n- Prominent metopic ridge\n- Prolonged neonatal jaundice\n- Underdeveloped supraorbital ridges\n- Ridged cranial sutures\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10049.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow palate\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Overfolded helix\n- Bulbous nose\n- Underdeveloped nasal alae\n- Prominent nose\n- Carious teeth\n- Dental crowding\n- Dental malocclusion\n- Microdontia\n- Dry skin\n- Joint hypermobility\n- Fine hair\n- Fair hair\n- Short palm\n- Sparse lateral eyebrow\n- Shortening of all metacarpals\n- Swelling of proximal interphalangeal joints\n- Sparse hair\n- Cone-shaped epiphysis\n- Chin with horizontal crease\n- Shortening of all phalanges of fingers\n- Anteverted ears\n- Thin eyebrow\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10050.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow palate\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Underdeveloped nasal alae\n- Prominent nose\n- Strabismus\n- Carious teeth\n- Microdontia\n- Hypothyroidism\n- Rib exostoses\n- Scapular exostoses\n- Dry skin\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Joint hypermobility\n- Premature birth\n- Pes planus\n- Short foot\n- Fragile nails\n- Thin nail\n- Fair hair\n- Diffuse cerebral atrophy\n- Scoliosis\n- Multiple exostoses\n- Arthralgia\n- Short palm\n- Sparse lateral eyebrow\n- Shortening of all metacarpals\n- Thyroid hypoplasia\n- Swelling of proximal interphalangeal joints\n- Sparse hair\n- Cone-shaped epiphysis\n- Short metatarsal\n- Chin with horizontal crease\n- Shortening of all phalanges of fingers\n- Mild hearing impairment\n- Abnormal growth hormone level\n- Anteverted ears\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10051.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow palate\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Underdeveloped nasal alae\n- Anteverted nares\n- Myopia\n- Synophrys\n- Carious teeth\n- Dental crowding\n- Dental malocclusion\n- Rib exostoses\n- Scapular exostoses\n- Dry skin\n- Joint hypermobility\n- Ventricular septal defect\n- Atrial septal defect\n- Pulmonic stenosis\n- Short foot\n- Fragile nails\n- Thin nail\n- Scoliosis\n- Recurrent fractures\n- Multiple exostoses\n- Short nose\n- Hyperlordosis\n- Scapular winging\n- Short palm\n- Shortening of all metacarpals\n- Swelling of proximal interphalangeal joints\n- Cerebral hamartoma\n- Prominent ear helix\n- Cone-shaped epiphysis\n- Short metatarsal\n- Chin with horizontal crease\n- Shortening of all phalanges of fingers\n- Low femoral bone density\n- Anteverted ears\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10052.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Narrow palate\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Underdeveloped nasal alae\n- Prominent nose\n- Carious teeth\n- Dental malocclusion\n- Microdontia\n- Rib exostoses\n- Dry skin\n- Hip dysplasia\n- Short foot\n- Fragile nails\n- Thin nail\n- Fine hair\n- Scoliosis\n- Osteoarthritis\n- Multiple exostoses\n- Arthralgia\n- Short palm\n- Reduced bone mineral density\n- Shortening of all metacarpals\n- Swelling of proximal interphalangeal joints\n- Sparse hair\n- Prominent ear helix\n- Cone-shaped epiphysis\n- Short metatarsal\n- Chin with horizontal crease\n- Shortening of all phalanges of fingers\n- Anteverted ears\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10053.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Underdeveloped nasal alae\n- Prominent nose\n- Carious teeth\n- Dental malocclusion\n- Microdontia\n- Dry skin\n- Short foot\n- Fragile nails\n- Thin nail\n- Fine hair\n- Scoliosis\n- Short palm\n- Sparse lateral eyebrow\n- Shortening of all metacarpals\n- Swelling of proximal interphalangeal joints\n- Sparse hair\n- Cone-shaped epiphysis\n- Short metatarsal\n- Shortening of all phalanges of fingers\n- Mild hearing impairment\n- Anteverted ears\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10054.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Nephrocalcinosis\n- Narrow palate\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Underdeveloped nasal alae\n- Prominent nose\n- Carious teeth\n- Dental crowding\n- Dental malocclusion\n- Dry skin\n- Intellectual disability, mild\n- Bicuspid aortic valve\n- Pes planus\n- Short foot\n- Fragile nails\n- Thin nail\n- Coxa magna\n- Short palm\n- Sparse lateral eyebrow\n- Swelling of proximal interphalangeal joints\n- Sparse hair\n- Prominent ear helix\n- Cone-shaped epiphysis\n- Short metatarsal\n- Chin with horizontal crease\n- Shortening of all phalanges of fingers\n- Mild hearing impairment\n- Postterm pregnancy\n- Abnormal growth hormone level\n- Anteverted ears\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10055.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Underdeveloped nasal alae\n- Prominent nose\n- Carious teeth\n- Dental malocclusion\n- Dry skin\n- Pes planus\n- Short foot\n- Thin nail\n- Short palm\n- Sparse lateral eyebrow\n- Shortening of all metacarpals\n- Swelling of proximal interphalangeal joints\n- Sparse hair\n- Cone-shaped epiphysis\n- Short metatarsal\n- Shortening of all phalanges of fingers\n- Anteverted ears\n- Menometrorrhagia\n- Broad medial eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10056.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Protruding ear\n- Pear-shaped nose\n- Brachydactyly\n- Hip dysplasia\n- Sparse axillary hair\n- Slow-growing hair\n- Sparse pubic hair\n- Osteoarthritis\n- Short stature\n- Sparse lateral eyebrow\n- Avascular necrosis of the capital femoral epiphysis\n- Sparse hair\n- Abnormality of the hairline\n- Cone-shaped epiphysis\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10057.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Pear-shaped nose\n- Abnormality of the frontal hairline\n- Alopecia\n- Fragile nails\n- Sparse scalp hair\n- Sparse axillary hair\n- Scoliosis\n- Sparse lateral eyebrow\n- Finger joint hypermobility\n- Swelling of proximal interphalangeal joints\n- Radial deviation of the 4th finger\n- Cone-shaped epiphysis\n- Enlarged epiphyses\n- Radial deviation of the 5th finger\n- Slow-growing scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10058.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Pear-shaped nose\n- Broad nasal tip\n- Brachydactyly\n- Fine hair\n- Deviation of finger\n- Prominent nasal tip\n- Sparse lateral eyebrow\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10059.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hepatic failure\n- Conjugated hyperbilirubinemia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10060.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dental crowding\n- Dental malocclusion\n- Brachydactyly\n- Alopecia\n- Sparse scalp hair\n- Fine hair\n- Sparse axillary hair\n- Sparse body hair\n- Disproportionate short stature\n- Congenital giant melanocytic nevus\n- Short mandibular condyles\n- Brachytelomesophalangy\n- Supernumerary maxillary incisor\n- Slow-growing nails\n- Cone-shaped epiphysis\n- Short metatarsal\n- Open bite\n- Midface retrusion\n- Slow-growing scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10061.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dental crowding\n- Dental malocclusion\n- Brachydactyly\n- Alopecia\n- Sparse scalp hair\n- Fine hair\n- Sparse axillary hair\n- Sparse body hair\n- Disproportionate short stature\n- Congenital giant melanocytic nevus\n- Short mandibular condyles\n- Brachytelomesophalangy\n- Supernumerary maxillary incisor\n- Slow-growing nails\n- Cone-shaped epiphysis\n- Short metatarsal\n- Open bite\n- Midface retrusion\n- Slow-growing scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10062.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Triangular face\n- Long philtrum\n- Micrognathia\n- Protruding ear\n- Bulbous nose\n- Pear-shaped nose\n- Pes planus\n- Brittle hair\n- Deviation of finger\n- Short palm\n- Short stature\n- Temporal hypotrichosis\n- Sparse lateral eyebrow\n- Sparse hair\n- Short finger\n- Short metacarpal\n- Cone-shaped epiphysis\n- Chin with horizontal crease\n- Slow-growing scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10063.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Triangular face\n- Long philtrum\n- Micrognathia\n- Protruding ear\n- Bulbous nose\n- Pear-shaped nose\n- Pes planus\n- Brittle hair\n- Deviation of finger\n- Short palm\n- Short stature\n- Sparse lateral eyebrow\n- Sparse hair\n- Short metacarpal\n- Cone-shaped epiphysis\n- Chin with horizontal crease\n- Slow-growing scalp hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10064.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Pear-shaped nose\n- Carious teeth\n- Brachydactyly\n- Alopecia of scalp\n- Short stature\n- Sparse lateral eyebrow\n- Soft tissue swelling of interphalangeal joints\n- Radial deviation of the 3rd finger\n- Radial deviation of the 2nd finger\n- Cone-shaped epiphysis\n- Supernumerary tooth\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10065.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Smooth philtrum\n- Long philtrum\n- Bulbous nose\n- Dental crowding\n- Failure to thrive\n- Gastroesophageal reflux\n- Sparse scalp hair\n- High, narrow palate\n- Short stature\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10066.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10067.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10068.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the forehead\n- Hypertelorism\n- Convex nasal ridge\n- Proptosis\n- Hyperpigmentation of the skin\n- Acanthosis nigricans\n- Ventriculomegaly\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10069.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10070.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10071.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Retrognathia\n- Underdeveloped nasal alae\n- Wide nose\n- Broad nasal tip\n- Strabismus\n- Downslanted palpebral fissures\n- Anxiety\n- Delayed speech and language development\n- Abnormal posterior cranial fossa morphology\n- Global developmental delay\n- Joint hypermobility\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Scoliosis\n- Cerebellar vermis atrophy\n- Abnormal 2nd metacarpal morphology\n- Persistence of hemoglobin F\n- Abnormal eating behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10072.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Epicanthus\n- Micrognathia\n- Abnormality of the outer ear\n- Prominent nasal bridge\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Broad nasal tip\n- Strabismus\n- Delayed speech and language development\n- Pectus excavatum\n- Ataxia\n- Joint hypermobility\n- Hypoplasia of the corpus callosum\n- Broad-based gait\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Midface retrusion\n- Persistence of hemoglobin F\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10073.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Malar flattening\n- Pointed chin\n- Abnormality of the outer ear\n- Strabismus\n- Downslanted palpebral fissures\n- Blue sclerae\n- Aggressive behavior\n- Delayed speech and language development\n- Abnormal posterior cranial fossa morphology\n- Hypotonia\n- Joint hypermobility\n- Constipation\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Sleep disturbance\n- Abnormal brainstem morphology\n- Repetitive compulsive behavior\n- Maternal diabetes\n- Delayed fine motor development\n- Midface retrusion\n- Recurrent hand flapping\n- Preeclampsia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10074.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Malar flattening\n- Epicanthus\n- Microretrognathia\n- Abnormality of the outer ear\n- Strabismus\n- Delayed speech and language development\n- Seizure\n- Delayed gross motor development\n- Sleep disturbance\n- Intellectual disability, severe\n- Midface retrusion\n- Persistence of hemoglobin F\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10075.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Epicanthus\n- Abnormality of the outer ear\n- Strabismus\n- Delayed speech and language development\n- Seizure\n- Abnormal corpus callosum morphology\n- Absent speech\n- Joint hypermobility\n- Intellectual disability, profound\n- Delayed gross motor development\n- Epileptic spasm\n- Midface retrusion\n- Persistence of hemoglobin F\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10076.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High palate\n- Microcephaly\n- Full cheeks\n- Strabismus\n- Delayed speech and language development\n- Abnormal brainstem morphology\n- Scoliosis\n- Short stature\n- Depressed nasal bridge\n- Oromotor apraxia\n- Intellectual disability, severe\n- Speech apraxia\n- Hypoplasia of the midbrain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10077.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10078.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10079.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Smooth philtrum\n- Abnormality of the outer ear\n- Small earlobe\n- Overfolded helix\n- Protruding ear\n- Strabismus\n- Ptosis\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Spastic paraplegia\n- Absent speech\n- Gait ataxia\n- Broad-based gait\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Repetitive compulsive behavior\n- Attached earlobe\n- Moderate global developmental delay\n- Midface retrusion\n- Persistence of hemoglobin F\n- Neurodevelopmental delay\n- Squared superior portion of helix\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10080.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Smooth philtrum\n- Abnormality of the outer ear\n- Small earlobe\n- Overfolded helix\n- Protruding ear\n- Strabismus\n- Ptosis\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Spastic paraplegia\n- Absent speech\n- Gait ataxia\n- Broad-based gait\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Repetitive compulsive behavior\n- Attached earlobe\n- Moderate global developmental delay\n- Midface retrusion\n- Persistence of hemoglobin F\n- Neurodevelopmental delay\n- Squared superior portion of helix\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10081.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Epicanthus\n- Smooth philtrum\n- Abnormality of the outer ear\n- Small earlobe\n- Overfolded helix\n- Protruding ear\n- Strabismus\n- Ptosis\n- Atypical behavior\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Spastic paraplegia\n- Absent speech\n- Gait ataxia\n- Broad-based gait\n- Delayed gross motor development\n- Intellectual disability, moderate\n- Repetitive compulsive behavior\n- Attached earlobe\n- Moderate global developmental delay\n- Midface retrusion\n- Persistence of hemoglobin F\n- Neurodevelopmental delay\n- Squared superior portion of helix\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10082.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Pointed chin\n- Hypertelorism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10083.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10084.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10085.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Downslanted palpebral fissures\n- Global developmental delay\n- Growth delay\n- High pitched voice\n- Broad toe\n- Short stature\n- Deviated nasal septum\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10086.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10087.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10088.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10089.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Webbed neck\n- Downslanted palpebral fissures\n- Ptosis\n- Calcaneovalgus deformity\n- Genu valgum\n- Lumbar hyperlordosis\n- Disproportionate short-trunk short stature\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10090.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Narrow forehead\n- Low-set ears\n- Tapered finger\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10091.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Ptosis\n- Global developmental delay\n- Abnormal facial shape\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/10092.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Upslanted palpebral fissure\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/10093.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Microcephaly\n- Retrognathia\n- Epicanthus\n- Small earlobe\n- Prominent antihelix\n- Bulbous nose\n- Wide nasal bridge\n- Abnormal nasal tip morphology\n- Wide nose\n- Broad nasal tip\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Apraxia\n- Fine hair\n- Frontal upsweep of hair\n- Drooling\n- Intellectual disability, moderate\n- High anterior hairline\n- Persistence of hemoglobin F\n- Thick vermilion border\n- Wide nasal base\n- High posterior hairline\n- Oral motor hypotonia\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10094.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Retrognathia\n- Long philtrum\n- Hypertrichosis\n- Intellectual disability\n- Failure to thrive in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/10095.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Microcephaly\n- Epicanthus\n- Full cheeks\n- Abnormality of the outer ear\n- Wide nasal bridge\n- Strabismus\n- Downslanted palpebral fissures\n- Telecanthus\n- Hirsutism\n- Congenital hip dislocation\n- Joint hypermobility\n- Intellectual disability, moderate\n- Delayed skeletal maturation\n- Short stature\n- Prominent nasal tip\n- Medial flaring of the eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10096.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hyperopic astigmatism\n- Growth delay\n- Abnormal facial shape\n- Focal-onset seizure\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/10097.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atresia of the external auditory canal\n- Bilateral choanal atresia\n- Bilateral conductive hearing impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10098.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thrombocytopenia\n- Neutropenia\n- 3-Methylglutaconic aciduria\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/10099.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Triangular face\n- Telecanthus\n- Delayed eruption of primary teeth\n- Small for gestational age\n- Abnormal facial shape\n- High, narrow palate\n- Clinodactyly of the 5th finger\n- Recurrent bronchopulmonary infections\n- Postnatal growth retardation\n- Speech apraxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/10100.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Short upper lip\n- Mandibular prognathia\n- Hypertelorism\n- Hypoplasia of the maxilla\n- Low-set ears\n- Strabismus\n- Proptosis\n- Shallow orbits\n- Carious teeth\n- Dental crowding\n- Dental malocclusion\n- Frontal bossing\n- Abnormal calvaria morphology\n- Depressed nasal bridge\n- Anterior open-bite malocclusion\n- Ankyloglossia\n- Overjet\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10101.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypoplasia of the uterus\n- High palate\n- Low-set ears\n- Wide nasal bridge\n- Anteverted nares\n- Short neck\n- Strabismus\n- Nystagmus\n- Primary hypothyroidism\n- Hyperinsulinemia\n- Shield chest\n- Numerous nevi\n- Intellectual disability\n- Limited elbow extension\n- Obesity\n- Short columella\n- Frontal bossing\n- Hypertriglyceridemia\n- Delayed skeletal maturation\n- Cubitus valgus\n- Hyperlordosis\n- Short stature\n- Type II diabetes mellitus\n- Wide intermamillary distance\n- Rhizomelia\n- Joint contracture of the 5th finger\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/10102.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10103.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10104.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10105.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10106.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10107.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10108.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10109.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10110.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10111.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10112.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10113.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10114.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10115.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10116.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10117.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10118.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10119.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10120.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10121.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10122.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10123.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Malar flattening\n- Full cheeks\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Wide nasal bridge\n- Long neck\n- Periorbital fullness\n- Dental malocclusion\n- Intellectual disability, mild\n- Hoarse voice\n- Short nose\n- Short stature\n- Decreased body weight\n- Large earlobe\n- Broad eyebrow\n- Feeding difficulties\n- Thick vermilion border\n- Stellate iris\n- Auditory sensitivity\n- Systolic heart murmur\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10124.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10125.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10126.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thick upper lip vermilion\n- Velopharyngeal insufficiency\n- Retrognathia\n- Triangular nasal tip\n- Anteverted nares\n- Upslanted palpebral fissure\n- Synophrys\n- Pectus excavatum\n- Delayed puberty\n- Osteopenia\n- Prominent fingertip pads\n- Hyperreflexia\n- Hypernasal speech\n- Dysphonia\n- Short foot\n- Prominent glabella\n- Delayed gross motor development\n- Frontal upsweep of hair\n- Poor coordination\n- Highly arched eyebrow\n- Coxa valga\n- Downturned corners of mouth\n- Delayed skeletal maturation\n- Thoracic kyphosis\n- Micromelia\n- Dislocated radial head\n- Short nose\n- Clinodactyly of the 5th finger\n- Short stature\n- Short fourth metatarsal\n- Short fifth metatarsal\n- Limited elbow extension and supination\n- Premature fusion of phalangeal epiphyses\n- Lower limb hypertonia\n- Axial hypotonia\n- Absent epiphysis of the middle phalanx of the 5th finger\n- Forearm undergrowth\n- Thick vermilion border\n- Reduced arm span\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10127.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Micrognathia\n- Triangular nasal tip\n- Anteverted nares\n- Synophrys\n- Delayed speech and language development\n- Hyperextensibility of the finger joints\n- Dehydration\n- Deep philtrum\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Micromelia\n- Short nose\n- Short stature\n- Abnormal nasal dorsum morphology\n- Abnormality of mouth shape\n- Feeding difficulties\n- Thin toenail\n- Thin eyebrow\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10128.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Micrognathia\n- Triangular nasal tip\n- Anteverted nares\n- Synophrys\n- Delayed speech and language development\n- Hyperextensibility of the finger joints\n- Dehydration\n- Deep philtrum\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Micromelia\n- Short nose\n- Short stature\n- Abnormal nasal dorsum morphology\n- Abnormality of mouth shape\n- Feeding difficulties\n- Thin toenail\n- Thin eyebrow\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10129.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Microcephaly\n- Hypertelorism\n- Micrognathia\n- Triangular nasal tip\n- Anteverted nares\n- Synophrys\n- Delayed speech and language development\n- Hyperextensibility of the finger joints\n- Dehydration\n- Deep philtrum\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Micromelia\n- Short nose\n- Short stature\n- Abnormal nasal dorsum morphology\n- Abnormality of mouth shape\n- Feeding difficulties\n- Thin toenail\n- Thin eyebrow\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10130.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Cryptorchidism\n- Micropenis\n- Brachycephaly\n- Microcephaly\n- Posteriorly rotated ears\n- Anteverted nares\n- Long eyelashes\n- Synophrys\n- Single transverse palmar crease\n- Short foot\n- Short toe\n- Deep philtrum\n- Highly arched eyebrow\n- Radial bowing\n- obsolete Abnormality of the ulna\n- Absent radius\n- Aplasia of the ulna\n- Clinodactyly of the 5th finger\n- Short palm\n- Curved middle phalanx of the 5th finger\n- Short finger\n- Proximal placement of thumb\n- Short thumb\n- Curved 1st metacarpal\n- Prominent forehead\n- obsolete Small scrotum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10131.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Smooth philtrum\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Myopia\n- Synophrys\n- Widely spaced teeth\n- Microdontia\n- Cutis marmorata\n- Intellectual disability\n- Seizure\n- Absent speech\n- Toe syndactyly\n- Gastroesophageal reflux\n- Pneumonia\n- Asthma\n- Inability to walk\n- Highly arched eyebrow\n- Scoliosis\n- Downturned corners of mouth\n- Limited elbow movement\n- Short palm\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Lacrimal duct stenosis\n- Feeding difficulties in infancy\n- Aplasia of the fingers\n- Proximal placement of thumb\n- Localized hirsutism\n- Facial hirsutism\n- Abnormal digit morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10132.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Thin vermilion border\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Low-set ears\n- Long eyelashes\n- Synophrys\n- Hyperactivity\n- Hirsutism\n- Global developmental delay\n- Limited elbow extension\n- Small for gestational age\n- Short foot\n- Episodic vomiting\n- Downturned corners of mouth\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Decreased body weight\n- 2-3 toe syndactyly\n- Postnatal growth retardation\n- Delayed myelination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10133.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Long philtrum\n- Synophrys\n- Single transverse palmar crease\n- Global developmental delay\n- Motor delay\n- Short foot\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Short nose\n- Clinodactyly of the 5th finger\n- Short palm\n- Short stature\n- Decreased body weight\n- Postnatal growth retardation\n- Concave nasal ridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10134.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Low anterior hairline\n- Long philtrum\n- Low-set ears\n- Long eyelashes\n- Synophrys\n- Delayed speech and language development\n- Single transverse palmar crease\n- Hirsutism\n- Abnormal finger morphology\n- Depressed nasal bridge\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10135.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10136.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Synophrys\n- Neurodevelopmental abnormality\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10137.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Protruding ear\n- Depressed nasal tip\n- Long palpebral fissure\n- Intellectual disability, mild\n- Mild postnatal growth retardation\n- Ventricular septal defect\n- Talipes equinovarus\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10138.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10139.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10140.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10141.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10142.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Long philtrum\n- Wide nasal bridge\n- Myopia\n- Delayed speech and language development\n- Single transverse palmar crease\n- Intellectual disability\n- Spasticity\n- Motor delay\n- Myopathic facies\n- Asthma\n- Ventriculomegaly\n- Abnormality of speech or vocalization\n- Tetraparesis\n- Abnormal globus pallidus morphology\n- Aspiration\n- Feeding difficulties\n- Allergy\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, DYSMORPHIC FACIES, AND T-CELL ABNORMALITIES; IDDSFTA"}],"image":"exported_images\/10143.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Mandibular prognathia\n- Pointed chin\n- Short philtrum\n- Broad forehead\n- Sloping forehead\n- Posteriorly rotated ears\n- Sensorineural hearing impairment\n- Depressed nasal tip\n- Broad nasal tip\n- Strabismus\n- Rod-cone dystrophy\n- Exotropia\n- Upslanted palpebral fissure\n- Optic nerve hypoplasia\n- Delayed speech and language development\n- Hypotonia\n- Gastroesophageal reflux\n- Downturned corners of mouth\n- Obstructive sleep apnea\n- Short stature\n- Severe global developmental delay\n- Midface retrusion\n- Feeding difficulties\n- Anisometropia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/10144.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypertelorism\n- High forehead\n- Overfolded helix\n- Ptosis\n- Hypermetropia\n- Autistic behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability, mild\n- Motor delay\n- Joint laxity\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Almond-shaped palpebral fissure\n- Overweight\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/10145.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypertelorism\n- High forehead\n- Overfolded helix\n- Ptosis\n- Hypermetropia\n- Autistic behavior\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability, mild\n- Motor delay\n- Joint laxity\n- Poor fine motor coordination\n- Attention deficit hyperactivity disorder\n- Almond-shaped palpebral fissure\n- Overweight\n- Overfriendliness\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/10146.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Wide nose\n- Depressed nasal ridge\n- Macrodontia of permanent maxillary central incisor\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Hip dysplasia\n- Downturned corners of mouth\n- Preauricular pit\n- Facial hirsutism\n- Delayed fine motor development\n- Delayed myelination\n- Glue ear\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES; IDDSADF"}],"image":"exported_images\/10147.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Recurrent otitis media\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Cataract\n- Proptosis\n- Shallow orbits\n- Widely spaced teeth\n- Pectus carinatum\n- Prominent scalp veins\n- Retinal atrophy\n- Limited elbow extension\n- Oligohydramnios\n- Calcaneovalgus deformity\n- Short distal phalanx of toe\n- Thoracic kyphosis\n- Elbow flexion contracture\n- Limited knee extension\n- Hypoplasia of the odontoid process\n- Severe short stature\n- Decreased body weight\n- Apneic episodes in infancy\n- Knee flexion contracture\n- Limited shoulder movement\n- Abnormality of retinal pigmentation\n- Acetabular dysplasia\n- Short distal phalanx of finger\n- Dermal translucency\n- High myopia\n- Prominent forehead\n- Upbeat nystagmus\n- Midface retrusion\n- Anterior wedging of T12\n- Tympanosclerosis\n- Posterior staphyloma\n- Pseudophakia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/10148.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Ectopic kidney\n- Microcephaly\n- Micrognathia\n- Wide nasal bridge\n- Prominent nose\n- Microdontia\n- Poikiloderma\n- Intellectual disability, mild\n- Selective tooth agenesis\n- Anemia\n- Hypoplastic iliac wing\n- Narrow pelvis bone\n- Severe short stature\n- Decreased body weight\n- Atrophy of alveolar ridges\n- Short dental root\n- Pulp obliteration\n- Cerebral dysmyelination\n- Low hanging columella\n- Abnormal incisor morphology\n- Rootless teeth\n- Abnormality of canine\n- Increased overbite\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE II; MOPD2"}],"image":"exported_images\/10149.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Macrocephaly\n- Dolichocephaly\n- Long eyelashes\n- Pectus excavatum\n- Hyperpigmentation of the skin\n- Dry skin\n- Hemangioma\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Joint laxity\n- Abnormal mitral valve morphology\n- Patent ductus arteriosus\n- Slow-growing hair\n- Short stature\n- Decreased body weight\n- Attention deficit hyperactivity disorder\n- Palmoplantar cutis laxa\n- Sparse hair\n- Delayed fine motor development\n- Prominent forehead\n- Feeding difficulties\n- Extra-axial cerebrospinal fluid accumulation\n- Nasogastric tube feeding\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/10150.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Broad nasal tip\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Broad nail\n- Bilateral tonic-clonic seizure\n- Sleep disturbance\n- Poor speech\n- obsolete Slowly progressive spastic quadriparesis\n- Tented upper lip vermilion\n- EEG with generalized slow activity\n- EEG with focal epileptiform discharges\n- Brain atrophy\n- obsolete Psychomotor retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10151.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cleft palate\n- Hypertelorism\n- Wide nasal bridge\n- Prominent nose\n- Strabismus\n- Long palpebral fissure\n- Autistic behavior\n- Hyperactivity\n- Hypotonia\n- Motor delay\n- Laryngomalacia\n- Highly arched eyebrow\n- Elevated circulating alkaline phosphatase concentration\n- Short nose\n- High hypermetropia\n- Large earlobe\n- Tented upper lip vermilion\n- Intellectual disability, severe\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10152.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Astigmatism\n- Strabismus\n- Seizure\n- Global developmental delay\n- Attention deficit hyperactivity disorder\n- Intellectual disability, severe\n- Alternating exotropia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/10153.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypermetropia\n- Compulsive behaviors\n- Abnormality of the skeletal system\n- Global developmental delay\n- Disproportionate tall stature\n- Intellectual disability, moderate\n- Focal-onset seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 62; MRD62"}],"image":"exported_images\/10154.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Myopia\n- Compulsive behaviors\n- Anxiety\n- Jaundice\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Aphasia\n- Speech articulation difficulties\n- Fatigue\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"O'DONNELL-LURIA-RODAN SYNDROME; ODLURO"}],"image":"exported_images\/10155.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Strabismus\n- Ptosis\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Single transverse palmar crease\n- Hypotonia\n- Poor speech\n- Depressed nasal bridge\n- Broad columella\n- Prominent forehead\n- Severe global developmental delay\n- Clinodactyly of the 4th finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 87; DEE87"}],"image":"exported_images\/10156.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prominent antihelix\n- Carious teeth\n- Dental crowding\n- Abnormal dental enamel morphology\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Exaggerated cupid's bow\n- Febrile seizure (within the age range of 3 months to 6 years)\n- High, narrow palate\n- Clinodactyly of the 5th finger\n- Preauricular pit\n- Prominent crus of helix\n- Supernumerary tooth\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/10157.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prominent antihelix\n- Carious teeth\n- Dental crowding\n- Abnormal dental enamel morphology\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Exaggerated cupid's bow\n- Febrile seizure (within the age range of 3 months to 6 years)\n- High, narrow palate\n- Clinodactyly of the 5th finger\n- Preauricular pit\n- Prominent crus of helix\n- Supernumerary tooth\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/10158.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Hypertelorism\n- Prominent supraorbital ridges\n- Downslanted palpebral fissures\n- Autistic behavior\n- Intellectual disability\n- Sleep disturbance\n- Developmental regression\n- Abnormality of the gastrointestinal tract\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/10159.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Smooth philtrum\n- Triangular face\n- Narrow forehead\n- Long philtrum\n- Strabismus\n- Delayed speech and language development\n- Hypotonia\n- Large for gestational age\n- Large forehead\n- Delayed skeletal maturation\n- Progressive macrocephaly\n- Mixed hypo- and hyperpigmentation of the skin\n- Intellectual disability, severe\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-KINGSMORE SYNDROME; SKS"}],"image":"exported_images\/10160.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Long face\n- Abnormal repetitive mannerisms\n- Seizure\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Hip dysplasia\n- Dysphagia\n- Constipation\n- EEG abnormality\n- Focal impaired awareness seizure\n- Abnormal cerebral white matter morphology\n- Scoliosis\n- Temperature instability\n- Intellectual disability, severe\n- Abnormal social behavior\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/10161.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Strabismus\n- Delayed speech and language development\n- Tapered finger\n- Intellectual disability\n- Hypotonia\n- Motor delay\n- Neonatal hypotonia\n- Absent speech\n- Joint laxity\n- Bradycardia\n- Constipation\n- Apnea\n- Exaggerated startle response\n- Depressed nasal bridge\n- Deep palmar crease\n- Feeding difficulties in infancy\n- High anterior hairline\n- Dilation of Virchow-Robin spaces\n- Tube feeding\n- Low levels of vitamin D\n- Hypersomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH NEONATAL RESPIRATORY INSUFFICIENCY, HYPOTONIA, AND FEEDING DIFFICULTIES; NEDRIHF"}],"image":"exported_images\/10162.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormal palate morphology\n- Large fontanelles\n- Low anterior hairline\n- Mandibular prognathia\n- Round face\n- Hypertelorism\n- Broad nasal tip\n- Thick eyebrow\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Reduced eye contact\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Absent speech\n- Pes planus\n- Short toe\n- Bilateral tonic-clonic seizure\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Mutism\n- Developmental regression\n- Focal impaired awareness seizure\n- Clinodactyly of the 5th finger\n- Short stature\n- Relative macrocephaly\n- Bilateral single transverse palmar creases\n- Atonic seizure\n- Focal emotional seizure with laughing\n- Prominent forehead\n- Abnormal social behavior\n- Thick vermilion border\n- Neurodevelopmental delay\n- Tonic seizure\n- Myoclonic seizure\n- Motor regression\n- Reduced blood 5-methyltetrahydrofolate level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10163.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Prominent nose\n- Short stature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/10164.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Short philtrum\n- High forehead\n- Low-set ears\n- Broad nasal tip\n- Astigmatism\n- Strabismus\n- Deeply set eye\n- Hypotelorism\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Hyperactivity\n- Seizure\n- Hypotonia\n- Motor delay\n- Absent speech\n- Constipation\n- Intellectual disability, moderate\n- Sleep disturbance\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, TURNER TYPE; MRXST"}],"image":"exported_images\/10165.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Long philtrum\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Anteverted nares\n- Pulmonic stenosis\n- Obstructive sleep apnea\n- Short nose\n- Spina bifida occulta\n- Symphalangism affecting the phalanges of the toes\n- Mild global developmental delay\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies"}],"image":"exported_images\/10166.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Ventriculomegaly\n- Sleep disturbance\n- Sleep apnea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/10167.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Seizure\n- Global developmental delay\n- Failure to thrive\n- Chronic diarrhea\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HAO-FOUNTAIN SYNDROME; HAFOUS"}],"image":"exported_images\/10168.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Intellectual disability\n- Seizure\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/10169.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypotelorism\n- Agenesis of corpus callosum\n- Hypertonia\n- Growth delay\n- Bilateral tonic-clonic seizure\n- Alobar holoprosencephaly\n- Median cleft lip and palate\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HARTSFIELD SYNDROME; HRTFDS"}],"image":"exported_images\/10170.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long palpebral fissure\n- Short stature\n- Eversion of lateral third of lower eyelids\n- Postnatal growth retardation\n- Short 5th finger\n- Intellectual disability, severe\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10171.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10172.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microglossia\n- Cleft palate\n- Microretrognathia\n- Broad nasal tip\n- Anteverted nares\n- Ptosis\n- Motor delay\n- Growth delay\n- Pulmonary arterial hypertension\n- Scoliosis\n- Congenital contracture\n- Myopathy\n- Elevated circulating creatine kinase concentration\n- Pectoralis hypoplasia\n- Hypoplasia of the musculature\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CAREY-FINEMAN-ZITER SYNDROME; CFZS"}],"image":"exported_images\/10173.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the genital system\n- Abnormality of the dentition\n- Abnormality of the eye\n- Delayed speech and language development\n- Intellectual disability\n- Motor delay\n- Hip dysplasia\n- Short stature\n- Distributed along Blaschko lines\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99, SYNDROMIC, FEMALE-RESTRICTED; MRXS99F"}],"image":"exported_images\/10174.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Narrow mouth\n- Trismus\n- Hypertelorism\n- Micrognathia\n- Low-set ears\n- Small earlobe\n- Protruding ear\n- Downslanted palpebral fissures\n- Ptosis\n- Synophrys\n- Delayed speech and language development\n- Single transverse palmar crease\n- Tapered finger\n- Seizure\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Plagiocephaly\n- Laryngomalacia\n- Hypoplasia of the corpus callosum\n- Enlarged cisterna magna\n- Obstructive sleep apnea\n- Central apnea\n- Simplified gyral pattern\n- Prominent ear helix\n- Horizontal eyebrow\n- Narrow nail\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"XIA-GIBBS SYNDROME; XIGIS"}],"image":"exported_images\/10175.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Narrow palate\n- Hypertelorism\n- Short philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Hypermetropia\n- Thick eyebrow\n- Optic nerve hypoplasia\n- Dental malocclusion\n- Delayed speech and language development\n- Hypothyroidism\n- Hypotonia\n- Global developmental delay\n- Gastroesophageal reflux\n- Bilateral tonic-clonic seizure\n- Delayed gross motor development\n- Frontal upsweep of hair\n- Gastroparesis\n- Gastrointestinal dysmotility\n- Tracheomalacia\n- Fused cervical vertebrae\n- Butterfly vertebrae\n- Feeding difficulties in infancy\n- Narrow naris\n- Central sleep apnea\n- Delayed fine motor development\n- Cerebral white matter hypoplasia\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/10176.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Small earlobe\n- Ptosis\n- Delayed speech and language development\n- Intellectual disability\n- Global developmental delay\n- Joint hypermobility\n- Delayed gross motor development\n- Frontal upsweep of hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND PTOSIS; IDDDFP"}],"image":"exported_images\/10177.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Esotropia\n- Hypotonia\n- Muscle weakness\n- Absent speech\n- Short foot\n- Constipation\n- Abnormality of thyroid physiology\n- Short palm\n- Atypical absence seizure\n- Atonic seizure\n- EEG with spike-wave complexes\n- Intellectual disability, severe\n- Severe global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hypotonia, infantile, with psychomotor retardation and characteristic facies"}],"image":"exported_images\/10178.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Wide mouth\n- Accessory oral frenulum\n- Thin upper lip vermilion\n- Microcephaly\n- Hearing impairment\n- Blue sclerae\n- Brachydactyly\n- Intellectual disability\n- Hypotonia\n- Absent speech\n- Joint laxity\n- Abnormal heart morphology\n- Coarctation of aorta\n- Gait imbalance\n- 4-5 toe syndactyly\n- Ankyloglossia\n- Feeding difficulties\n- Clinodactyly\n- Abnormality of movement\n- Cerebral visual impairment\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"YOU-HOOVER-FONG SYNDROME; YHFS"}],"image":"exported_images\/10179.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microtia\n- 2-4 finger syndactyly\n- Unicoronal synostosis\n- Urethral stricture\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/10180.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Long face\n- Short chin\n- High forehead\n- Low-set, posteriorly rotated ears\n- Small earlobe\n- Prominent nasal bridge\n- Strabismus\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Ataxia\n- Motor delay\n- Deep philtrum\n- Short stature\n- Horizontal eyebrow\n- Broad chin\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOTONIA, ATAXIA, AND DELAYED DEVELOPMENT SYNDROME; HADDS"}],"image":"exported_images\/10181.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Synophrys\n- Hypertrichosis\n- Nevus flammeus\n- Seizure\n- Atrial septal defect\n- Recurrent hypoglycemia\n- Prominent glabella\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Limb hypertonia\n- Highly arched eyebrow\n- Scoliosis\n- Deep palmar crease\n- Severe muscular hypotonia\n- Feeding difficulties in infancy\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/10182.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Posteriorly rotated ears\n- Broad nasal tip\n- Ptosis\n- Proptosis\n- Synophrys\n- Hypertrichosis\n- Nevus flammeus\n- Seizure\n- Atrial septal defect\n- Recurrent hypoglycemia\n- Prominent glabella\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Limb hypertonia\n- Highly arched eyebrow\n- Scoliosis\n- Deep palmar crease\n- Severe muscular hypotonia\n- Feeding difficulties in infancy\n- Capillary malformation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHASHI-PENA SYNDROME; SHAPNS"}],"image":"exported_images\/10183.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad alveolar ridges\n- Open mouth\n- Coarse facial features\n- Widely spaced teeth\n- Atypical behavior\n- Global developmental delay\n- Slender build\n- Broad-based gait\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Clinodactyly of the 5th finger\n- Depressed nasal bridge\n- Leg muscle stiffness\n- Midface retrusion\n- Right aortic arch\n- Thick vermilion border\n- Pineal cyst\n- Abnormal Eustachian tube morphology\n- Lateral ventricular asymmetry\n- Hyperplasia of the maxilla\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/10184.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Open mouth\n- Gingival overgrowth\n- Microcephaly\n- Coarse facial features\n- Full cheeks\n- Narrow forehead\n- Anteverted nares\n- Abnormal conjunctiva morphology\n- Delayed eruption of primary teeth\n- Widely spaced teeth\n- Seizure\n- Global developmental delay\n- Hemiparesis\n- Pachygyria\n- Failure to thrive\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Gastroesophageal reflux\n- Scoliosis\n- Abnormality of the knee\n- Short nasal bridge\n- Short stature\n- Prominent nasal tip\n- Chalazion\n- Osteopathia striata\n- Intellectual disability, severe\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SKRABAN-DEARDORFF SYNDROME; SKDEAS"}],"image":"exported_images\/10185.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Wide nasal bridge\n- Ptosis\n- Oculomotor apraxia\n- Intellectual disability, mild\n- Dysarthria\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Large for gestational age\n- Frontal bossing\n- Gait ataxia\n- Polymicrogyria\n- Depressed nasal bridge\n- Postaxial polydactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/10186.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Epicanthus\n- Smooth philtrum\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Specific learning disability\n- Intellectual disability, moderate\n- Language impairment\n- Short palm\n- Short stature\n- Decreased body weight\n- Depressed nasal bridge\n- Bilateral single transverse palmar creases\n- Intellectual disability, severe\n- Malar rash\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL KAISSI SYNDROME; ALKAS"}],"image":"exported_images\/10187.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Brachycephaly\n- Wide anterior fontanel\n- Mandibular prognathia\n- Broad forehead\n- Low-set ears\n- Conductive hearing impairment\n- Abnormal eyelid morphology\n- Downslanted palpebral fissures\n- Hypermetropia\n- Microphthalmia\n- Microdontia\n- Hypertrichosis\n- obsolete Decreased subcutaneous fat\n- Global developmental delay\n- Dandy-Walker malformation\n- Failure to thrive\n- Intrauterine growth retardation\n- Small for gestational age\n- Umbilical hernia\n- Left ventricular hypertrophy\n- Small nail\n- Coarse hair\n- High, narrow palate\n- Short stature\n- Coronal craniosynostosis\n- Partial abdominal muscle agenesis\n- Excessive wrinkled skin\n- Abnormality of the hairline\n- Short distal phalanx of finger\n- Underdeveloped supraorbital ridges\n- Dermal translucency\n- Primary microcephaly\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FONTAINE PROGEROID SYNDROME; FPS"}],"image":"exported_images\/10188.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Malar flattening\n- Epicanthus\n- Short philtrum\n- Autistic behavior\n- Neonatal hypotonia\n- Atrial septal defect\n- Pes planus\n- Short nose\n- Short stature\n- Depressed nasal bridge\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OKUR-CHUNG NEURODEVELOPMENTAL SYNDROME; OCNDS"}],"image":"exported_images\/10189.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Abnormality of the philtrum\n- Wide nasal bridge\n- Strabismus\n- Abnormality of the ear\n- Atypical behavior\n- Hypotonia\n- Abnormal joint morphology\n- Pes planus\n- Sleep disturbance\n- Intellectual disability, borderline\n- Feeding difficulties\n- Abnormality of brain morphology\n- Down-sloping shoulders\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/10190.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin vermilion border\n- Macrocephaly\n- Abnormality of the philtrum\n- Abnormality of the eye\n- Abnormality of the ear\n- Atypical behavior\n- Gynecomastia\n- Pes planus\n- Sleep disturbance\n- Intellectual disability, borderline\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/10191.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Hypertelorism\n- Smooth philtrum\n- Small forehead\n- Flared nostrils\n- Broad nasal tip\n- Optic disc pallor\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Hypothyroidism\n- Eczema\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Flexion contracture\n- Small for gestational age\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Thrombocytopenia\n- Ventriculomegaly\n- Scoliosis\n- Recurrent infections\n- Immunodeficiency\n- Distal arthrogryposis\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Medial flaring of the eyebrow\n- Dilatation of the renal pelvis\n- Increased mean platelet volume\n- Camptodactyly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/10192.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Cleft palate\n- Thin upper lip vermilion\n- Microcephaly\n- Hypertelorism\n- Smooth philtrum\n- Small forehead\n- Flared nostrils\n- Broad nasal tip\n- Optic disc pallor\n- Upslanted palpebral fissure\n- Widely spaced teeth\n- Hypothyroidism\n- Eczema\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Flexion contracture\n- Small for gestational age\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Thrombocytopenia\n- Ventriculomegaly\n- Scoliosis\n- Recurrent infections\n- Immunodeficiency\n- Distal arthrogryposis\n- Postnatal growth retardation\n- Abnormal hair whorl\n- Medial flaring of the eyebrow\n- Dilatation of the renal pelvis\n- Increased mean platelet volume\n- Camptodactyly\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TAKENOUCHI-KOSAKI SYNDROME; TKS"}],"image":"exported_images\/10193.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Low anterior hairline\n- Hypertelorism\n- Wide nasal bridge\n- Downslanted palpebral fissures\n- Synophrys\n- Horizontal nystagmus\n- Atypical behavior\n- Agitation\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Sacral dimple\n- Facial erythema\n- Intellectual disability\n- Global developmental delay\n- Dextrocardia\n- Anemia\n- Bilateral tonic-clonic seizure\n- Low posterior hairline\n- Opisthotonus\n- Enlarged cisterna magna\n- Sleep disturbance\n- Downturned corners of mouth\n- Inferior cerebellar vermis hypoplasia\n- EEG with focal spikes\n- Abnormal hypothalamus morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 66; DEE66"}],"image":"exported_images\/10194.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, growth restriction and increased sister chromatid exchange"}],"image":"exported_images\/10195.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Protruding ear\n- Strabismus\n- Nystagmus\n- Intellectual disability, mild\n- Long toe\n- Abnormal optic disc morphology\n- Cerebral visual impairment\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSCH-BOONSTRA-SCHAAF OPTIC ATROPHY SYNDROME; BBSOAS"}],"image":"exported_images\/10196.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Retrognathia\n- High forehead\n- Hearing impairment\n- Choanal stenosis\n- Proptosis\n- Blue sclerae\n- Hypertrichosis\n- Global developmental delay\n- Pachygyria\n- Umbilical hernia\n- Hypoplasia of the corpus callosum\n- Decreased circulating IgA level\n- Abnormal respiratory system physiology\n- Short nose\n- Severe global developmental delay\n- Midface retrusion\n- Abnormal bone ossification\n- Long fingers\n- Hyperplasia of the maxilla\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL-SMITH SYNDROME; MRSHSS"}],"image":"exported_images\/10197.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Square face\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Broad neck\n- Microphthalmia\n- Optic nerve hypoplasia\n- Horizontal nystagmus\n- Pectus excavatum\n- Nevus flammeus\n- Global developmental delay\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Micromelia\n- Short stature\n- Pes valgus\n- Branchial cyst\n- Upper limb undergrowth\n- Asymmetry of the ears\n- Prominent forehead\n- Feeding difficulties\n- Esodeviation\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/10198.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Triangular mouth\n- Epicanthus\n- Short philtrum\n- Broad forehead\n- Synophrys\n- Irritability\n- Delayed speech and language development\n- Hemangioma\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Specific learning disability\n- Dystonia\n- Absent speech\n- Vomiting\n- Myotonia\n- Supernumerary nipple\n- Nevus\n- Clinodactyly of the 5th finger\n- 2-3 toe syndactyly\n- Abnormal dermatoglyphics\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HIATT-NEU-COOPER NEURODEVELOPMENTAL SYNDROME; HINCONS"}],"image":"exported_images\/10199.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Urinary retention\n- Inguinal hernia\n- Tall stature\n- High palate\n- Macrocephaly\n- Dolichocephaly\n- Pointed chin\n- Triangular face\n- Low-set, posteriorly rotated ears\n- Strabismus\n- Deeply set eye\n- Long eyelashes\n- Synophrys\n- Pectus excavatum\n- Numerous nevi\n- Arachnodactyly\n- Large hands\n- Motor delay\n- Generalized hypotonia\n- Specific learning disability\n- Large for gestational age\n- Ventricular septal defect\n- Atrial septal defect\n- Patent ductus arteriosus\n- Tachycardia\n- Overlapping toe\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Vertigo\n- Expressive language delay\n- Highly arched eyebrow\n- Scoliosis\n- Short nose\n- Generalized hypertrichosis\n- Depressed nasal bridge\n- Recurrent pneumonia\n- Chiari type I malformation\n- Hypoplastic helices\n- Laryngotracheomalacia\n- Optic nerve glioma\n- Large earlobe\n- Lymphatic vessel neoplasm\n- Osteochondroma\n- Mesenteric cyst\n- Dysuria\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES; IDDCDF"}],"image":"exported_images\/10200.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Square face\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Broad neck\n- Microphthalmia\n- Optic nerve hypoplasia\n- Horizontal nystagmus\n- Pectus excavatum\n- Nevus flammeus\n- Global developmental delay\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Micromelia\n- Short stature\n- Pes valgus\n- Branchial cyst\n- Upper limb undergrowth\n- Asymmetry of the ears\n- Prominent forehead\n- Feeding difficulties\n- Esodeviation\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/10201.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Full cheeks\n- Square face\n- Narrow forehead\n- Long philtrum\n- Micrognathia\n- Posteriorly rotated ears\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Broad neck\n- Microphthalmia\n- Optic nerve hypoplasia\n- Horizontal nystagmus\n- Pectus excavatum\n- Nevus flammeus\n- Global developmental delay\n- Intrauterine growth retardation\n- Ventricular septal defect\n- Micromelia\n- Short stature\n- Pes valgus\n- Branchial cyst\n- Upper limb undergrowth\n- Asymmetry of the ears\n- Prominent forehead\n- Feeding difficulties\n- Esodeviation\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/10202.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Open mouth\n- Delayed speech and language development\n- Hyperactivity\n- Spastic diplegia\n- Motor delay\n- Polyhydramnios\n- Patent ductus arteriosus\n- Constipation\n- Ventriculomegaly\n- Polymicrogyria\n- Recurrent respiratory infections\n- Incoordination\n- Limb hypertonia\n- Obstructive sleep apnea\n- Carotid artery tortuosity\n- Attention deficit hyperactivity disorder\n- Axial hypotonia\n- Intraventricular hemorrhage\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TURNPENNY-FRY SYNDROME; TPFS"}],"image":"exported_images\/10203.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- High forehead\n- Broad nasal tip\n- Anteverted nares\n- Delayed speech and language development\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Large for gestational age\n- Attention deficit hyperactivity disorder\n- Abnormal temper tantrums\n- Histiocytosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT; MACID"}],"image":"exported_images\/10204.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Short foot\n- Polyphagia\n- Increased body weight\n- Feeding difficulties\n- Skin-picking\n- Chronic constipation\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/10205.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Short foot\n- Gastroesophageal reflux\n- Polyphagia\n- Kyphoscoliosis\n- Increased body weight\n- Temperature instability\n- Sleep apnea\n- Feeding difficulties\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/10206.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypogonadism\n- Abnormality of the eye\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Neonatal hypotonia\n- Flexion contracture\n- Gastroesophageal reflux\n- Kyphoscoliosis\n- Short stature\n- Feeding difficulties\n- Skin-picking\n- Chronic constipation\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/10207.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypoplastic male external genitalia\n- Micropenis\n- Hypogonadism\n- Round face\n- Narrow forehead\n- Abnormality of the eye\n- Atypical behavior\n- Autistic behavior\n- Abnormal repetitive mannerisms\n- Gynecomastia\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Neonatal hypotonia\n- Hip dysplasia\n- Failure to thrive\n- Obesity\n- Short foot\n- Poor suck\n- Polyphagia\n- Central apnea\n- Increased body weight\n- Almond-shaped palpebral fissure\n- Speech articulation difficulties\n- Sleep apnea\n- Feeding difficulties\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHAAF-YANG SYNDROME; SHFYNG"}],"image":"exported_images\/10208.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cleft palate\n- Long face\n- Hypoplasia of the maxilla\n- Micrognathia\n- Low-set ears\n- Abnormal pinna morphology\n- Stenosis of the external auditory canal\n- Recurrent otitis media\n- Deeply set eye\n- Downslanted palpebral fissures\n- Microdontia\n- Diastema\n- Atypical behavior\n- Self-mutilation\n- Seizure\n- Decreased fetal movement\n- Short foot\n- Dysphagia\n- Poor suck\n- Lower limb spasticity\n- Broad-based gait\n- External genital hypoplasia\n- Sparse hair\n- Postnatal growth retardation\n- Intellectual disability, severe\n- Hypoplastic fifth toenail\n- High-pitched cry\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/10209.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROFACIAL DYSOSTOSIS 1, NAGER TYPE; AFD1"}],"image":"exported_images\/10210.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Micrognathia\n- Narrow chest\n- Anal stenosis\n- Scoliosis\n- Posterior rib gap\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBROCOSTOMANDIBULAR SYNDROME; CCMS"}],"image":"exported_images\/10211.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Low-set ears\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/10212.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/10213.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ZTTK SYNDROME; ZTTKS"}],"image":"exported_images\/10214.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Microretrognathia\n- Hypermetropia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypernasal speech\n- Constipation\n- Recurrent upper respiratory tract infections\n- Tooth agenesis\n- Abnormality of canine\n- Feeding difficulties\n- Flat face\n- Camptodactyly\n- Short palpebral fissure\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/10215.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Microretrognathia\n- Hypermetropia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypernasal speech\n- Constipation\n- Recurrent upper respiratory tract infections\n- Tooth agenesis\n- Abnormality of canine\n- Feeding difficulties\n- Flat face\n- Camptodactyly\n- Short palpebral fissure\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/10216.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Epicanthus\n- Microretrognathia\n- Hypermetropia\n- Blepharophimosis\n- Upslanted palpebral fissure\n- Autistic behavior\n- Hypernasal speech\n- Constipation\n- Recurrent upper respiratory tract infections\n- Tooth agenesis\n- Abnormality of canine\n- Feeding difficulties\n- Flat face\n- Camptodactyly\n- Short palpebral fissure\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/10217.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Square face\n- Long philtrum\n- Low-set ears\n- Protruding ear\n- Depressed nasal ridge\n- Anteverted nares\n- Strabismus\n- Telecanthus\n- Ptosis\n- Upslanted palpebral fissure\n- Autistic behavior\n- Short columella\n- Deep philtrum\n- Highly arched eyebrow\n- Short nose\n- Clinodactyly of the 5th finger\n- Postnatal growth retardation\n- Deviation of the hallux\n- Broad hallux\n- 4-5 finger syndactyly\n- Everted upper lip vermilion\n- Intellectual disability, severe\n- Flat face\n- Short palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Menke-Hennekam syndrome"}],"image":"exported_images\/10218.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Strabismus\n- Deeply set eye\n- Atypical behavior\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Dysarthria\n- Intellectual disability, moderate\n- External genital hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/10219.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Strabismus\n- Deeply set eye\n- Atypical behavior\n- Delayed speech and language development\n- Ataxia\n- Hypotonia\n- Dysarthria\n- Intellectual disability, moderate\n- External genital hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, BILLUART TYPE; MRXSBL"}],"image":"exported_images\/10220.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Pointed chin\n- Broad nasal tip\n- Strabismus\n- Telecanthus\n- Ptosis\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Hyperactivity\n- Hypotonia\n- Intellectual disability, mild\n- Motor delay\n- Increased serum lactate\n- Sleep disturbance\n- Short stature\n- Depressed nasal bridge\n- Abnormality of dental morphology\n- Mildly elevated creatine kinase\n- Feeding difficulties in infancy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIETS-JONGMANS SYNDROME; DIJOS"}],"image":"exported_images\/10221.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY; IMAGEI"}],"image":"exported_images\/10222.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal palate morphology\n- Thick lower lip vermilion\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Thick eyebrow\n- Hyperpigmentation of the skin\n- Seizure\n- Abnormal corpus callosum morphology\n- Absent speech\n- Failure to thrive\n- Poor suck\n- Abnormal 5th finger morphology\n- Sparse hair\n- Feeding difficulties in infancy\n- Abnormal fifth toe morphology\n- Severe global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10223.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- High palate\n- Everted lower lip vermilion\n- Brachycephaly\n- Microcephaly\n- Epicanthus\n- Hypertelorism\n- Broad forehead\n- Low-set, posteriorly rotated ears\n- Protruding ear\n- Anteverted nares\n- Exotropia\n- Delayed speech and language development\n- Motor delay\n- Short nose\n- Depressed nasal bridge\n- Tented upper lip vermilion\n- U-Shaped upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/10224.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Trigonocephaly\n- Microcephaly\n- Epicanthus\n- Delayed eruption of permanent teeth\n- Cerebellar atrophy\n- Spastic tetraparesis\n- Laryngomalacia\n- Rocker bottom foot\n- Abnormal cerebral white matter morphology\n- Clinodactyly of the 5th finger\n- Decreased body weight\n- Prominent metopic ridge\n- Axial hypotonia\n- Intellectual disability, severe\n- Infra-orbital fold\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10225.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Low-set, posteriorly rotated ears\n- Narrow nose\n- Telecanthus\n- Global developmental delay\n- Almond-shaped palpebral fissure\n- Microtia\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/10226.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Low-set, posteriorly rotated ears\n- Narrow nose\n- Telecanthus\n- Global developmental delay\n- Almond-shaped palpebral fissure\n- Microtia\n- Broad eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM; DEDDFA"}],"image":"exported_images\/10227.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Gingival overgrowth\n- Widow's peak\n- Thickened helices\n- Underdeveloped nasal alae\n- Bifid nasal tip\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Upslanted palpebral fissure\n- Hirsutism\n- Abnormal palmar dermatoglyphics\n- Tapered finger\n- Intellectual disability, mild\n- Global developmental delay\n- Generalized hypotonia\n- Joint hypermobility\n- Anonychia\n- Short toe\n- Deep philtrum\n- Increased body weight\n- Prominent nasal septum\n- Laterally curved eyebrow\n- Short finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Zimmermann-Laband syndrome"}],"image":"exported_images\/10228.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Hypohidrosis\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Deep philtrum\n- Elevated circulating alkaline phosphatase concentration\n- Elevated circulating creatine kinase concentration\n- Uplifted earlobe\n- Abnormal digit morphology\n- Chin with horizontal crease\n- Scaling skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 80; DEE80"}],"image":"exported_images\/10229.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Horizontal nystagmus\n- Hypotonia\n- Limb ataxia\n- Truncal ataxia\n- Inability to walk\n- Paroxysmal tonic upgaze\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Spinocerebellar ataxia, autosomal recessive"}],"image":"exported_images\/10230.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Coarse facial features\n- Low anterior hairline\n- Hypertelorism\n- Short philtrum\n- Small forehead\n- Macrotia\n- Convex nasal ridge\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Aggressive behavior\n- Delayed speech and language development\n- Hypertrichosis\n- Global developmental delay\n- Joint laxity\n- Obesity\n- Short foot\n- Short toe\n- Intellectual disability, moderate\n- Poor head control\n- Expressive language delay\n- Genu valgum\n- Poor hand-eye coordination\n- Anterior pituitary hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/10231.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Deeply set eye\n- Esotropia\n- Nasolacrimal duct obstruction\n- Decreased response to growth hormone stimulation test\n- Brachydactyly\n- Obesity\n- Gastroesophageal reflux\n- Generalized non-motor (absence) seizure\n- Sleep disturbance\n- Polyphagia\n- Inverted nipples\n- Short stature\n- Axial hypotonia\n- Mild global developmental delay\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/10232.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10233.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Macrocephaly\n- Long face\n- Full cheeks\n- Mandibular prognathia\n- High forehead\n- Deeply set eye\n- Hypermetropia\n- Amblyopia\n- Delayed speech and language development\n- Slender finger\n- Hypotonia\n- Motor delay\n- Myoclonus\n- Overgrowth\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES; DDVIBA"}],"image":"exported_images\/10234.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Absent speech\n- Intellectual disability, profound\n- Hyperkinetic movements\n- Hypsarrhythmia\n- Scoliosis\n- Infantile muscular hypotonia\n- Overlapping fingers\n- Otitis media with effusion\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/10235.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Seizure\n- Hypotonia\n- Absent speech\n- Intellectual disability, profound\n- Hyperkinetic movements\n- Hypsarrhythmia\n- Scoliosis\n- Infantile muscular hypotonia\n- Overlapping fingers\n- Otitis media with effusion\n- Cerebral visual impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES; CHEDDA"}],"image":"exported_images\/10236.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Underdeveloped nasal alae\n- Broad nasal tip\n- Anteverted nares\n- Autism\n- Abnormal repetitive mannerisms\n- Hypotonia\n- Overlapping toe\n- Exaggerated cupid's bow\n- Short nose\n- Microtia\n- Upper eyelid edema\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/10237.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Wide nasal bridge\n- Esotropia\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Sacral dimple\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Supernumerary nipple\n- Medial flaring of the eyebrow\n- Delayed fine motor development\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/10238.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Joint hypermobility\n- Intellectual disability, moderate\n- Finger syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/10239.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Autistic behavior\n- Motor delay\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/10240.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Microcephaly\n- Hearing impairment\n- Amblyopia\n- Delayed speech and language development\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WHITE-SUTTON SYNDROME; WHSUS"}],"image":"exported_images\/10241.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Conductive hearing impairment\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Delayed speech and language development\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10242.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Abnormal pinna morphology\n- Conductive hearing impairment\n- Downslanted palpebral fissures\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10243.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Short philtrum\n- Preauricular skin tag\n- Prominent nasal bridge\n- Ptosis\n- Lower eyelid coloboma\n- Short palpebral fissure\n- Bilateral choanal atresia\/stenosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BURN-MCKEOWN SYNDROME; BMKS"}],"image":"exported_images\/10244.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Thin vermilion border\n- Microcephaly\n- Impaired social interactions\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Hypertonia\n- Absent speech\n- Brisk reflexes\n- Anorexia\n- Skeletal muscle atrophy\n- CNS hypomyelination\n- Short stature\n- Decreased body weight\n- Cachexia\n- Abnormality of dental morphology\n- Prominent eyelashes\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Leukodystrophy, hypomyelinating"}],"image":"exported_images\/10245.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Dolichocephaly\n- Delayed speech and language development\n- Obesity\n- Frontal bossing\n- Delayed gross motor development\n- Depressed nasal bridge\n- Horizontal eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MACROCEPHALY\/AUTISM SYNDROME"}],"image":"exported_images\/10246.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/10247.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/10248.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MENTAL RETARDATION, AUTOSOMAL DOMINANT 57; MRD57"}],"image":"exported_images\/10249.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Deeply set eye\n- Downslanted palpebral fissures\n- Atypical behavior\n- Autistic behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Kyphoscoliosis\n- Short nose\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10250.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Downslanted palpebral fissures\n- Nystagmus\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Prominent forehead\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10251.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Nystagmus\n- Atypical behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Ventriculomegaly\n- EEG abnormality\n- Short nose\n- Aplasia\/Hypoplasia of the optic nerve\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10252.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Long face\n- Triangular face\n- Long philtrum\n- Deeply set eye\n- Downslanted palpebral fissures\n- Hypermetropia\n- Optic disc pallor\n- Autistic behavior\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10253.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Narrow mouth\n- Open mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Anteverted nares\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Ventriculomegaly\n- Chiari malformation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10254.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Downslanted palpebral fissures\n- Atypical behavior\n- Autistic behavior\n- Pectus excavatum\n- Abnormality of the metacarpal bones\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10255.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Open mouth\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Long face\n- Mandibular prognathia\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Hypermetropia\n- Blue sclerae\n- Atypical behavior\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Joint laxity\n- Exaggerated cupid's bow\n- Short nose\n- Accelerated skeletal maturation\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10256.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Myopia\n- Hypotonia\n- Dystonia\n- Absent speech\n- Atrial septal defect\n- Insomnia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/10257.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Clitoral hypoplasia\n- Abnormality of the dentition\n- Triangular mouth\n- Gingival overgrowth\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- High forehead\n- Hearing impairment\n- Anteverted nares\n- Hypermetropia\n- Impaired social interactions\n- Brachydactyly\n- Intellectual disability, mild\n- Global developmental delay\n- Frontal bossing\n- Nail dysplasia\n- Scoliosis\n- Obstructive sleep apnea\n- Mesomelia\n- Short nose\n- Broad hallux\n- Hypoplasia of the anterior nasal spine\n- Increased bone mineral density\n- Broad thumb\n- Midface retrusion\n- Abnormal labia minora morphology\n- Clinodactyly\n- Increased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/10258.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Vesicoureteral reflux\n- Bifid uvula\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ptosis\n- Proptosis\n- Shallow orbits\n- Delayed speech and language development\n- Double outlet right ventricle\n- Constipation\n- Gastroesophageal reflux\n- Gastroparesis\n- Scoliosis\n- Downturned corners of mouth\n- Inverted nipples\n- Generalized muscle weakness\n- Prominent metopic ridge\n- Atrioventricular canal defect\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10259.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Vesicoureteral reflux\n- Bifid uvula\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ptosis\n- Proptosis\n- Shallow orbits\n- Delayed speech and language development\n- Double outlet right ventricle\n- Constipation\n- Gastroesophageal reflux\n- Gastroparesis\n- Scoliosis\n- Downturned corners of mouth\n- Inverted nipples\n- Generalized muscle weakness\n- Prominent metopic ridge\n- Atrioventricular canal defect\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10260.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Vesicoureteral reflux\n- Bifid uvula\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Ptosis\n- Proptosis\n- Shallow orbits\n- Delayed speech and language development\n- Double outlet right ventricle\n- Constipation\n- Gastroesophageal reflux\n- Gastroparesis\n- Scoliosis\n- Downturned corners of mouth\n- Inverted nipples\n- Generalized muscle weakness\n- Prominent metopic ridge\n- Atrioventricular canal defect\n- Abnormal helix morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10261.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Microcephaly\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Webbed neck\n- Short neck\n- Deeply set eye\n- Delayed speech and language development\n- Brachydactyly\n- Syndactyly\n- Hypotonia\n- Intrauterine growth retardation\n- Small for gestational age\n- Sandal gap\n- Short stature\n- Flat face\n- Hypopigmented macule\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AL-RAQAD SYNDROME; ARS"}],"image":"exported_images\/10262.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Delayed speech and language development\n- Global developmental delay\n- Febrile seizure outside the age of 3 months to 6 years\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/10263.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Atypical behavior\n- Delayed speech and language development\n- Global developmental delay\n- Febrile seizure outside the age of 3 months to 6 years\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/10264.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Motor delay\n- Ventriculomegaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/10265.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Motor delay\n- Ventriculomegaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/10266.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Motor delay\n- Ventriculomegaly\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WITTEVEEN-KOLK SYNDROME; WITKOS"}],"image":"exported_images\/10267.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Cleft palate\n- Microcephaly\n- Hypertelorism\n- Hearing impairment\n- Wide nasal bridge\n- Broad nasal tip\n- Long palpebral fissure\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Hypotonia\n- Abnormal heart morphology\n- Short nail\n- Broad nail\n- Bilateral tonic-clonic seizure\n- Generalized myoclonic seizure\n- Aganglionic megacolon\n- Inability to walk\n- Ileus\n- Scoliosis\n- Elevated circulating alkaline phosphatase concentration\n- Shortening of all distal phalanges of the fingers\n- Tented upper lip vermilion\n- Chronic constipation\n- Anorectal anomaly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10268.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypertelorism\n- Anteverted nares\n- Cerebral calcification\n- Short nose\n- Depressed nasal bridge\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MARSHALL SYNDROME; MRSHS"}],"image":"exported_images\/10269.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10270.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10271.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10272.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10273.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10274.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10275.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10276.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10277.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Malar flattening\n- Coarse facial features\n- Mandibular prognathia\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Torticollis\n- Deeply set eye\n- Short attention span\n- Failure to thrive\n- Umbilical hernia\n- Bilateral tonic-clonic seizure\n- Postural instability\n- Intellectual disability, moderate\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Curly eyelashes\n- Sparse hair\n- Low hanging columella\n- Broad distal phalanx of finger\n- Broad distal phalanx of the toes\n- Dermatochalasis\n- Feeding difficulties\n- Thick vermilion border\n- Cystic acne\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10278.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Epicanthus\n- Smooth philtrum\n- Anteverted nares\n- Telecanthus\n- Prominent fingertip pads\n- Joint hypermobility\n- Joint laxity\n- Growth delay\n- Rhabdomyosarcoma\n- 2-3 toe syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/10279.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Shawl scrotum\n- Hypoplastic male external genitalia\n- Micropenis\n- Malar flattening\n- Small face\n- Triangular face\n- Micrognathia\n- Abnormal pinna morphology\n- Atresia of the external auditory canal\n- Abnormal morphology of the nasal alae\n- Prominent nose\n- Choanal stenosis\n- Downslanted palpebral fissures\n- Microphthalmia\n- Blepharophimosis\n- Iris coloboma\n- Eyelid coloboma\n- Frontal bossing\n- Preauricular skin furrow\n- Prominent metopic ridge\n- Aplasia\/Hypoplasia of the external ear\n- Narrow naris\n- Medial flaring of the eyebrow\n- obsolete Small scrotum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10280.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Shawl scrotum\n- Hypoplastic male external genitalia\n- Micropenis\n- Malar flattening\n- Small face\n- Triangular face\n- Micrognathia\n- Abnormal pinna morphology\n- Atresia of the external auditory canal\n- Abnormal morphology of the nasal alae\n- Prominent nose\n- Choanal stenosis\n- Downslanted palpebral fissures\n- Microphthalmia\n- Blepharophimosis\n- Iris coloboma\n- Eyelid coloboma\n- Frontal bossing\n- Preauricular skin furrow\n- Prominent metopic ridge\n- Aplasia\/Hypoplasia of the external ear\n- Narrow naris\n- Medial flaring of the eyebrow\n- obsolete Small scrotum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10281.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Long philtrum\n- Micrognathia\n- Underdeveloped nasal alae\n- Narrow nose\n- Microcornea\n- Myopia\n- Sparse eyelashes\n- Microdontia\n- Hyperactivity\n- Dry skin\n- Syndactyly\n- Hypotonia\n- Global developmental delay\n- Depressed nasal bridge\n- Narrow naris\n- 4-5 finger syndactyly\n- Dry hair\n- Camptodactyly\n- Short palpebral fissure\n- Esodeviation\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/10282.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Long philtrum\n- Micrognathia\n- Underdeveloped nasal alae\n- Narrow nose\n- Microcornea\n- Myopia\n- Sparse eyelashes\n- Microdontia\n- Hyperactivity\n- Dry skin\n- Syndactyly\n- Hypotonia\n- Global developmental delay\n- Depressed nasal bridge\n- Narrow naris\n- 4-5 finger syndactyly\n- Dry hair\n- Camptodactyly\n- Short palpebral fissure\n- Esodeviation\n- Narrow palpebral fissure\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/10283.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10284.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10285.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10286.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10287.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FG syndrome"}],"image":"exported_images\/10288.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10289.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/10290.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10291.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10292.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10293.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Deeply set eye\n- Abnormal repetitive mannerisms\n- Delayed speech and language development\n- Tapered finger\n- Global developmental delay\n- Broad foot\n- Ventriculomegaly\n- Unsteady gait\n- Tented upper lip vermilion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/10294.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Macrocephaly\n- Wide nasal bridge\n- Strabismus\n- Downslanted palpebral fissures\n- Telecanthus\n- Diplopia\n- Delayed speech and language development\n- Pectus excavatum\n- Tapered finger\n- Hypotonia\n- Hemiparesis\n- Pneumonia\n- Asthma\n- Delayed gross motor development\n- Unsteady gait\n- Genu valgum\n- Preauricular pit\n- Prominent nasal tip\n- Central sleep apnea\n- Weakness of facial musculature\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/10295.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/10296.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/10297.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10298.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/10299.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10300.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10301.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10302.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10303.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10304.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10305.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10306.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10307.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10308.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10309.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10310.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10311.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10312.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPEECH IMPAIRMENT AND DYSMORPHIC FACIES; NEDSID"}],"image":"exported_images\/10313.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, DYSMORPHIC FACIAL FEATURES, AND INTELLECTUAL DEVELOPMENTAL DISORDER; CHDFIDD"}],"image":"exported_images\/10314.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10315.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10316.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10317.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/10318.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEFT PALATE, CARDIAC DEFECTS, AND MENTAL RETARDATION; CPCMR"}],"image":"exported_images\/10319.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10320.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10321.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10322.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PIERPONT SYNDROME; PRPTS"}],"image":"exported_images\/10323.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME; COFG"}],"image":"exported_images\/10324.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Brachycephaly\n- Low anterior hairline\n- Hypertelorism\n- Triangular face\n- Long philtrum\n- Macrotia\n- Protruding ear\n- Prominent nasal bridge\n- Anteverted nares\n- Ptosis\n- Long palpebral fissure\n- Synophrys\n- Oligodontia\n- Short tubular bones of the hand\n- Intellectual disability\n- Seizure\n- Intellectual disability, mild\n- Global developmental delay\n- Macrodontia\n- Low posterior hairline\n- Intellectual disability, moderate\n- Delayed skeletal maturation\n- Abnormal vertebral morphology\n- Clinodactyly of the 5th finger\n- Short stature\n- Ulnar deviation of the 2nd finger\n- Small hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10325.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10326.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10327.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE; MRXSHD"}],"image":"exported_images\/10328.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10329.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Webbed neck\n- Narrow chest\n- Scoliosis\n- Shoulder muscle hypoplasia\n- Bifid nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10330.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/10331.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10332.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10333.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10334.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10335.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10336.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10337.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin vermilion border\n- Short philtrum\n- Hypoplasia of the maxilla\n- High forehead\n- Broad nasal tip\n- Downslanted palpebral fissures\n- Low hanging columella\n- Short hallux\n- Sydney crease\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CLAES-JENSEN TYPE; MRXSCJ"}],"image":"exported_images\/10338.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10339.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10340.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Thick eyebrow\n- Horizontal eyebrow\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/10341.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Long face\n- Dental crowding\n- Sparse anterior scalp hair\n- Horizontal eyebrow\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/10342.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin vermilion border\n- Retrognathia\n- Hypertelorism\n- Smooth philtrum\n- Triangular face\n- Prominent supraorbital ridges\n- Long philtrum\n- Preauricular skin tag\n- Prominent nasal bridge\n- Depressed nasal tip\n- Prominent nose\n- Ptosis\n- Thick eyebrow\n- Long palpebral fissure\n- Neurofibromas\n- Umbilical hernia\n- Highly arched eyebrow\n- Short nose\n- Preauricular pit\n- Prominent nasal tip\n- Microtia\n- Abnormal columella morphology\n- Neoplasm of the peripheral nervous system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/10343.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Broad philtrum\n- Broad forehead\n- High forehead\n- Posteriorly rotated ears\n- Ptosis\n- Hypermetropia\n- Myopia\n- Thick eyebrow\n- Delayed speech and language development\n- Decreased fetal movement\n- Polyhydramnios\n- Toe clinodactyly\n- Abnormal facial shape\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n- Thick nasal alae\n- Prominent eyelashes\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10344.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Low-set ears\n- Bulbous nose\n- Long eyelashes\n- Iris coloboma\n- Autism\n- Hyperactivity\n- Severe expressive language delay\n- Intellectual disability, severe\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/10345.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Low-set ears\n- Bulbous nose\n- Long eyelashes\n- Iris coloboma\n- Autism\n- Hyperactivity\n- Severe expressive language delay\n- Intellectual disability, severe\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/10346.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Low-set ears\n- Bulbous nose\n- Long eyelashes\n- Iris coloboma\n- Autism\n- Hyperactivity\n- Severe expressive language delay\n- Intellectual disability, severe\n- Unilateral cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/10347.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dental crowding\n- Diastema\n- Absent speech\n- Macrodontia\n- Feeding difficulties in infancy\n- Unilateral cleft palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/10348.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dental crowding\n- Diastema\n- Macrodontia\n- Intellectual disability, moderate\n- Unilateral cleft palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GLASS SYNDROME; GLASS"}],"image":"exported_images\/10349.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Epicanthus\n- Wide nasal bridge\n- Hyperactivity\n- Narrow chest\n- Hypertrichosis\n- Global developmental delay\n- Joint laxity\n- Patent ductus arteriosus\n- Bicuspid aortic valve\n- Aortic regurgitation\n- Recurrent respiratory infections\n- Tricuspid regurgitation\n- Deep palmar crease\n- Thick vermilion border\n- Impulsivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/10350.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TOLCHIN-LE CAIGNEC SYNDROME; TOLCAS"}],"image":"exported_images\/10351.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Thin upper lip vermilion\n- Hypertelorism\n- Smooth philtrum\n- Low-set ears\n- Downslanted palpebral fissures\n- Long eyelashes\n- Diastema\n- Highly arched eyebrow\n- Downturned corners of mouth\n- Prominent nasal tip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SCHUURS-HOEIJMAKERS SYNDROME; SHMS"}],"image":"exported_images\/10352.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10353.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10354.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10355.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Broad palm\n- Global developmental delay\n- Atrial septal defect\n- Elevated circulating alkaline phosphatase concentration\n- Prominent forehead\n- Thick vermilion border\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10356.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Broad palm\n- Global developmental delay\n- Atrial septal defect\n- Elevated circulating alkaline phosphatase concentration\n- Prominent forehead\n- Thick vermilion border\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10357.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Full cheeks\n- Hypertelorism\n- Long philtrum\n- Wide nasal bridge\n- Broad nasal tip\n- Upslanted palpebral fissure\n- Long palpebral fissure\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Large fleshy ears\n- Short nose\n- Bruxism\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10358.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Triangular face\n- Broad forehead\n- Narrow nose\n- Blue sclerae\n- Pectus excavatum\n- Adducted thumb\n- Hand clenching\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Joint dislocation\n- Congenital hip dislocation\n- Joint hypermobility\n- Intrauterine growth retardation\n- Umbilical hernia\n- Pes planus\n- Frontal bossing\n- Decreased body weight\n- Persistent open anterior fontanelle\n- Deep palmar crease\n- Prominent veins on trunk\n- Prematurely aged appearance\n- Palmoplantar cutis laxa\n- Lipodystrophy\n- Dermal translucency\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/10359.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Bifid uvula\n- Smooth philtrum\n- High forehead\n- Sensorineural hearing impairment\n- Choanal atresia\n- Anteverted nares\n- Downslanted palpebral fissures\n- Oligodontia\n- Delayed speech and language development\n- Prominent fingertip pads\n- Atrial septal defect\n- Gastroesophageal reflux\n- Clinodactyly of the 5th finger\n- Morphological abnormality of the semicircular canal\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10360.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10361.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10362.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Global developmental delay\n- Increased body weight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10363.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Microcephaly\n- Small face\n- Epicanthus\n- Short philtrum\n- Hearing impairment\n- Wide nose\n- Upslanted palpebral fissure\n- Short attention span\n- Global developmental delay\n- Neonatal hypotonia\n- Bruxism\n- Depressed nasal bridge\n- Tented upper lip vermilion\n- Nevus sebaceous\n- Prominent forehead\n- Head-banging\n- Self-biting\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/10364.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Microcephaly\n- Prominent occiput\n- Epicanthus\n- Narrow forehead\n- High forehead\n- Wide nasal bridge\n- Broad nasal tip\n- Anteverted nares\n- Short neck\n- Strabismus\n- Downslanted palpebral fissures\n- Dental crowding\n- Intellectual disability\n- Bilateral ptosis\n- Redundant skin\n- Fair hair\n- Short nose\n- Penile hypospadias\n- Prominent metopic ridge\n- Pes valgus\n- Feeding difficulties\n- Unilateral cryptorchidism\n- obsolete Small scrotum\n- Alveolar septal thickening\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10365.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormality of the dentition\n- Coarse facial features\n- Hearing impairment\n- Sensorineural hearing impairment\n- Strabismus\n- Myopia\n- Autism\n- obsolete Mood swings\n- Disinhibition\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Obesity\n- Hoarse voice\n- Scoliosis\n- Obstructive sleep apnea\n- Feeding difficulties in infancy\n- Skin-picking\n- Fatigue\n- Abnormal temper tantrums\n- Exophoria\n- Self-injurious behavior\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/10366.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ovarian cyst\n- Triangular face\n- Short chin\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Deeply set eye\n- Myopia\n- Rieger anomaly\n- Delayed eruption of teeth\n- Diabetes mellitus\n- Insulin resistance\n- Joint hypermobility\n- Lack of facial subcutaneous fat\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/10367.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ovarian cyst\n- Triangular face\n- Short chin\n- Micrognathia\n- Low-set ears\n- Underdeveloped nasal alae\n- Deeply set eye\n- Myopia\n- Rieger anomaly\n- Delayed eruption of teeth\n- Diabetes mellitus\n- Insulin resistance\n- Joint hypermobility\n- Lack of facial subcutaneous fat\n- Prominent forehead\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT SYNDROME"}],"image":"exported_images\/10368.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Recurrent respiratory infections\n- Curved phalanges of the hand\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10369.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Compulsive behaviors\n- Delayed speech and language development\n- Hypotonia\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Pes planus\n- Sleep disturbance\n- Talipes valgus\n- Attention deficit hyperactivity disorder\n- Dust mite allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/10370.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Compulsive behaviors\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability\n- Hypotonia\n- Dysarthria\n- Global developmental delay\n- Motor delay\n- Abnormal number of teeth\n- Attention deficit hyperactivity disorder\n- Bipolar affective disorder\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/10371.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/10372.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/10373.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, IMPAIRED GROWTH, DYSMORPHIC FACIES, AND AXONAL NEUROPATHY; DIGFAN"}],"image":"exported_images\/10374.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10375.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VERHEIJ SYNDROME; VRJS"}],"image":"exported_images\/10376.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Pontocerebellar hypoplasia"}],"image":"exported_images\/10377.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS; IDDSSAD"}],"image":"exported_images\/10378.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/10379.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MICROCEPHALY WITH OR WITHOUT CHORIORETINOPATHY, LYMPHEDEMA, OR MENTAL RETARDATION; MCLMR"}],"image":"exported_images\/10380.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10381.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10382.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10383.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10384.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10385.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HELSMOORTEL-VAN DER AA SYNDROME; HVDAS"}],"image":"exported_images\/10386.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES; NEDLBA"}],"image":"exported_images\/10387.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10388.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micrognathia\n- Atresia of the external auditory canal\n- Downslanted palpebral fissures\n- Eyelid coloboma\n- Microtia\n- Aplasia\/Hypoplasia of the middle ear\n- Hypoplasia of the zygomatic bone\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10389.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10390.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10391.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Baraitser-Winter syndrome"}],"image":"exported_images\/10392.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10393.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10394.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10395.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10396.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10397.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10398.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10399.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10400.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10401.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10402.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10403.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10404.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10405.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10406.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10407.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10408.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEAVER SYNDROME; WVS"}],"image":"exported_images\/10409.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/10410.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/10411.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/10412.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OCULODENTODIGITAL DYSPLASIA; ODDD"}],"image":"exported_images\/10413.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Long eyelashes\n- Upslanted palpebral fissure\n- Autistic behavior\n- Phimosis\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Limited pronation\/supination of forearm\n- Sparse hair\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/10414.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Long face\n- Mandibular prognathia\n- Microretrognathia\n- Triangular face\n- Abnormal pinna morphology\n- Macrotia\n- Protruding ear\n- Prominent nose\n- Long eyelashes\n- Upslanted palpebral fissure\n- Autistic behavior\n- Phimosis\n- Coarse hair\n- Intellectual disability, moderate\n- Skeletal muscle atrophy\n- Limited pronation\/supination of forearm\n- Sparse hair\n- Ankylosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/10415.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Facial hypotonia\n- Hypertelorism\n- Hearing impairment\n- Atypical behavior\n- Abnormality of the skin\n- Joint laxity\n- Hypoplasia of the corpus callosum\n- Intellectual disability, severe\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/10416.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Broad forehead\n- High forehead\n- Narrow nose\n- Anteverted nares\n- Atypical behavior\n- Hypotonia\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/10417.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Visual impairment\n- Atypical behavior\n- Hypotonia\n- Intellectual disability, severe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNIJDERS BLOK TYPE; MRXSSB"}],"image":"exported_images\/10418.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Everted lower lip vermilion\n- Hypertelorism\n- Wide nose\n- Anteverted nares\n- Tapered finger\n- Global developmental delay\n- Intellectual disability, moderate\n- Everted upper lip vermilion\n- Thick vermilion border\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/10419.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Hypodontia\n- Abnormality of the nervous system\n- Delayed speech and language development\n- Pectus carinatum\n- Global developmental delay\n- Failure to thrive\n- Small for gestational age\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Scoliosis\n- Short stature\n- Atonic seizure\n- Thick vermilion border\n- Short palpebral fissure\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/10420.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Ptosis\n- Hypodontia\n- Abnormality of the nervous system\n- Delayed speech and language development\n- Pectus carinatum\n- Global developmental delay\n- Failure to thrive\n- Small for gestational age\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Scoliosis\n- Short stature\n- Atonic seizure\n- Thick vermilion border\n- Short palpebral fissure\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COFFIN-LOWRY SYNDROME; CLS"}],"image":"exported_images\/10421.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia minora\n- Narrow mouth\n- High palate\n- Microcephaly\n- Wide anterior fontanel\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Underdeveloped nasal alae\n- Choanal atresia\n- Proptosis\n- Hemangioma\n- Prominent scalp veins\n- Global developmental delay\n- Cerebellar hypoplasia\n- Communicating hydrocephalus\n- Failure to thrive\n- Small for gestational age\n- Bicuspid aortic valve\n- Secundum atrial septal defect\n- Short toe\n- Pulmonary arterial hypertension\n- Ventriculomegaly\n- Birth length less than 3rd percentile\n- Shoulder subluxation\n- Short stature\n- Decreased body weight\n- Widely patent fontanelles and sutures\n- Hypoplastic nasal bridge\n- Lateral ventricle dilatation\n- Severe intrauterine growth retardation\n- Axial hypotonia\n- Ulnar deviation of finger\n- Contracture of the distal interphalangeal joint of the fingers\n- Increased nuchal translucency\n- Echogenic fetal bowel\n- Prominent forehead\n- Midface retrusion\n- Feeding difficulties\n- Short palpebral fissure\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hutchinson-Gilford progeria"}],"image":"exported_images\/10422.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/10423.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Brachycephaly\n- Microcephaly\n- Malar flattening\n- Small face\n- Long face\n- Mandibular prognathia\n- Macrotia\n- Protruding ear\n- Acne\n- Hip dysplasia\n- Slender build\n- Intellectual disability, moderate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RENPENNING SYNDROME 1; RENS1"}],"image":"exported_images\/10424.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Thin vermilion border\n- Epicanthus\n- Facial asymmetry\n- Cupped ear\n- Facial erythema\n- Growth delay\n- Alopecia\n- Short stature\n- Dermal atrophy\n- 2-3 toe cutaneous syndactyly\n- Nail dystrophy\n- Short 2nd finger\n- Intracranial cystic lesion\n- Asymmetry of the ears\n- Distributed along Blaschko lines\n- Clinodactyly of the 3rd finger\n- Telangiectasia of the skin\n- Acute respiratory distress syndrome\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/10425.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Microcornea\n- Strabismus\n- Coloboma\n- Hypopigmentation of the skin\n- Syndactyly\n- Sandal gap\n- Intellectual disability, moderate\n- Thoracolumbar scoliosis\n- Disproportionate short stature\n- Dermal atrophy\n- Intermittent generalized erythematous papular rash\n- Oligodactyly\n- Distributed along Blaschko lines\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FOCAL DERMAL HYPOPLASIA; FDH"}],"image":"exported_images\/10426.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Cholelithiasis\n- Cholecystitis\n- Cholestasis\n- Recurrent skin infections\n- Cardiomyopathy\n- Pancreatitis\n- Recurrent fever\n- Pneumonia\n- Gastrointestinal hemorrhage\n- Infectious encephalitis\n- Conjugated hyperbilirubinemia\n- Elevated circulating alkaline phosphatase concentration\n- Decreased circulating antibody level\n- Chronic bronchitis\n- Combined immunodeficiency\n- Chronic pulmonary obstruction\n- Chronic sinusitis\n- Recurrent acute respiratory tract infection\n- Hepatitis\n- Cryptococcal meningitis\n- Granuloma\n- Vasculitis in the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/10427.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Cholelithiasis\n- Cholecystitis\n- Cholestasis\n- Recurrent skin infections\n- Cardiomyopathy\n- Pancreatitis\n- Recurrent fever\n- Pneumonia\n- Gastrointestinal hemorrhage\n- Infectious encephalitis\n- Conjugated hyperbilirubinemia\n- Elevated circulating alkaline phosphatase concentration\n- Decreased circulating antibody level\n- Chronic bronchitis\n- Combined immunodeficiency\n- Chronic pulmonary obstruction\n- Chronic sinusitis\n- Recurrent acute respiratory tract infection\n- Hepatitis\n- Cryptococcal meningitis\n- Granuloma\n- Vasculitis in the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/10428.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertension\n- Cholelithiasis\n- Cholecystitis\n- Cholestasis\n- Recurrent skin infections\n- Cardiomyopathy\n- Pancreatitis\n- Recurrent fever\n- Pneumonia\n- Gastrointestinal hemorrhage\n- Infectious encephalitis\n- Conjugated hyperbilirubinemia\n- Elevated circulating alkaline phosphatase concentration\n- Decreased circulating antibody level\n- Chronic bronchitis\n- Combined immunodeficiency\n- Chronic pulmonary obstruction\n- Chronic sinusitis\n- Recurrent acute respiratory tract infection\n- Hepatitis\n- Cryptococcal meningitis\n- Granuloma\n- Vasculitis in the skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NIJMEGEN BREAKAGE SYNDROME; NBS"}],"image":"exported_images\/10429.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- High palate\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Highly arched eyebrow\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10430.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Cryptorchidism\n- Microcephaly\n- Low-set ears\n- Downslanted palpebral fissures\n- Intellectual disability\n- Short stature\n- Low hanging columella\n- Broad hallux\n- Broad thumb\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10431.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Convex nasal ridge\n- Intellectual disability\n- Broad hallux\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10432.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Blepharophimosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/10433.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Epicanthus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS; BPES"}],"image":"exported_images\/10434.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Bulbous nose\n- Deeply set eye\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10435.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Pointed chin\n- Triangular face\n- Wide nasal bridge\n- Tapered finger\n- Global developmental delay\n- Specific learning disability\n- Growth delay\n- Small for gestational age\n- Short toe\n- Gastroesophageal reflux\n- Elevated circulating thyroid-stimulating hormone concentration\n- Butterfly vertebrae\n- Short finger\n- Prominent forehead\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10436.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the nose\n- Microphthalmia\n- Aplasia of the nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOSMA ARHINIA MICROPHTHALMIA SYNDROME; BAMS"}],"image":"exported_images\/10437.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Hypertelorism\n- Progressive sensorineural hearing impairment\n- Mixed hearing impairment\n- Abnormality of the lower limb\n- Absence of acoustic reflex\n- Flat face\n- Abnormality of the tympanic membrane\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/10438.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Dysostosis multiplex\n- Thickened skin\n- Global developmental delay\n- Umbilical hernia\n- Congestive heart failure\n- Cardiomegaly\n- Hepatomegaly\n- Elbow flexion contracture\n- Disproportionate short-trunk short stature\n- Knee flexion contracture\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/10439.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Coarse facial features\n- Dysostosis multiplex\n- Thickened skin\n- Global developmental delay\n- Umbilical hernia\n- Congestive heart failure\n- Cardiomegaly\n- Hepatomegaly\n- Elbow flexion contracture\n- Disproportionate short-trunk short stature\n- Knee flexion contracture\n- Flexion contracture of finger\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/10440.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Gingival overgrowth\n- Coarse facial features\n- Full cheeks\n- Shallow orbits\n- Prominent superficial veins\n- Thickened skin\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Flat face\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/10441.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Conductive hearing impairment\n- Intellectual disability\n- Mitral regurgitation\n- Aortic regurgitation\n- Bone pain\n- Arthralgia\n- Obstructive sleep apnea\n- Spinal canal stenosis\n- Central sleep apnea\n- Systolic heart murmur\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/10442.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Dysostosis multiplex\n- Abnormal aortic valve morphology\n- Aortic regurgitation\n- Increased serum beta-hexosaminidase\n- Short stature\n- Decreased body weight\n- Flattened moderately deformed vertebrae\n- Limited interphalangeal movement\n- Metacarpophalangeal joint contracture\n- Short distal phalanx of finger\n- Systolic heart murmur\n- Hand pain\n- Ectrodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MUCOLIPIDOSIS II ALPHA\/BETA"}],"image":"exported_images\/10443.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n- Limitation of joint mobility\n- Mitral regurgitation\n- Aortic regurgitation\n- Limited shoulder movement\n- Corneal opacity\n- Limited hip movement\n- Limitation of knee mobility\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10444.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n- Gingivitis\n- Macrocephaly\n- Coarse facial features\n- Wide nasal bridge\n- Exotropia\n- Dysostosis multiplex\n- Intellectual disability\n- Limitation of joint mobility\n- Joint stiffness\n- Hepatosplenomegaly\n- Umbilical hernia\n- Meckel diverticulum\n- Short stature\n- Lower thoracic kyphosis\n- Corneal opacity\n- Respiratory tract infection\n- Thick vermilion border\n- Flexion contracture of finger\n- Systolic heart murmur\n- Purulent rhinitis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10445.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macroglossia\n- Coarse facial features\n- Hearing impairment\n- Delayed speech and language development\n- Abnormality of the skeletal system\n- Hypertrichosis\n- Broad finger\n- Umbilical hernia\n- Hepatomegaly\n- Limited elbow movement\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10446.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macrocephaly\n- Coarse facial features\n- Otitis media\n- Abnormality of the skeletal system\n- Thickened skin\n- Umbilical hernia\n- Abnormal heart morphology\n- Ventricular septal defect\n- Mitral regurgitation\n- Hepatomegaly\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Kyphosis\n- Mesomelia\n- Mucopolysacchariduria\n- Severe global developmental delay\n- Dilation of Virchow-Robin spaces\n- Stiff elbow\n- Overweight\n- Abnormal circulating hyaluronic acid concentration\n- Increased size of nasopharyngeal adenoids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10447.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10448.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Sensorineural hearing impairment\n- Umbilical hernia\n- Abnormal mitral valve morphology\n- Abnormal aortic valve morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10449.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Thick lower lip vermilion\n- Microcephaly\n- Coarse facial features\n- Broad philtrum\n- Low anterior hairline\n- Mandibular prognathia\n- Long philtrum\n- Narrow nasal bridge\n- Anteverted nares\n- Downslanted palpebral fissures\n- Widely spaced teeth\n- Prominent fingertip pads\n- Seizure\n- Short toe\n- Scoliosis\n- Generalized amyotrophy\n- Short stature\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Microtia\n- Short phalanx of finger\n- Thick nasal alae\n- Short metacarpal\n- Short metatarsal\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10450.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Cryptorchidism\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Low anterior hairline\n- Triangular face\n- Long philtrum\n- Anteverted nares\n- Downslanted palpebral fissures\n- Periorbital wrinkles\n- Widely spaced teeth\n- Prominent fingertip pads\n- Seizure\n- Absent speech\n- Small for gestational age\n- Umbilical hernia\n- Short toe\n- Delayed skeletal maturation\n- Short stature\n- Prominent interphalangeal joints\n- Excessive wrinkled skin\n- Sparse hair\n- Short phalanx of finger\n- Thick nasal alae\n- Short metacarpal\n- Intellectual disability, severe\n- Severe global developmental delay\n- Wide nasal base\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10451.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Inguinal hernia\n- Wide mouth\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Coarse facial features\n- Long philtrum\n- Abnormal pinna morphology\n- Wide nose\n- Anteverted nares\n- Ptosis\n- Long eyelashes\n- Thick eyebrow\n- Hyperactivity\n- Hirsutism\n- Intellectual disability\n- Seizure\n- Umbilical hernia\n- Sandal gap\n- Sparse scalp hair\n- Depressed nasal bridge\n- Prominent interphalangeal joints\n- Aplasia\/Hypoplasia of the distal phalanx of the 5th finger\n- Abnormal distal phalanx morphology of finger\n- Thick nasal alae\n- Short metacarpal\n- Short metatarsal\n- Feeding difficulties\n- Noncompaction cardiomyopathy\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10452.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Hearing impairment\n- Recurrent otitis media\n- Broad nasal tip\n- Thick eyebrow\n- Hyperorality\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Scoliosis\n- Short stature\n- Prominent interphalangeal joints\n- Feeding difficulties in infancy\n- Pineal cyst\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10453.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Hearing impairment\n- Recurrent otitis media\n- Broad nasal tip\n- Thick eyebrow\n- Hyperorality\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Scoliosis\n- Short stature\n- Prominent interphalangeal joints\n- Feeding difficulties in infancy\n- Pineal cyst\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10454.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Thin upper lip vermilion\n- Microcephaly\n- Hearing impairment\n- Recurrent otitis media\n- Broad nasal tip\n- Thick eyebrow\n- Hyperorality\n- Delayed speech and language development\n- Seizure\n- Hypotonia\n- Global developmental delay\n- Absent speech\n- Scoliosis\n- Short stature\n- Prominent interphalangeal joints\n- Feeding difficulties in infancy\n- Pineal cyst\n- Arachnoid cyst\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NICOLAIDES-BARAITSER SYNDROME; NCBRS"}],"image":"exported_images\/10455.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Retrognathia\n- Long philtrum\n- Anteverted nares\n- Short nose\n- Concave nasal ridge\n- Flat face\n- Short palpebral fissure\n- High insertion of columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10456.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10457.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10458.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10459.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10460.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10461.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Narrow forehead\n- Micrognathia\n- Anteverted nares\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10462.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Labial hypoplasia\n- Microcephaly\n- Recurrent otitis media\n- Anteverted nares\n- Short neck\n- Broad neck\n- Strabismus\n- Cataract\n- Developmental cataract\n- Single transverse palmar crease\n- Cutis laxa\n- Skin rash\n- Cutaneous photosensitivity\n- Hypotonia\n- Failure to thrive\n- Patent ductus arteriosus\n- Hammertoe\n- Vomiting\n- Gastroesophageal reflux\n- Poor suck\n- Abnormal cortical gyration\n- High, narrow palate\n- Elevated hepatic transaminase\n- Hypocholesterolemia\n- Short nose\n- 2-3 toe syndactyly\n- Wide intermamillary distance\n- Edema of the dorsum of hands\n- Moderate global developmental delay\n- Short corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10463.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cleft palate\n- High palate\n- Microcephaly\n- Narrow forehead\n- Otitis media\n- Anteverted nares\n- Cataract\n- Irritability\n- Narrow chest\n- Skin rash\n- Cutaneous photosensitivity\n- Seizure\n- Severe failure to thrive\n- Gastroesophageal reflux\n- Ventriculomegaly\n- Low-set nipples\n- Obstructive sleep apnea\n- 2-3 toe syndactyly\n- Ulnar deviation of finger\n- Short thumb\n- Abnormality of the palmar creases\n- Recurrent sinusitis\n- Moderate global developmental delay\n- Delayed myelination\n- Auditory sensitivity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10464.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10465.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10466.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10467.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10468.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Microcephaly\n- Short chin\n- High forehead\n- Wide nasal bridge\n- Ptosis\n- Short stature\n- 2-3 toe syndactyly\n- Short finger\n- Abnormality of the palmar creases\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-LEMLI-OPITZ SYNDROME; SLOS"}],"image":"exported_images\/10469.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10470.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10471.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10472.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10473.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10474.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10475.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10476.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10477.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10478.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10479.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10480.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10481.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10482.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/10483.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/10484.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Micropenis\n- Intellectual disability\n- Kyphosis\n- Abdominal obesity\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC"}],"image":"exported_images\/10485.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Wide mouth\n- Periorbital fullness\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10486.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WILLIAMS-BEUREN SYNDROME; WBS"}],"image":"exported_images\/10487.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Micropenis\n- Wide mouth\n- Hypertelorism\n- Underdeveloped nasal alae\n- Short neck\n- Broad neck\n- Upslanted palpebral fissure\n- Synophrys\n- Dry skin\n- Pes cavus\n- Short foot\n- Low posterior hairline\n- Generalized hirsutism\n- Hyperbilirubinemia\n- Depressed nasal bridge\n- Wide intermamillary distance\n- Nail dystrophy\n- Low hanging columella\n- Abnormal hair whorl\n- Intellectual disability, severe\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, NASCIMENTO TYPE; MRXSN"}],"image":"exported_images\/10488.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10489.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10490.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Ptosis\n- Intellectual disability, mild\n- Intrauterine growth retardation\n- Atrial septal defect\n- Pulmonic stenosis\n- Short foot\n- Clinodactyly of the 5th finger\n- Short palm\n- 2-3 toe syndactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10491.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Astigmatism\n- Intrauterine growth retardation\n- Intellectual disability, severe\n- Nasogastric tube feeding in infancy\n- Corneal ulceration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10492.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Astigmatism\n- Intrauterine growth retardation\n- Intellectual disability, severe\n- Nasogastric tube feeding in infancy\n- Corneal ulceration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10493.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Hearing impairment\n- Wide nasal bridge\n- Widely spaced teeth\n- Ocular albinism\n- Hypotonia\n- Spasticity\n- Absent speech\n- Pneumonia\n- Preauricular pit\n- Depressed nasal bridge\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 40; MRD40"}],"image":"exported_images\/10494.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Smooth philtrum\n- Prominent nasal bridge\n- Wide nasal bridge\n- Thickened nuchal skin fold\n- Retinal coloboma\n- Coloboma\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Abnormal cerebellum morphology\n- Cerebellar hypoplasia\n- Absent speech\n- Abnormal heart morphology\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Hypoplasia of the corpus callosum\n- Hypoplasia of the brainstem\n- Downturned corners of mouth\n- Redundant neck skin\n- Wide intermamillary distance\n- Abnormality of the palmar creases\n- Prominent forehead\n- Enlarged thalamic volume\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROOCULOCARDIOGENITOURINARY SYNDROME; NOCGUS"}],"image":"exported_images\/10495.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Cryptorchidism\n- Vesicoureteral reflux\n- Hydronephrosis\n- Open mouth\n- High palate\n- Turricephaly\n- Long face\n- Thickened helices\n- Megalocornea\n- Ptosis\n- Hypermetropia\n- Long palpebral fissure\n- Delayed speech and language development\n- Pectus excavatum\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Bicuspid aortic valve\n- Overlapping toe\n- Vomiting\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Migraine\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Gastroparesis\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Inverted nipples\n- Cleft ala nasi\n- Vertebral segmentation defect\n- CNS hypomyelination\n- Intestinal pseudo-obstruction\n- Aortic aneurysm\n- Sparse lateral eyebrow\n- Prominent metopic ridge\n- Agenesis of incisor\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Hypoplastic helices\n- Bifid tongue\n- Polydactyly\n- Agenesis of molar\n- Wide nasal ridge\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10496.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Cryptorchidism\n- Vesicoureteral reflux\n- Hydronephrosis\n- Open mouth\n- High palate\n- Turricephaly\n- Long face\n- Thickened helices\n- Megalocornea\n- Ptosis\n- Hypermetropia\n- Long palpebral fissure\n- Delayed speech and language development\n- Pectus excavatum\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Bicuspid aortic valve\n- Overlapping toe\n- Vomiting\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Migraine\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Gastroparesis\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Inverted nipples\n- Cleft ala nasi\n- Vertebral segmentation defect\n- CNS hypomyelination\n- Intestinal pseudo-obstruction\n- Aortic aneurysm\n- Sparse lateral eyebrow\n- Prominent metopic ridge\n- Agenesis of incisor\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Hypoplastic helices\n- Bifid tongue\n- Polydactyly\n- Agenesis of molar\n- Wide nasal ridge\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10497.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Cryptorchidism\n- Vesicoureteral reflux\n- Hydronephrosis\n- Open mouth\n- High palate\n- Turricephaly\n- Long face\n- Thickened helices\n- Megalocornea\n- Ptosis\n- Hypermetropia\n- Long palpebral fissure\n- Delayed speech and language development\n- Pectus excavatum\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Bicuspid aortic valve\n- Overlapping toe\n- Vomiting\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Migraine\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Gastroparesis\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Inverted nipples\n- Cleft ala nasi\n- Vertebral segmentation defect\n- CNS hypomyelination\n- Intestinal pseudo-obstruction\n- Aortic aneurysm\n- Sparse lateral eyebrow\n- Prominent metopic ridge\n- Agenesis of incisor\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Hypoplastic helices\n- Bifid tongue\n- Polydactyly\n- Agenesis of molar\n- Wide nasal ridge\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10498.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Coarse facial features\n- Hypertelorism\n- Bulbous nose\n- Synophrys\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Abnormal rib morphology\n- Abnormality of the vertebral column\n- Abnormality of the hand\n- Macrodontia\n- Abnormal facial shape\n- Low posterior hairline\n- Coarse hair\n- Exaggerated cupid's bow\n- Intellectual disability, moderate\n- Scoliosis\n- Clinodactyly of the 5th finger\n- Bilateral single transverse palmar creases\n- Short 5th finger\n- Unilateral cryptorchidism\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10499.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3-Methylglutaconic aciduria"}],"image":"exported_images\/10500.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Brachycephaly\n- Coarse facial features\n- Low anterior hairline\n- Hypertelorism\n- Short philtrum\n- Small forehead\n- Macrotia\n- Convex nasal ridge\n- Short neck\n- Long eyelashes\n- Thick eyebrow\n- Aggressive behavior\n- Delayed speech and language development\n- Hypertrichosis\n- Global developmental delay\n- Joint laxity\n- Obesity\n- Short foot\n- Short toe\n- Intellectual disability, moderate\n- Poor head control\n- Expressive language delay\n- Genu valgum\n- Poor hand-eye coordination\n- Anterior pituitary hypoplasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES; IDDFBA"}],"image":"exported_images\/10501.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BAINBRIDGE-ROPERS SYNDROME; BRPS"}],"image":"exported_images\/10502.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Glossoptosis\n- Wide anterior fontanel\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Proptosis\n- Myopia\n- Optic atrophy\n- Synophrys\n- Abnormality of the vertebral column\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Tracheomalacia\n- Short nose\n- Short stature\n- Cervical C2\/C3 vertebral fusion\n- Aspiration pneumonia\n- Bronchitis\n- Unilateral cryptorchidism\n- Hip subluxation\n- Sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/10503.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES; IDDALDS"}],"image":"exported_images\/10504.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/10505.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEBALID SYNDROME; CEBALID"}],"image":"exported_images\/10506.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Silver-Russell syndrome"}],"image":"exported_images\/10507.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Treacher Collins syndrome"}],"image":"exported_images\/10508.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GNAI1"}],"image":"exported_images\/10509.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/10510.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/10511.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 50, WITH BEHAVIORAL ABNORMALITIES; MRD50"}],"image":"exported_images\/10512.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/10513.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRIMROSE SYNDROME; PRIMS"}],"image":"exported_images\/10514.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/10515.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/10516.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ARBOLEDA-THAM SYNDROME; ARTHS"}],"image":"exported_images\/10517.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rothmund-Thomson syndrome"}],"image":"exported_images\/10518.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Meier-Gorlin syndrome"}],"image":"exported_images\/10519.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Microcephaly\n- Facial grimacing\n- Dental crowding\n- Abnormal fingertip morphology\n- Growth delay\n- Intellectual disability, moderate\n- High, narrow palate\n- Bilateral cryptorchidism\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10520.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/10521.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/10522.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 21; MRD21"}],"image":"exported_images\/10523.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES; NEDDFSA"}],"image":"exported_images\/10524.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Opitz GBBB syndrome"}],"image":"exported_images\/10525.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/10526.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TATTON-BROWN-RAHMAN SYNDROME; TBRS"}],"image":"exported_images\/10527.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES; NEDHIB"}],"image":"exported_images\/10528.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10529.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BASILICATA-AKHTAR SYNDROME; MRXSBA"}],"image":"exported_images\/10530.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long philtrum\n- Telecanthus\n- Spatulate thumbs\n- Joint laxity\n- Bilateral talipes equinovarus\n- Scoliosis\n- Hip dislocation\n- Short stature\n- 2-3 toe syndactyly\n- Knee dislocation\n- Bilateral elbow dislocations\n- Depressed nasal bridge\n- Prominent forehead\n- Broad fingertip\n- Midface retrusion\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LARSEN SYNDROME; LRS"}],"image":"exported_images\/10531.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SEIZURES, AND DISTAL LIMB ANOMALIES; IDDFSDA"}],"image":"exported_images\/10532.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10533.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10534.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10535.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10536.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Anteverted nares\n- Downslanted palpebral fissures\n- Motor delay\n- Intellectual disability, severe\n- Moderate global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 33; MRXS33"}],"image":"exported_images\/10537.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/10538.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SMITH-MAGENIS SYNDROME; SMS"}],"image":"exported_images\/10539.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/10540.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/10541.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RETT SYNDROME; RTT"}],"image":"exported_images\/10542.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/10543.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/10544.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Dolichocephaly\n- Hypertelorism\n- Narrow forehead\n- Low-set ears\n- Thickened helices\n- Strabismus\n- Shield chest\n- Numerous nevi\n- Intellectual disability\n- Hypotonia\n- Joint hypermobility\n- Dysphagia\n- Poor suck\n- Cubitus valgus\n- Short stature\n- Depressed nasal bridge\n- Prominent forehead\n- Tube feeding\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10545.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/10546.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/10547.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/10548.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, LUBS TYPE; MRXSL"}],"image":"exported_images\/10549.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10550.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10551.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10552.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10553.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10554.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PITT-HOPKINS SYNDROME; PTHS"}],"image":"exported_images\/10555.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10556.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10557.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10558.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10559.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10560.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10561.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10562.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10563.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10564.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COSTELLO SYNDROME; CSTLO"}],"image":"exported_images\/10565.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10566.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10567.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10568.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10569.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/10570.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/10571.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/10572.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Bardet-Biedl syndrome"}],"image":"exported_images\/10573.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10574.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10575.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10576.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10577.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10578.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10579.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10580.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kleefstra syndrome"}],"image":"exported_images\/10581.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/10582.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Stickler syndrome"}],"image":"exported_images\/10583.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/10584.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/10585.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CANTU SYNDROME"}],"image":"exported_images\/10586.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SANDESTIG-STEFANOVA SYNDROME; SANDSTEF"}],"image":"exported_images\/10587.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/10588.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/10589.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/10590.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1"}],"image":"exported_images\/10591.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 83; DEE83"}],"image":"exported_images\/10592.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME; ACOGS"}],"image":"exported_images\/10593.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10594.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10595.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10596.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10597.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10598.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10599.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10600.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10601.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10602.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10603.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Full cheeks\n- Abnormality of the chin\n- Wide nasal bridge\n- Thick eyebrow\n- Delayed speech and language development\n- Global developmental delay\n- Neonatal hypotonia\n- Dystonia\n- Myoclonus\n- Absent speech\n- Slender build\n- Broad-based gait\n- Drooling\n- Highly arched eyebrow\n- Episodic vomiting\n- Scoliosis\n- Rhabdomyolysis\n- Long eyebrows\n- Prominent nasal tip\n- Feeding difficulties in infancy\n- Caesarian section\n- Tented philtrum\n- Self-biting\n- Heart murmur\n- Abnormal sweat homeostasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10604.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10605.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10606.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10607.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10608.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/10609.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALSTROM SYNDROME; ALMS"}],"image":"exported_images\/10610.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Fraser syndrome"}],"image":"exported_images\/10611.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10612.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/10613.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/10614.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10615.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10616.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10617.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BEAULIEU-BOYCOTT-INNES SYNDROME; BBIS"}],"image":"exported_images\/10618.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALZAHRANI-KUWAHARA SYNDROME; ALKUS"}],"image":"exported_images\/10619.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10620.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10621.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/10622.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/10623.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAND SYNDROME; GAND"}],"image":"exported_images\/10624.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AYME-GRIPP SYNDROME; AYGRP"}],"image":"exported_images\/10625.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALAZAMI SYNDROME; ALAZS"}],"image":"exported_images\/10626.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10627.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SNIJDERS BLOK-CAMPEAU SYNDROME; SNIBCPS"}],"image":"exported_images\/10628.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/10629.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LUSCAN-LUMISH SYNDROME; LLS"}],"image":"exported_images\/10630.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Protruding ear\n- Bulbous nose\n- Synophrys\n- Delayed speech and language development\n- Brachydactyly\n- Seizure\n- Motor delay\n- Deep philtrum\n- Long eyebrows\n- Broad eyebrow\n- Anteverted ears\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10631.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/10632.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Multiple congenital anomalies-hypotonia-seizures syndrome"}],"image":"exported_images\/10633.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/10634.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/10635.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10636.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/10637.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10638.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10639.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10640.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10641.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10642.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10643.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10644.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10645.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10646.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10647.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10648.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10649.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10650.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10651.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10652.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10653.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10654.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10655.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Microcephaly\n- Broad philtrum\n- Astigmatism\n- Thick eyebrow\n- Atypical behavior\n- Acne\n- Global developmental delay\n- Incoordination\n- Cerebral visual impairment\n- Body odor\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10656.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93"}],"image":"exported_images\/10657.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HYPOPARATHYROIDISM-RETARDATION-DYSMORPHISM SYNDROME; HRDS"}],"image":"exported_images\/10658.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BRANCHIOOCULOFACIAL SYNDROME; BOFS"}],"image":"exported_images\/10659.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Craniosynostosis"}],"image":"exported_images\/10660.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/10661.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ROBIN SEQUENCE WITH CLEFT MANDIBLE AND LIMB ANOMALIES"}],"image":"exported_images\/10662.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin vermilion border\n- Low anterior hairline\n- Short philtrum\n- Triangular face\n- Low-set ears\n- Abnormal pinna morphology\n- Small earlobe\n- Narrow nasal bridge\n- Deeply set eye\n- Long eyelashes\n- Dental malocclusion\n- Microdontia\n- Aggressive behavior\n- Delayed speech and language development\n- Brachydactyly\n- Intellectual disability, mild\n- Failure to thrive\n- Recurrent respiratory infections\n- Expressive language delay\n- Hyperkinetic movements\n- Long nose\n- Short stature\n- Short humerus\n- Attention deficit hyperactivity disorder\n- Feeding difficulties in infancy\n- Broad fingertip\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10663.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/10664.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/10665.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/10666.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FACIAL PALSY, CONGENITAL, WITH PTOSIS AND VELOPHARYNGEAL DYSFUNCTION; FPVEPD"}],"image":"exported_images\/10667.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10668.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10669.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOEBIUS SYNDROME; MBS"}],"image":"exported_images\/10670.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/10671.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/10672.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/10673.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/10674.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"3MC syndrome"}],"image":"exported_images\/10675.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- High palate\n- Epicanthus\n- Micrognathia\n- Abnormal nasal tip morphology\n- Upslanted palpebral fissure\n- Delayed speech and language development\n- Motor delay\n- Microtia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL LIMB ANOMALIES; NEDDFL"}],"image":"exported_images\/10676.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cold-induced sweating syndrome"}],"image":"exported_images\/10677.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/10678.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Ehlers-Danlos syndrome"}],"image":"exported_images\/10679.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10680.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Long QT syndrome"}],"image":"exported_images\/10681.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JANSEN-DE VRIES SYNDROME; JDVS"}],"image":"exported_images\/10682.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microcephaly, primary"}],"image":"exported_images\/10683.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10684.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10685.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10686.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Thin vermilion border\n- Microcephaly\n- Abnormality of the philtrum\n- Hypertelorism\n- Triangular face\n- Bulbous nose\n- Prominent nasal bridge\n- Prominent nose\n- Anteverted nares\n- Synophrys\n- Intellectual disability\n- Global developmental delay\n- Abnormal heart morphology\n- Exaggerated cupid's bow\n- Sleep disturbance\n- Thick nasal alae\n- Long upper lip\n- Prominence of the zygomatic bone\n- Wide nasal base\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10687.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10688.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10689.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10690.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10691.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10692.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Wide nasal bridge\n- Esotropia\n- Delayed speech and language development\n- Global developmental delay\n- Generalized hypotonia\n- Macrodontia\n- Delayed gross motor development\n- Feeding difficulties in infancy\n- Tented philtrum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10693.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Galloway-Mowat syndrome"}],"image":"exported_images\/10694.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10695.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10696.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10697.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/10698.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 7; MRD7"}],"image":"exported_images\/10699.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTOPALATODIGITAL SYNDROME, TYPE I; OPD1"}],"image":"exported_images\/10700.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Frontometaphyseal dysplasia"}],"image":"exported_images\/10701.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10702.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10703.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10704.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10705.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10706.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10707.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10708.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10709.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10710.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/10711.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/10712.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/10713.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/10714.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ACROMICRIC DYSPLASIA; ACMICD"}],"image":"exported_images\/10715.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SPASTIC DIPLEGIA AND VISUAL DEFECTS; NEDSDV"}],"image":"exported_images\/10716.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Smooth philtrum\n- Broad forehead\n- Long eyelashes\n- Delayed speech and language development\n- Global developmental delay\n- Gait disturbance\n- Bradycardia\n- Apnea\n- Abnormality of temperature regulation\n- Generalized neonatal hypotonia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10717.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"IMPAIRED INTELLECTUAL DEVELOPMENT AND DISTINCTIVE FACIAL FEATURES WITH OR WITHOUT CARDIAC DEFECTS; MRFACD"}],"image":"exported_images\/10718.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10719.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10720.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10721.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Thin upper lip vermilion\n- Microcephaly\n- Long philtrum\n- Low-set ears\n- Bulbous nose\n- Wide nose\n- Downslanted palpebral fissures\n- Long eyelashes\n- Thick eyebrow\n- Synophrys\n- Pectus excavatum\n- Hirsutism\n- Brachydactyly\n- Intellectual disability, mild\n- Exaggerated cupid's bow\n- Clinodactyly of the 5th finger\n- Elbow hypertrichosis\n- Curly eyelashes\n- Mild global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10722.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KOOLEN-DE VRIES SYNDROME; KDVS"}],"image":"exported_images\/10723.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BOHRING-OPITZ SYNDROME; BOPS"}],"image":"exported_images\/10724.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10725.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10726.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10727.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10728.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SHORT STATURE, ONYCHODYSPLASIA, FACIAL DYSMORPHISM, AND HYPOTRICHOSIS; SOFT"}],"image":"exported_images\/10729.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OTITIS MEDIA, SUSCEPTIBILITY TO; OMS"}],"image":"exported_images\/10730.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CEREBELLOFACIODENTAL SYNDROME; CFDS"}],"image":"exported_images\/10731.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/10732.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/10733.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/10734.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Hypertelorism\n- Low-set ears\n- Agenesis of corpus callosum\n- Bicoronal synostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CRANIOFRONTONASAL SYNDROME; CFNS"}],"image":"exported_images\/10735.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHARGE SYNDROME"}],"image":"exported_images\/10736.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10737.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10738.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAUCH-STEINDL SYNDROME; RAUST"}],"image":"exported_images\/10739.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10740.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10741.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10742.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10743.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10744.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10745.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10746.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10747.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10748.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 23; MRD23"}],"image":"exported_images\/10749.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DESANTO-SHINAWI SYNDROME; DESSH"}],"image":"exported_images\/10750.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10751.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10752.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10753.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10754.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10755.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10756.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY; CCFDN"}],"image":"exported_images\/10757.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"JOHANSON-BLIZZARD SYNDROME; JBS"}],"image":"exported_images\/10758.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/10759.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/10760.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BORJESON-FORSSMAN-LEHMANN SYNDROME; BFLS"}],"image":"exported_images\/10761.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10762.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MOWAT-WILSON SYNDROME; MOWS"}],"image":"exported_images\/10763.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Linear skin defects with multiple congenital anomalies"}],"image":"exported_images\/10764.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10765.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MYHRE SYNDROME; MYHRS"}],"image":"exported_images\/10766.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KAUFMAN OCULOCEREBROFACIAL SYNDROME; KOS"}],"image":"exported_images\/10767.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Coffin-Siris syndrome"}],"image":"exported_images\/10768.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/10769.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAETHRE-CHOTZEN SYNDROME; SCS"}],"image":"exported_images\/10770.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10771.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10772.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GAPO SYNDROME; GAPOS"}],"image":"exported_images\/10773.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANDIBULOFACIAL DYSOSTOSIS, GUION-ALMEIDA TYPE; MFDGA"}],"image":"exported_images\/10774.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLEIDOCRANIAL DYSPLASIA; CCD"}],"image":"exported_images\/10775.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10776.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10777.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10778.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10779.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10780.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10781.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10782.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COHEN SYNDROME; COH1"}],"image":"exported_images\/10783.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Joubert syndrome"}],"image":"exported_images\/10784.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Orofaciodigital syndrome"}],"image":"exported_images\/10785.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Microphthalmia, syndromic"}],"image":"exported_images\/10786.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Triangular face\n- Abnormal anterior chamber morphology\n- Short clavicles\n- Osteopenia\n- Intellectual disability, mild\n- Hypernasal speech\n- Abnormal cerebral morphology\n- Leukoencephalopathy\n- Delayed skeletal maturation\n- Long nose\n- Myopathy\n- 2-5 finger cutaneous syndactyly\n- Dysharmonic delayed bone age\n- Prematurely aged appearance\n- Asymmetry of the breasts\n- Gluten intolerance\n- Abnormal internal carotid artery morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10787.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10788.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cornelia de Lange syndrome"}],"image":"exported_images\/10789.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 2; DEE2"}],"image":"exported_images\/10790.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Everted lower lip vermilion\n- Downslanted palpebral fissures\n- Nystagmus\n- Atypical behavior\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Exaggerated cupid's bow\n- Prominent forehead\n- Overweight\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SOTOS SYNDROME; SOTOS"}],"image":"exported_images\/10791.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Expressive language delay\n- Celiac disease\n- Intellectual disability, borderline\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10792.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypospadias\n- Wide mouth\n- Thin upper lip vermilion\n- Short philtrum\n- Triangular face\n- Abnormality of the nose\n- Low-set ears\n- Expressive language delay\n- Celiac disease\n- Intellectual disability, borderline\n- Low hanging columella\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10793.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10794.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ANGELMAN SYNDROME; AS"}],"image":"exported_images\/10795.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Triangular face\n- Strabismus\n- Deeply set eye\n- Hypermetropia\n- Autism\n- Delayed speech and language development\n- Cafe-au-lait spot\n- Hypotonia\n- Motor delay\n- Hypertonia\n- Iron deficiency anemia\n- Gastroesophageal reflux\n- Chronic diarrhea\n- Asthma\n- Accelerated skeletal maturation\n- Attention deficit hyperactivity disorder\n- Few cafe-au-lait spots\n- Ankyloglossia\n- Impairment in personality functioning\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY, HYPOTONIA, MUSCULOSKELETAL DEFECTS, AND BEHAVIORAL ABNORMALITIES; DEHMBA"}],"image":"exported_images\/10796.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10797.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10798.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10799.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FLOATING-HARBOR SYNDROME; FLHS"}],"image":"exported_images\/10800.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Hypoplastic labia minora\n- Hydronephrosis\n- Microcephaly\n- Hypothyroidism\n- Intellectual disability\n- Global developmental delay\n- Flexion contracture\n- Talipes equinovarus\n- Ventriculomegaly\n- Scoliosis\n- Thoracolumbar kyphosis\n- Aplasia\/Hypoplasia of the patella\n- Aplasia\/Hypoplasia of the corpus callosum\n- Clitoral hypertrophy\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/10801.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplastic labia majora\n- Hypoplastic labia minora\n- Hydronephrosis\n- Microcephaly\n- Hypothyroidism\n- Intellectual disability\n- Global developmental delay\n- Flexion contracture\n- Talipes equinovarus\n- Ventriculomegaly\n- Scoliosis\n- Thoracolumbar kyphosis\n- Aplasia\/Hypoplasia of the patella\n- Aplasia\/Hypoplasia of the corpus callosum\n- Clitoral hypertrophy\n- Feeding difficulties\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GENITOPATELLAR SYNDROME; GTPTS"}],"image":"exported_images\/10802.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Blepharophimosis\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/10803.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Narrow mouth\n- Cleft palate\n- Microcephaly\n- Retrognathia\n- Hypertelorism\n- Broad forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Low-set ears\n- Sensorineural hearing impairment\n- Wide nasal bridge\n- Ptosis\n- Blepharophimosis\n- Short ribs\n- Intellectual disability\n- Global developmental delay\n- Motor delay\n- Absent speech\n- Joint hypermobility\n- Failure to thrive\n- Abnormal rib cage morphology\n- Patent ductus arteriosus\n- Patent foramen ovale\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Tethered cord\n- Highly arched eyebrow\n- Overfolding of the superior helices\n- Depressed nasal bridge\n- Sparse hair\n- High anterior hairline\n- Midface retrusion\n- Oral aversion\n- Thin eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/10804.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/10805.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/10806.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/10807.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OHDO SYNDROME, SBBYS VARIANT; SBBYSS"}],"image":"exported_images\/10808.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Intellectual disability\n- Severe expressive language delay\n- Severe receptive language delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH HEARING LOSS, SEIZURES, AND BRAIN ABNORMALITIES; NEDHSB"}],"image":"exported_images\/10809.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10810.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10811.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10812.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10813.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10814.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10815.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10816.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10817.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PRADER-WILLI SYNDROME; PWS"}],"image":"exported_images\/10818.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Narrow mouth\n- Thin upper lip vermilion\n- Dolichocephaly\n- Long face\n- Hypertelorism\n- Long philtrum\n- Low-set, posteriorly rotated ears\n- Bulbous nose\n- Short neck\n- Megalocornea\n- Upslanted palpebral fissure\n- Hypertrichosis\n- Downturned corners of mouth\n- Short nose\n- obsolete Thin anteverted nares\n- Prominent metopic ridge\n- Tented upper lip vermilion\n- Staring gaze\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10819.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Anteverted nares\n- Upslanted palpebral fissure\n- Autism\n- Anxiety\n- Omphalocele\n- Ventricular septal defect\n- Atrial septal defect\n- Frontal bossing\n- Short nose\n- Hypopigmented macule\n- Panic attack\n- Periauricular skin pits\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/10820.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Hypertelorism\n- Anteverted nares\n- Upslanted palpebral fissure\n- Autism\n- Anxiety\n- Omphalocele\n- Ventricular septal defect\n- Atrial septal defect\n- Frontal bossing\n- Short nose\n- Hypopigmented macule\n- Panic attack\n- Periauricular skin pits\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Teebi hypertelorism syndrome"}],"image":"exported_images\/10821.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Global developmental delay\n- Anal atresia\n- Asymmetry of the ears\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR"}],"image":"exported_images\/10822.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Hypertelorism\n- Low-set, posteriorly rotated ears\n- Downslanted palpebral fissures\n- Curly hair\n- Sparse hair\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10823.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypertelorism\n- Triangular face\n- Broad forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Short neck\n- Pulmonic stenosis\n- Short stature\n- Decreased body weight\n- Dysplastic pulmonary valve\n- Enlarged thorax\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10824.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10825.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Microretrognathia\n- Macrotia\n- Underdeveloped nasal alae\n- Flared nostrils\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Neonatal hypotonia\n- Short columella\n- Postnatal growth retardation\n- Broad hallux\n- Everted upper lip vermilion\n- Vascular skin abnormality\n- Arrhythmia\n- Cardiogenic shock\n- Palpebral thickening\n- Premature skin wrinkling\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10826.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Posteriorly rotated ears\n- Protruding ear\n- Prominent forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10827.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10828.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10829.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Facial hypotonia\n- Broad forehead\n- Abnormal nasal bridge morphology\n- Anteverted nares\n- Epicanthus inversus\n- Delayed speech and language development\n- Prominent fingertip pads\n- Global developmental delay\n- Tremor\n- Joint laxity\n- Sandal gap\n- Frontal bossing\n- Broad-based gait\n- Neonatal respiratory distress\n- Sudden episodic apnea\n- Short nose\n- Depressed nasal bridge\n- Axial hypotonia\n- EEG with occipital sharp waves\n- EEG with temporal sharp waves\n- Caesarian section\n- Prominent calcaneus\n- Neurodevelopmental delay\n- Weak grip\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10830.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10831.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pierre-Robin sequence\n- Hypermetropia\n- Atypical behavior\n- Autism\n- Hypotonia\n- Abnormal facial shape\n- Intellectual disability, moderate\n- Decreased body weight\n- Talipes valgus\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 26; MRD26"}],"image":"exported_images\/10832.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10833.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10834.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10835.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Intellectual disability\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10836.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Recurrent otitis media\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Cataract\n- Proptosis\n- Shallow orbits\n- Widely spaced teeth\n- Pectus carinatum\n- Prominent scalp veins\n- Retinal atrophy\n- Limited elbow extension\n- Oligohydramnios\n- Calcaneovalgus deformity\n- Short distal phalanx of toe\n- Thoracic kyphosis\n- Elbow flexion contracture\n- Limited knee extension\n- Hypoplasia of the odontoid process\n- Severe short stature\n- Decreased body weight\n- Apneic episodes in infancy\n- Knee flexion contracture\n- Limited shoulder movement\n- Abnormality of retinal pigmentation\n- Acetabular dysplasia\n- Short distal phalanx of finger\n- Dermal translucency\n- High myopia\n- Prominent forehead\n- Upbeat nystagmus\n- Midface retrusion\n- Anterior wedging of T12\n- Tympanosclerosis\n- Posterior staphyloma\n- Pseudophakia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/10837.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Recurrent otitis media\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Cataract\n- Proptosis\n- Shallow orbits\n- Widely spaced teeth\n- Pectus carinatum\n- Prominent scalp veins\n- Retinal atrophy\n- Limited elbow extension\n- Oligohydramnios\n- Calcaneovalgus deformity\n- Short distal phalanx of toe\n- Thoracic kyphosis\n- Elbow flexion contracture\n- Limited knee extension\n- Hypoplasia of the odontoid process\n- Severe short stature\n- Decreased body weight\n- Apneic episodes in infancy\n- Knee flexion contracture\n- Limited shoulder movement\n- Abnormality of retinal pigmentation\n- Acetabular dysplasia\n- Short distal phalanx of finger\n- Dermal translucency\n- High myopia\n- Prominent forehead\n- Upbeat nystagmus\n- Midface retrusion\n- Anterior wedging of T12\n- Tympanosclerosis\n- Posterior staphyloma\n- Pseudophakia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/10838.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide anterior fontanel\n- Recurrent otitis media\n- Conductive hearing impairment\n- Prominent nasal bridge\n- Cataract\n- Proptosis\n- Shallow orbits\n- Widely spaced teeth\n- Pectus carinatum\n- Prominent scalp veins\n- Retinal atrophy\n- Limited elbow extension\n- Oligohydramnios\n- Calcaneovalgus deformity\n- Short distal phalanx of toe\n- Thoracic kyphosis\n- Elbow flexion contracture\n- Limited knee extension\n- Hypoplasia of the odontoid process\n- Severe short stature\n- Decreased body weight\n- Apneic episodes in infancy\n- Knee flexion contracture\n- Limited shoulder movement\n- Abnormality of retinal pigmentation\n- Acetabular dysplasia\n- Short distal phalanx of finger\n- Dermal translucency\n- High myopia\n- Prominent forehead\n- Upbeat nystagmus\n- Midface retrusion\n- Anterior wedging of T12\n- Tympanosclerosis\n- Posterior staphyloma\n- Pseudophakia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"SAUL-WILSON SYNDROME; SWILS"}],"image":"exported_images\/10839.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Duplicated collecting system\n- Macrocephaly\n- Dolichocephaly\n- Long eyelashes\n- Pectus excavatum\n- Hyperpigmentation of the skin\n- Dry skin\n- Hemangioma\n- Hypotonia\n- Global developmental delay\n- Cerebellar vermis hypoplasia\n- Joint laxity\n- Abnormal mitral valve morphology\n- Patent ductus arteriosus\n- Slow-growing hair\n- Short stature\n- Decreased body weight\n- Attention deficit hyperactivity disorder\n- Palmoplantar cutis laxa\n- Sparse hair\n- Delayed fine motor development\n- Prominent forehead\n- Feeding difficulties\n- Extra-axial cerebrospinal fluid accumulation\n- Nasogastric tube feeding\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome-like disorder with loose anagen hair"}],"image":"exported_images\/10840.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Rubinstein-Taybi syndrome"}],"image":"exported_images\/10841.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Tall stature\n- Macrocephaly\n- Depression\n- obsolete Mood swings\n- Autistic behavior\n- Short attention span\n- Anxiety\n- Delayed speech and language development\n- Acne\n- Specific learning disability\n- Obesity\n- Constipation\n- Pneumonia\n- Polyphagia\n- Obstructive sleep apnea\n- Delayed social development\n- Snoring\n- Delayed ability to walk\n- Submucous cleft of soft and hard palate\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/10842.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Broad nasal tip\n- Anteverted nares\n- Deeply set eye\n- Periorbital fullness\n- Atrial septal defect\n- Delayed CNS myelination\n- Depressed nasal bridge\n- Moderate global developmental delay\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FBXW7"}],"image":"exported_images\/10843.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- High palate\n- Recurrent otitis media\n- Wide nose\n- Delayed speech and language development\n- Alternating esotropia\n- Intellectual disability, mild\n- Motor delay\n- Pes planus\n- Dysdiadochokinesis\n- Intention tremor\n- Clumsiness\n- Abnormal periventricular white matter morphology\n- Scoliosis\n- Depressed nasal bridge\n- Lower limb hypertonia\n- Lateral ventricle dilatation\n- Hyperactive patellar reflex\n- Pes valgus\n- Speech apraxia\n- Ankle clonus\n- Hypotropia\n- Hypertropia\n- Anomic aphasia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"HEART AND BRAIN MALFORMATION SYNDROME; HBMS"}],"image":"exported_images\/10844.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Triangular mouth\n- Epicanthus\n- Triangular nasal tip\n- Anteverted nares\n- Strabismus\n- Glandular hypospadias\n- Cyanosis\n- Neonatal hypotonia\n- Atrial septal defect\n- Sudden episodic apnea\n- Short nose\n- Depressed nasal bridge\n- Feeding difficulties in infancy\n- Abnormality of the male genitalia\n- HbH hemoglobin\n- Cardiac conduction abnormality\n- Abnormal ear morphology\n- Abnormal preputium morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"ALPHA-THALASSEMIA\/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"}],"image":"exported_images\/10845.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcephaly\n- Bird-like facies\n- Low-set ears\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Severe short stature\n- Finger clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/10846.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrocephaly\n- Hypertelorism\n- Hearing impairment\n- Webbed neck\n- Short neck\n- Downslanted palpebral fissures\n- Visual impairment\n- Ptosis\n- Abnormality of skin pigmentation\n- Numerous nevi\n- Global developmental delay\n- Atrial septal defect\n- Pulmonic stenosis\n- Curly hair\n- Abnormal EKG\n- Short stature\n- Feeding difficulties in infancy\n- Abnormal ear morphology\n- Left axis deviation\n- Sparse eyebrow\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cardiofaciocutaneous syndrome"}],"image":"exported_images\/10847.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Microcephaly\n- Bird-like facies\n- Sloping forehead\n- Micrognathia\n- Low-set ears\n- Convex nasal ridge\n- Downslanted palpebral fissures\n- Proptosis\n- Global developmental delay\n- Syncope\n- Small for gestational age\n- Sinus bradycardia\n- Proportionate short stature\n- Decreased body weight\n- P wave inversion\n- Deep S wave in lead V5\n- Left axis deviation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Seckel syndrome"}],"image":"exported_images\/10848.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL DELAY WITH OR WITHOUT INTELLECTUAL IMPAIRMENT OR BEHAVIORAL ABNORMALITIES; DDIB"}],"image":"exported_images\/10849.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Broad face\n- Epicanthus\n- Long philtrum\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Visual impairment\n- Blepharophimosis\n- Synophrys\n- Hypotonia\n- Pes planus\n- Gastroesophageal reflux\n- Difficulty walking\n- Short stature\n- Decreased body weight\n- Pes valgus\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Flat face\n- Abnormal ear morphology\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/10850.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Hypospadias\n- Thin upper lip vermilion\n- Microcephaly\n- Broad face\n- Epicanthus\n- Long philtrum\n- Underdeveloped nasal alae\n- Wide nasal bridge\n- Visual impairment\n- Blepharophimosis\n- Synophrys\n- Hypotonia\n- Pes planus\n- Gastroesophageal reflux\n- Difficulty walking\n- Short stature\n- Decreased body weight\n- Pes valgus\n- Bilateral cryptorchidism\n- Tented upper lip vermilion\n- Severe global developmental delay\n- Flat face\n- Abnormal ear morphology\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS"}],"image":"exported_images\/10851.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Prominent antihelix\n- Carious teeth\n- Dental crowding\n- Abnormal dental enamel morphology\n- Autistic behavior\n- Anxiety\n- Delayed speech and language development\n- Intellectual disability, mild\n- Global developmental delay\n- Exaggerated cupid's bow\n- Febrile seizure (within the age range of 3 months to 6 years)\n- High, narrow palate\n- Clinodactyly of the 5th finger\n- Preauricular pit\n- Prominent crus of helix\n- Supernumerary tooth\n- Chronic constipation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Autism, susceptiblity to"}],"image":"exported_images\/10852.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Facial hypotonia\n- Optic atrophy\n- Abnormality of visual evoked potentials\n- Global developmental delay\n- Absent speech\n- Plagiocephaly\n- Laryngomalacia\n- Cerebral atrophy\n- Hypoplasia of the corpus callosum\n- Focal clonic seizure\n- Hypsarrhythmia\n- Severe muscular hypotonia\n- Bilateral cryptorchidism\n- Epileptic spasm\n- Myoclonic seizure\n- Optic nerve gray crescent\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 28; DEE28"}],"image":"exported_images\/10853.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Cataract\n- Aggressive behavior\n- Hypertension\n- Intellectual disability, moderate\n- Focal-onset seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CDH8"}],"image":"exported_images\/10854.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macrocephaly\n- Autistic behavior\n- Large for gestational age\n- 2-3 toe syndactyly\n- Vascular skin abnormality\n- Mild global developmental delay\n- Abnormal cerebral venous sinus morphology\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME; MCAP"}],"image":"exported_images\/10855.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Proptosis\n- Increased intracranial pressure\n- Obstructive sleep apnea\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10856.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypoplasia of the maxilla\n- Proptosis\n- Dental malocclusion\n- Papilledema\n- Visual field defect\n- Increased intracranial pressure\n- Obstructive sleep apnea\n- Bicoronal synostosis\n- Abnormal stereopsis\n- Lagophthalmos\n- Ocular pain\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10857.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Conductive hearing impairment\n- Choanal stenosis\n- Proptosis\n- Brachydactyly\n- Motor delay\n- Increased intracranial pressure\n- Abnormality of the skull base\n- Upper airway obstruction\n- Obstructive sleep apnea\n- Respiratory failure\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Prolonged neonatal jaundice\n- Broad hallux\n- Abnormality of the nasal cavity\n- Abnormal hair whorl\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Respiratory tract infection\n- Snoring\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/10858.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Brachycephaly\n- Conductive hearing impairment\n- Choanal stenosis\n- Proptosis\n- Brachydactyly\n- Motor delay\n- Increased intracranial pressure\n- Abnormality of the skull base\n- Upper airway obstruction\n- Obstructive sleep apnea\n- Respiratory failure\n- Sagittal craniosynostosis\n- Lambdoidal craniosynostosis\n- Depressed nasal bridge\n- Prominent metopic ridge\n- Prolonged neonatal jaundice\n- Broad hallux\n- Abnormality of the nasal cavity\n- Abnormal hair whorl\n- Broad thumb\n- Bicoronal synostosis\n- Midface retrusion\n- Respiratory tract infection\n- Snoring\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PFEIFFER SYNDROME"}],"image":"exported_images\/10859.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- Broad forehead\n- Micrognathia\n- Small forehead\n- Small earlobe\n- Thickened helices\n- Bulbous nose\n- Overfolding of the superior helices\n- Attached earlobe\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/10860.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long face\n- Large forehead\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10861.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Short philtrum\n- Widely-spaced maxillary central incisors\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10862.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: European\n\nObserved phenotypic features:\n- Pointed chin\n- Short philtrum\n- Short chin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10863.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10864.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10865.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10866.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10867.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10868.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10869.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide mouth\n- Open mouth\n- High palate\n- Microcephaly\n- Long face\n- Coarse facial features\n- Mandibular prognathia\n- Hypomimic face\n- Macrotia\n- Prominent nasal bridge\n- Strabismus\n- Aggressive behavior\n- Autistic behavior\n- Delayed speech and language development\n- Hyperactivity\n- Delayed puberty\n- Seizure\n- Global developmental delay\n- Growth delay\n- Hallux valgus\n- Constipation\n- Poor suck\n- Broad-based gait\n- Clumsiness\n- Sleep disturbance\n- Long nose\n- Clinodactyly of the 5th finger\n- Almond-shaped palpebral fissure\n- Low hanging columella\n- Cone-shaped epiphyses of the phalanges of the hand\n- Intellectual disability, severe\n- Arm dystonia\n- Narrow palpebral fissure\n- Crouch gait\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10870.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Microcephaly\n- Low-set ears\n- Wide nasal bridge\n- Aggressive behavior\n- Short attention span\n- Delayed speech and language development\n- Hirsutism\n- Hypotonia\n- Oligohydramnios\n- Unsteady gait\n- Intellectual disability, moderate\n- Sleep disturbance\n- Febrile seizure (within the age range of 3 months to 6 years)\n- Long nose\n- Short stature\n- Microtia\n- Obsessive-compulsive trait\n- Exodeviation\n- Frequent temper tantrums\n- Recurrent ear infections\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10871.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Wide nasal bridge\n- Strabismus\n- Downslanted palpebral fissures\n- Ptosis\n- Autistic behavior\n- Delayed speech and language development\n- Hypotonia\n- Joint laxity\n- Decreased fetal movement\n- Polyhydramnios\n- Pes planus\n- Constipation\n- Myopathic facies\n- Gait ataxia\n- Generalized non-motor (absence) seizure\n- Intellectual disability, moderate\n- Sleep disturbance\n- Hyperlordosis\n- Capillary hemangioma\n- Poor fine motor coordination\n- Echolalia\n- Atonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 5; MRD5"}],"image":"exported_images\/10872.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Abnormal repetitive mannerisms\n- Global developmental delay\n- Absent speech\n- Bilateral tonic-clonic seizure\n- Inability to walk\n- Focal hemiclonic seizure\n- Epileptic spasm\n- Neck muscle hypertrophy\n- Myoclonic seizure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 4; DEE4"}],"image":"exported_images\/10873.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Glossoptosis\n- Wide anterior fontanel\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Proptosis\n- Myopia\n- Optic atrophy\n- Synophrys\n- Abnormality of the vertebral column\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Tracheomalacia\n- Short nose\n- Short stature\n- Cervical C2\/C3 vertebral fusion\n- Aspiration pneumonia\n- Bronchitis\n- Unilateral cryptorchidism\n- Hip subluxation\n- Sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/10874.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Glossoptosis\n- Wide anterior fontanel\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Proptosis\n- Myopia\n- Optic atrophy\n- Synophrys\n- Abnormality of the vertebral column\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Tracheomalacia\n- Short nose\n- Short stature\n- Cervical C2\/C3 vertebral fusion\n- Aspiration pneumonia\n- Bronchitis\n- Unilateral cryptorchidism\n- Hip subluxation\n- Sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/10875.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Vesicoureteral reflux\n- Glossoptosis\n- Wide anterior fontanel\n- Long philtrum\n- Micrognathia\n- Hearing impairment\n- Anteverted nares\n- Proptosis\n- Myopia\n- Optic atrophy\n- Synophrys\n- Abnormality of the vertebral column\n- Brachydactyly\n- Intellectual disability\n- Global developmental delay\n- Obesity\n- Small for gestational age\n- Laryngomalacia\n- Ventricular septal defect\n- Patent ductus arteriosus\n- Delayed skeletal maturation\n- Tracheal stenosis\n- Tracheomalacia\n- Short nose\n- Short stature\n- Cervical C2\/C3 vertebral fusion\n- Aspiration pneumonia\n- Bronchitis\n- Unilateral cryptorchidism\n- Hip subluxation\n- Sepsis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHOPS SYNDROME; CHOPS"}],"image":"exported_images\/10876.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DEAFNESS, CATARACT, IMPAIRED INTELLECTUAL DEVELOPMENT, AND POLYNEUROPATHY; DCIDP"}],"image":"exported_images\/10877.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10878.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10879.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Synophrys\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10880.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- High forehead\n- Low-set, posteriorly rotated ears\n- Webbed neck\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10881.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- High forehead\n- Low-set, posteriorly rotated ears\n- Thickened helices\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10882.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- Thick lower lip vermilion\n- Hypertelorism\n- Triangular face\n- Downslanted palpebral fissures\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10883.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Long eyelashes\n- Highly arched eyebrow\n- Sparse lateral eyebrow\n- Eversion of lateral third of lower eyelids\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Kabuki syndrome"}],"image":"exported_images\/10884.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Epicanthus\n- Bulbous nose\n- Prominent nasal bridge\n- Wide nasal bridge\n- Telecanthus\n- Ptosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/10885.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n- Prominent nasal bridge\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/10886.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Bulbous nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL"}],"image":"exported_images\/10887.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Hypertelorism\n- Broad forehead\n- Micrognathia\n- Low-set, posteriorly rotated ears\n- Webbed neck\n- Downslanted palpebral fissures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10888.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Glaucoma\n- Cataract\n- Hashimoto thyroiditis\n- Lymphedema\n- Abnormal mitral valve morphology\n- Pulmonic stenosis\n- Chylothorax\n- Neuroendocrine neoplasm\n- Gastrointestinal stroma tumor\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Noonan syndrome"}],"image":"exported_images\/10889.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Neurogenic bladder\n- Cryptorchidism\n- Vesicoureteral reflux\n- Hydronephrosis\n- Open mouth\n- High palate\n- Turricephaly\n- Long face\n- Thickened helices\n- Megalocornea\n- Ptosis\n- Hypermetropia\n- Long palpebral fissure\n- Delayed speech and language development\n- Pectus excavatum\n- Sacral dimple\n- Hypohidrosis\n- Skin rash\n- Hypotonia\n- Intellectual disability, mild\n- Hyporeflexia\n- Hip dysplasia\n- Bicuspid aortic valve\n- Overlapping toe\n- Vomiting\n- Diarrhea\n- Constipation\n- Gastroesophageal reflux\n- Migraine\n- Intellectual disability, moderate\n- Supernumerary nipple\n- Gastroparesis\n- Scoliosis\n- Exaggerated median tongue furrow\n- Downturned corners of mouth\n- Inverted nipples\n- Cleft ala nasi\n- Vertebral segmentation defect\n- CNS hypomyelination\n- Intestinal pseudo-obstruction\n- Aortic aneurysm\n- Sparse lateral eyebrow\n- Prominent metopic ridge\n- Agenesis of incisor\n- Attention deficit hyperactivity disorder\n- Impaired pain sensation\n- Hypoplastic helices\n- Bifid tongue\n- Polydactyly\n- Agenesis of molar\n- Wide nasal ridge\n- Lagophthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"AU-KLINE SYNDROME; AUKS"}],"image":"exported_images\/10890.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WIEDEMANN-STEINER SYNDROME; WDSTS"}],"image":"exported_images\/10891.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/10892.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 6, WITH OR WITHOUT SEIZURES; MRD6"}],"image":"exported_images\/10893.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, AUTOSOMAL DOMINANT; NDHMSD"}],"image":"exported_images\/10894.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Three M syndrome"}],"image":"exported_images\/10895.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Delayed speech and language development\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH SEVERE MOTOR IMPAIRMENT AND ABSENT LANGUAGE; NEDMIAL"}],"image":"exported_images\/10896.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Macroglossia\n- Open mouth\n- Coarse facial features\n- Hearing impairment\n- Short neck\n- Synophrys\n- Widely spaced teeth\n- Seizure\n- Ataxia\n- Global developmental delay\n- Cerebellar atrophy\n- Hyperreflexia\n- Hammertoe\n- Talipes equinovalgus\n- Babinski sign\n- Periventricular white matter hyperintensities\n- Thin corpus callosum\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/10897.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Brachycephaly\n- Coarse facial features\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"MANNOSIDOSIS, ALPHA B, LYSOSOMAL; MANSA"}],"image":"exported_images\/10898.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Coarse facial features\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Mucopolysaccharidoses"}],"image":"exported_images\/10899.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Wide mouth\n- Coarse facial features\n- Long philtrum\n- Wide nasal bridge\n- Anteverted nares\n- Strabismus\n- Long eyelashes\n- Thick eyebrow\n- Broad palm\n- Global developmental delay\n- Atrial septal defect\n- Elevated circulating alkaline phosphatase concentration\n- Prominent forehead\n- Thick vermilion border\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyperphosphatasia with mental retardation syndrome"}],"image":"exported_images\/10900.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OGDEN SYNDROME; OGDNS"}],"image":"exported_images\/10901.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormal palate morphology\n- Large fontanelles\n- Low anterior hairline\n- Mandibular prognathia\n- Round face\n- Hypertelorism\n- Broad nasal tip\n- Thick eyebrow\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Reduced eye contact\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Absent speech\n- Pes planus\n- Short toe\n- Bilateral tonic-clonic seizure\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Mutism\n- Developmental regression\n- Focal impaired awareness seizure\n- Clinodactyly of the 5th finger\n- Short stature\n- Relative macrocephaly\n- Bilateral single transverse palmar creases\n- Atonic seizure\n- Focal emotional seizure with laughing\n- Prominent forehead\n- Abnormal social behavior\n- Thick vermilion border\n- Neurodevelopmental delay\n- Tonic seizure\n- Myoclonic seizure\n- Motor regression\n- Reduced blood 5-methyltetrahydrofolate level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10902.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormal palate morphology\n- Large fontanelles\n- Low anterior hairline\n- Mandibular prognathia\n- Round face\n- Hypertelorism\n- Broad nasal tip\n- Thick eyebrow\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Reduced eye contact\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Absent speech\n- Pes planus\n- Short toe\n- Bilateral tonic-clonic seizure\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Mutism\n- Developmental regression\n- Focal impaired awareness seizure\n- Clinodactyly of the 5th finger\n- Short stature\n- Relative macrocephaly\n- Bilateral single transverse palmar creases\n- Atonic seizure\n- Focal emotional seizure with laughing\n- Prominent forehead\n- Abnormal social behavior\n- Thick vermilion border\n- Neurodevelopmental delay\n- Tonic seizure\n- Myoclonic seizure\n- Motor regression\n- Reduced blood 5-methyltetrahydrofolate level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10903.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cryptorchidism\n- Abnormal palate morphology\n- Large fontanelles\n- Low anterior hairline\n- Mandibular prognathia\n- Round face\n- Hypertelorism\n- Broad nasal tip\n- Thick eyebrow\n- Macrodontia of permanent maxillary central incisor\n- Autistic behavior\n- Reduced eye contact\n- Brachydactyly\n- Intellectual disability\n- Seizure\n- Absent speech\n- Pes planus\n- Short toe\n- Bilateral tonic-clonic seizure\n- Ventriculomegaly\n- Exaggerated cupid's bow\n- Mutism\n- Developmental regression\n- Focal impaired awareness seizure\n- Clinodactyly of the 5th finger\n- Short stature\n- Relative macrocephaly\n- Bilateral single transverse palmar creases\n- Atonic seizure\n- Focal emotional seizure with laughing\n- Prominent forehead\n- Abnormal social behavior\n- Thick vermilion border\n- Neurodevelopmental delay\n- Tonic seizure\n- Myoclonic seizure\n- Motor regression\n- Reduced blood 5-methyltetrahydrofolate level\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KBG SYNDROME; KBGS"}],"image":"exported_images\/10904.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Flexion contracture\n- Failure to thrive\n- Dysphagia\n- Short stature\n- Decreased body weight\n- Ankylosis of feet small joints\n- Patellar subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10905.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Flexion contracture\n- Failure to thrive\n- Dysphagia\n- Short stature\n- Decreased body weight\n- Ankylosis of feet small joints\n- Patellar subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10906.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Flexion contracture\n- Failure to thrive\n- Dysphagia\n- Short stature\n- Decreased body weight\n- Ankylosis of feet small joints\n- Patellar subluxation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10907.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Narrow mouth\n- High palate\n- Everted lower lip vermilion\n- Hypertelorism\n- Long philtrum\n- Whistling appearance\n- Micrognathia\n- Wide nasal bridge\n- Strabismus\n- Deeply set eye\n- Blepharophimosis\n- Slender finger\n- Bilateral talipes equinovarus\n- Short nose\n- Everted upper lip vermilion\n- Chin with H-shaped crease\n- Long fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10908.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Clitoral hypoplasia\n- Abnormality of the dentition\n- Triangular mouth\n- Gingival overgrowth\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- High forehead\n- Hearing impairment\n- Anteverted nares\n- Hypermetropia\n- Impaired social interactions\n- Brachydactyly\n- Intellectual disability, mild\n- Global developmental delay\n- Frontal bossing\n- Nail dysplasia\n- Scoliosis\n- Obstructive sleep apnea\n- Mesomelia\n- Short nose\n- Broad hallux\n- Hypoplasia of the anterior nasal spine\n- Increased bone mineral density\n- Broad thumb\n- Midface retrusion\n- Abnormal labia minora morphology\n- Clinodactyly\n- Increased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/10909.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Clitoral hypoplasia\n- Abnormality of the dentition\n- Triangular mouth\n- Gingival overgrowth\n- Thin upper lip vermilion\n- Macrocephaly\n- Epicanthus\n- Hypertelorism\n- Long philtrum\n- Micrognathia\n- High forehead\n- Hearing impairment\n- Anteverted nares\n- Hypermetropia\n- Impaired social interactions\n- Brachydactyly\n- Intellectual disability, mild\n- Global developmental delay\n- Frontal bossing\n- Nail dysplasia\n- Scoliosis\n- Obstructive sleep apnea\n- Mesomelia\n- Short nose\n- Broad hallux\n- Hypoplasia of the anterior nasal spine\n- Increased bone mineral density\n- Broad thumb\n- Midface retrusion\n- Abnormal labia minora morphology\n- Clinodactyly\n- Increased head circumference\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Robinow syndrome"}],"image":"exported_images\/10910.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Cleft palate\n- Pierre-Robin sequence\n- Whistling appearance\n- Micrognathia\n- Seizure\n- Hypotonia\n- Polyhydramnios\n- Distal arthrogryposis\n- Postnatal growth retardation\n- Severe global developmental delay\n- Neonatal asphyxia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Arthrogryposis, distal"}],"image":"exported_images\/10911.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n- Hypoplasia of the maxilla\n- Congenital diaphragmatic hernia\n- Osteoporosis\n- Cutis laxa\n- Joint laxity\n- Abnormal facial shape\n- Wormian bones\n- Dermatochalasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"GERODERMA OSTEODYSPLASTICUM; GO"}],"image":"exported_images\/10912.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Macrotia\n- Osteopenia\n- Cutis laxa\n- Adducted thumb\n- Joint laxity\n- Intrauterine growth retardation\n- Short nose\n- Central nervous system degeneration\n- Hernia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/10913.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Cutis laxa\n- Intrauterine growth retardation\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/10914.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Triangular face\n- Long philtrum\n- Osteopenia\n- Cutis laxa\n- Joint laxity\n- Intrauterine growth retardation\n- Wormian bones\n- Hip dislocation\n- Short nose\n- Central nervous system degeneration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/10915.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/10916.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Oculocutaneous albinism"}],"image":"exported_images\/10917.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Small scrotum\n- Hearing impairment\n- Small earlobe\n- Deeply set eye\n- Delayed speech and language development\n- Intellectual disability\n- Seizure\n- Global developmental delay\n- Motor delay\n- Gait disturbance\n- Generalized hypotonia\n- Absent speech\n- Joint laxity\n- Congenital thrombocytopenia\n- Abnormal facial shape\n- Gait imbalance\n- Delayed gross motor development\n- Unsteady gait\n- Intellectual disability, moderate\n- Scoliosis\n- Thoracolumbar scoliosis\n- CNS hypomyelination\n- Bone marrow hypocellularity\n- Poor fine motor coordination\n- Microtia\n- Delayed fine motor development\n- Gastrostomy tube feeding in infancy\n- Feeding difficulties\n- Abnormality of brain morphology\n- Retractile testis\n- Neurodevelopmental delay\n- Cognitive impairment\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PSMC5"}],"image":"exported_images\/10918.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Waardenburg syndrome"}],"image":"exported_images\/10919.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/10920.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Long philtrum\n- Posteriorly rotated ears\n- Wide nose\n- Downslanted palpebral fissures\n- Short nose\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Cutis laxa"}],"image":"exported_images\/10921.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Long face\n- Round face\n- Smooth philtrum\n- Hypoplasia of the maxilla\n- Broad forehead\n- Long philtrum\n- Low-set ears\n- Webbed neck\n- Short neck\n- Brachydactyly\n- Joint dislocation\n- Joint hypermobility\n- Abnormality of the cardiovascular system\n- Congestive heart failure\n- Cardiomyopathy\n- Pes planus\n- Scoliosis\n- Short stature\n- Decreased body weight\n- Broad thumb\n- Chronic pain\n- Abnormal oral morphology\n- Long thumb\n- Abnormality of the musculoskeletal system\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2"}],"image":"exported_images\/10922.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: African\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"COGNITIVE FUNCTION 1, SOCIAL; CGF1"}],"image":"exported_images\/10923.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/10924.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA; NEDDISH"}],"image":"exported_images\/10925.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/10926.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/10927.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"RAHMAN SYNDROME; RMNS"}],"image":"exported_images\/10928.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3A"}],"image":"exported_images\/10929.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H3-3B"}],"image":"exported_images\/10930.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/10931.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Blue sclerae\n- Dentinogenesis imperfecta\n- Recurrent fractures\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Osteogenesis imperfecta"}],"image":"exported_images\/10932.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: African\n\nObserved phenotypic features:\n- Neurofibromas\n- Multiple cafe-au-lait spots\n- Plexiform neurofibroma\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"NEUROFIBROMATOSIS, TYPE I; NF1"}],"image":"exported_images\/10933.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Upslanted palpebral fissure\n- Global developmental delay\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DOWN SYNDROME"}],"image":"exported_images\/10934.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"H4C5"}],"image":"exported_images\/10935.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TCEAL1"}],"image":"exported_images\/10936.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LESSEL-KREIENKAMP SYNDROME; LESKRES"}],"image":"exported_images\/10937.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECK-FAHRNER SYNDROME; BEFAHRS"}],"image":"exported_images\/10938.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Exotropia\n- Photophobia\n- Bruising susceptibility\n- Hypopigmentation of the skin\n- Ocular albinism\n- Abnormality of thrombocytes\n- Prolonged bleeding time\n- Impaired platelet aggregation\n- Horizontal jerk nystagmus\n- Reduced visual acuity\n- Hypoplasia of the fovea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/10939.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Exotropia\n- Photophobia\n- Bruising susceptibility\n- Hypopigmentation of the skin\n- Ocular albinism\n- Abnormality of thrombocytes\n- Prolonged bleeding time\n- Impaired platelet aggregation\n- Horizontal jerk nystagmus\n- Reduced visual acuity\n- Hypoplasia of the fovea\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hermansky-Pudlak syndrome"}],"image":"exported_images\/10940.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: African\n\nObserved phenotypic features:\n- Intrauterine growth retardation\n- Small for gestational age\n- Toe syndactyly\n- Thrombocytopenia\n- Lymphopenia\n- Anemia\n- Bone marrow hypocellularity\n- Severe global developmental delay\n- Wheezing\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"LIG4 SYNDROME"}],"image":"exported_images\/10941.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10942.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Mandibular prognathia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10943.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Mandibular prognathia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10944.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"TMEM147"}],"image":"exported_images\/10945.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Alagille syndrome"}],"image":"exported_images\/10946.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/10947.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Eczema\n- Eosinophilia\n- Leukocytosis\n- Increased circulating IgE level\n- Elevated erythrocyte sedimentation rate\n- Recurrent bacterial skin infections\n- Elevated circulating C-reactive protein concentration\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/10948.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Eczema\n- Asthma\n- Increased circulating IgE level\n- Recurrent bacterial skin infections\n- Decreased specific pneumococcal antibody level\n- Food allergy\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hyper-IgE recurrent infection syndrome"}],"image":"exported_images\/10949.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Long philtrum\n- Low-set ears\n- Anteverted nares\n- Astigmatism\n- Deeply set eye\n- Delayed speech and language development\n- Hypotonia\n- Global developmental delay\n- Motor delay\n- Joint hypermobility\n- Short nose\n- Depressed nasal bridge\n- Large earlobe\n- Low hanging columella\n- Narrow palpebral fissure\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CLARK-BARAITSER SYNDROME; CLABARS"}],"image":"exported_images\/10950.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Wide nasal bridge\n- Atopic dermatitis\n- Mutism\n- Scoliosis\n- Recurrent infections\n- Recurrent upper respiratory tract infections\n- Decreased circulating total IgM\n- Depressed nasal bridge\n- Abnormal tracheobronchial morphology\n- Infection following live vaccination\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Immunodeficiency-centromeric instability-facial anomalies"}],"image":"exported_images\/10951.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Others\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"VICI SYNDROME; VICIS"}],"image":"exported_images\/10952.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Abnormality of the face\n- Failure to thrive\n- Diarrhea\n- Woolly hair\n- Brittle hair\n- Multiple cafe-au-lait spots\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichohepatoenteric syndrome"}],"image":"exported_images\/10953.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Epicanthus\n- Hypertelorism\n- Thick eyebrow\n- Lymphedema\n- Depressed nasal bridge\n- Abnormal hair whorl\n- Lymphangiectasis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Hennekam lymphangiectasia-lymphedema syndrome"}],"image":"exported_images\/10954.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Macrotia\n- Thick eyebrow\n- Autism\n- Hypertrichosis\n- 2-3 finger syndactyly\n- Intellectual disability\n- Hypotonia\n- Global developmental delay\n- Almond-shaped palpebral fissure\n- Cleft lip\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CHUNG-JANSEN SYNDROME; CHUJANS"}],"image":"exported_images\/10955.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"OPITZ-KAVEGGIA SYNDROME; OKS"}],"image":"exported_images\/10956.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- Cryptorchidism\n- Hydrocephalus\n- Carious teeth\n- Dry skin\n- Seizure\n- Hepatosplenomegaly\n- Onychogryposis\n- Thrombocytopenia\n- Neutropenia\n- Anemia\n- Neonatal hypoglycemia\n- Increased serum lactate\n- Recurrent infections\n- Abnormality of bone mineral density\n- Spotty hypopigmentation\n- Lung abscess\n- Scaling skin\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"POIKILODERMA WITH NEUTROPENIA; PN"}],"image":"exported_images\/10957.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Microcornea\n- Aniridia\n- Chorioretinal coloboma\n- Ectropion\n- Horizontal nystagmus\n- Lens subluxation\n- Orbital cyst\n- Bilateral microphthalmos\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"DIGEORGE SYNDROME; DGS"}],"image":"exported_images\/10958.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Holoprosencephaly"}],"image":"exported_images\/10959.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/10960.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/10961.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/10962.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/10963.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WEISS-KRUSZKA SYNDROME; WSKA"}],"image":"exported_images\/10964.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10965.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10966.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10967.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hypotonia\n- Motor delay\n- Increased serum lactate\n- Leukodystrophy\n- Increased serum pyruvate\n- Decreased body weight\n- Postnatal growth retardation\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"WOLF-HIRSCHHORN SYNDROME; WHS"}],"image":"exported_images\/10968.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: European\n\nObserved phenotypic features:\n- Attention deficit hyperactivity disorder\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"KDM2B"}],"image":"exported_images\/10969.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Macroglossia\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"BECKWITH-WIEDEMANN SYNDROME; BWS"}],"image":"exported_images\/10970.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN"}],"image":"exported_images\/10971.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Hyperopic astigmatism\n- Autistic behavior\n- Hypotonia\n- Intellectual disability, mild\n- Global developmental delay\n- Absent speech\n- Sleep disturbance\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"PHELAN-MCDERMID SYNDROME; PHMDS"}],"image":"exported_images\/10972.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Developmental cataract\n- Papilledema\n- Scoliosis\n- Obstructive sleep apnea\n- Coronal craniosynostosis\n- Broad hallux\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10973.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: unknown\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Developmental cataract\n- Papilledema\n- Scoliosis\n- Obstructive sleep apnea\n- Coronal craniosynostosis\n- Broad hallux\n- Midface retrusion\n- Clinodactyly\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10974.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Thin vermilion border\n- Broad forehead\n- Long philtrum\n- Micrognathia\n- Low-set ears\n- Pear-shaped nose\n- Dental malocclusion\n- Brachydactyly\n- Fine hair\n- Slow-growing hair\n- Sparse lateral eyebrow\n- Nail dystrophy\n- Prominent ear helix\n- Cone-shaped epiphysis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10975.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: female\n- Ethnicity: European\n\nObserved phenotypic features:\n- Thin upper lip vermilion\n- Long philtrum\n- Micrognathia\n- Pear-shaped nose\n- Short neck\n- Broad neck\n- obsolete Sparse and thin eyebrow\n- Brachydactyly\n- Joint hypermobility\n- Fragile nails\n- Recurrent respiratory infections\n- Slow-growing hair\n- Fair hair\n- Sparse lateral eyebrow\n- Sparse hair\n- Cone-shaped epiphysis\n- Shortening of all phalanges of fingers\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"Trichorhinophalangeal syndrome"}],"image":"exported_images\/10976.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10977.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Asian\n\nObserved phenotypic features:\n- None reported\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"FRAGILE X SYNDROME; FXS"}],"image":"exported_images\/10978.png"} +{"conversations":[{"from":"human","value":"\nYou are a clinical decision support system for rare genetic syndromes.\n\nPatient information:\n- Sex: male\n- Ethnicity: Unknown\n\nObserved phenotypic features:\n- Lens subluxation\n- Craniosynostosis\n\nQuestion:\nWhat is the most likely diagnosis?"},{"from":"gpt","value":"CROUZON SYNDROME"}],"image":"exported_images\/10979.png"}