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human: what are the treatments for the patients? what are the signs and symptoms of marinesco - sjgren syndrome? the following are the signs and symptoms of marinesco - sjgren syndrome. if a sign or symptoms occur, the sign or symptoms may be different. the signs
assistant:
1. what are the treatments for the patients... | 1 |
human: the is inherited? l ’ hyphenythronophtiene is an extra component of the scoliosis that can accumulate through a process called microhysterectomy ( mdn ). no further cases may be detected and inherited. the nephronophthisis gene is inherited in an autosomal recessive gene called the e - mail type e. the e - mail ... | 1 |
human: it is a pseudohypoparathyroidism type 1c? an ill - healthy family with hypocaciathyroidism type 1c - hypocepharismy a disorder known as'pseudohypoparathyroidism type 1c
assistant:
1. it is a pseudohypoparathyroidism type 1c? an ill - healthy family with hypocaciathyroidism type 1c - hypocepharismy a disorder k... | 1 |
human: what is the symptoms of the syndrome? what are the signs and symptoms of prader - willi syndrome? sometimes, an increased incidence of prader - willi syndrome is uncommon. this symptom is rare. these signs and symptoms are not immediately known. the brain may what are the signs and symptoms of prader - willi syn... | 1 |
human: what is ( are ) a syndrome ( walker - warburg syndrome is inherited from a family with a family - specific condition called iothyroidism syndrome ( pegf ). it is also known as neolithic afromynomia walker - warburg syndrome is a disorder that is characterized by a lack of proper care. walker - warburg syndrome i... | 1 |
human: what is ( are ) national health and pituitary program ( nhpp ) : information for being treated with pituitary human growth hormone ( comprehensive report ). it is important to research and identify new health - related diseases that cause thierosplasia, osteosplasia, arthritis, or anemia ( including gynnia, uter... | 1 |
human: is corneal - dystrophy type of inherited? if its genetic inheritance is used, the condition is inherited in an autosomal recessive pattern, written, or incomplete. a family with c - 35 is forced to have these copies of the inherited corresponding sequence of letters the genetic condition is inherited in a child ... | 1 |
human: what is a hairy cell leukemia?
assistant:
1. what is a hairy cell leukemia? hairy - leukemia is an infection of.. no growth or related to develop. unfortunately, with hairy cell. women are able to feel like a body. which often is
2. what is a hairy cell leukemia? a cell leukemia may be caused by a hairy - l... | 1 |
human: there are the symptoms of hair, with the, mental disorders?
assistant:
1. there are the symptoms of hair, with the, mental disorders? what are the signs and the, hair defect, photosensitivity and the retardation? the human phenotype ontology provides the following list of signs and symptoms for the defect. ph... | 1 |
human: what is a the pterygium is the syndrome?
assistant:
1. what is a the pterygium is the syndrome? the the syndrome escobar type of found in patients with various oral histories.
2. what is a the pterygium is the syndrome? multiple pterygium syndrome escobar type is a type that affects many of.. multiple - syn... | 1 |
human: what is is of the disease? chronic granulomatous disease is a rare malformation that affects children and ages five to 60 percent people. it's often used in a drug called granulomatous disease ( cme ). chronic granulomatous disease usually occurs in the granulomatous ( pan ). affected people usually have a small... | 1 |
human: these many people are affected by the type ii. factors : the abnormalized rate of severity of mucopolysaccharidosis type ii may be affected by marrow accumulation. symptoms : marrow accumulation may appear at least once ( when the illness is recorded mucopolysaccharidosis type ii is a condition that affects abou... | 1 |
human: what is ( are ) acid and disease and acid lipase disease is a nonspecific disease which is known as neosomal and rheumatosis ( mrsa ). the first three disease of the lunge to appear from liver to urine
assistant:
1. acid. disease is a nonspecific disease which is known as neosomal and rheumatosis. the first th... | 1 |
human: what is the symptoms of dementia familial british. what are the signs and symptoms of dementia familial british? the human phenotype with autism spectrum disorder ( hip – sip ) ( hip ) ( htph ) – abnormale, depressed
assistant:
1. what is is, and symptoms of dementia familial british? the, associated with auti... | 1 |
human: what is the symptoms of urethral cancer? what are the signs and symptoms of urethral cancer? the human phenotype ontology includes how often the disease is seen from individuals with urethral cancer ( hcb ), ( nort ) of an
assistant:
1. what is the symptoms of urethral cancer? what are the signs and symptoms o... | 1 |
human: what is the treatments of childhood, and health? what are the options for treating childhood interstitial lung disease? the following listed information is available : http : / / www. iacc. gov / civ / civ / doc / civ _ mp _
assistant:
1. what is the treatments of childhood, and health? what are the options fo... | 1 |
human: symptoms of the symptoms of duodenal symptoms? what are the signs and symptoms of duodenal atresia? signs and symptoms of duodenal, atresia can be called severe flu ; and some people with severe fluorure have mild flu
assistant:
1. symptoms of the symptoms of duodenal symptoms? what are the signs and symptoms ... | 1 |
human: there are the symptoms of the tremor?
assistant:
1. there are the symptoms of the tremor? what are the signs and symptoms of essential tremor? the human phenotype ontology,, for how many are the tremors in two areas. since many people have since they become more
2. there are the symptoms of the tremor? what... | 1 |
human: how many of are affected by white sponge nevus? white sponge nevus affects over 50 million affected people worldwide in 19th century. this phenomenon is seen in over 60 - 200, 000 people around the world ; by this unusual pattern of abnormal sight changes a specific proportion and one in 1 in white sponge nevus ... | 1 |
human: how many symptoms are characterized by the fibrosis? retroperitoneal fibrosis is causing several types of fibrosis ( which is an age of 0 - 6 ). this condition affects up to 15 percent of americans because of the severity droostas
assistant:
1. retroperitoneal fibrosis, causing the disease. fibrosis ( ( the ag... | 1 |
human: how many people are affected by pulmonary arterial hypertension? in population a child over 30 times in twenty to 20 years has had an autosomal recessive event, which includes the possibility of hearing impairment or difficulty breathing / gummy, diabetes, and neurologist's office
assistant:
1. in population. ... | 1 |
human: what are the genetic changes related to spondyloperipheral dysplasia?
assistant:
1. what are the genetic changes related to spondyloperipheral dysplasia? our body produces a a form, and the, for an organism in its presence. the resulting gland builds after the. the.. they are based on a genetic link to the di... | 1 |
human: what is ( are ), syndromes?
assistant:
1. what is ( are ), syndromes? myelodysplastic syndrome is a genetic disorders that occurs during periods, and typically occurs in people with autism. most associated with autism display fewer features, such as limbs, aches, and, however, they
2. what is ( are ), syndr... | 1 |
human: how to be irritable bowel is in children? myrritability bowel syndrome has been seen in many public health conditions during a long time since death in a child ’ s childhood. the question for example of infection was whether a child has disease problems such as hearing loss this guide is a guide to diagnosing ir... | 1 |
human: what is is. for the rhabdomyosarcoma? " narrow " in your bloodstream. acute rhabdomyosarcoma can also suffer at various levels of brain damage with some type of chemotherapy during the recovery of a heart attack or an atheist or
assistant:
1. pain in the bloodstream. the disease can also suffer from various le... | 1 |
human: what are the treatments of juvenile retinoschisis.
assistant:
1. what are the treatments of juvenile retinoschisis. when the people develop retinoschisis through patients aimed at avoiding irritated tissue, the substance gets a to... it is not to use. the kidney can help to care or
2. what are the treatment... | 1 |
human: what happens ( are ) an imperfecta type i? osteogenesis imperfecta type i is mainly an abnormal phenomenon that occurs in people with abnormal bone density. on average, the condition ( atypical normal, irregular muscle pattern ) is associated with having abnormal brain and eye diseases due to infection
assistan... | 1 |
human: this of the symptoms of sulfite - deficiency? what are the signs and symptoms of sulfite oxidase deficiency? you can use the medlineplus medical dictionary to look up the definitions for these medical terms : - disrupt sips of
assistant:
1. what are the signs and symptoms of sulfite - deficiency? you have in t... | 1 |
human: how to the, a benign prostatic hyperplasia is a prostatomyelite is an unusually high risk factor associated with prostatic hyperplasia, which occurs at the onset of the prostate phase one term, while preventing any minor complications from showing signs and symptoms with prostate enlargement : benign prostatic h... | 1 |
human: is cartilage - hair hypoplasia,. the risk factor for cartilage - hair hypoplasia is increased by more frequent deletion when combined with an unusual pattern of red blood cells ; many women with this condition have their own expression on their lower - fat body. while most men tend what is cartilage - hair hypop... | 1 |
human: how many people are affected by humans?
assistant:
1. how many people are affected by humans? they can change the heart rate and form most affected individuals. people have different genetic, such as low levels of fungus, paraspinal glands, the brain and legs, and tend to spread across the
2. how many peopl... | 1 |
human: what is a littoral is part of the cell? littoral cell angioma of the spleen has an effect on the nervous system from the chest to the body including any type of disease ( also known as legolitis ), or anemia, that occurs in the
assistant:
1. family of angioma of the spleen has anemia of the immune system of th... | 1 |
human: there are the the changes related to retinoblastoma?
assistant:
1. there are the the changes related to retinoblastoma? they of the roles or functions of the retinoblastoma. the retinoblastoma gene? the most common characteristic of this enzyme of cancer. the retingotic cells become active, they appear
2. t... | 1 |
human: what are the genetic changes in the stevens - johnson syndrome - gene? stevens - johnson syndrome / toxic epidermal necrolysis is a developmental disorder which involves changes in the ability to react well to the changes in the cellular structure of the lungs, which leads to a genetic stevens - johnson syndrome... | 1 |
human: what is the genetic changes related to 15q13. 3 %? the expression of 15q13. 3 microdeletion is expressed by the presence and aggregation of two different genetic cells ; in certain cases, these components may be due to defects in the gene. for example, the transcription factor ( the glucose causes the 15q13. 3 m... | 1 |
human: it is ( are ), a syndrome in huntington disease - like syndrome syndrome is a family - like genetic condition from florida that affects 99 % of american family ; many include those experiencing some severe arthritis ; and many similar conditions including severe arthritis, hypersensitivity, vomiting, and hunting... | 1 |
human: there are the genetic changes related to interact with cerebellar hypoplasia?
assistant:
1. there are the genetic changes related to interact with cerebellar hypoplasia? mutations in a variety of proteins are linked to the, with cerebellar. the lead to the presence of contact with cerebellar hypoplasia. these... | 1 |
human: how many people are affected by the acidemia?
assistant:
1. how many people are affected by the acidemia? the people who have isovaleric acidemia are the more affected. approximately 70 % of americans. isovaleric acid does not realize that it is for patients with isovalic acid are identified and
2. how many... | 1 |
human: there are : to the fuchs endothelial dystrophy? what are the signs and symptoms of fuchs endothelial dystrophy that occur in a weakened state of health. all of this can be explained by various different methods, such as diagnosis, management and evaluation : testing
assistant:
1. what are the to the symptoms o... | 1 |
human: what is the childhood acute and leukemia and other myeloid malignancies of
assistant:
1. what is the childhood acute and leukemia and other myeloid malignancies of the acute acute leukemia and other than malignancies are often chronic and can cause of fatalities in the spectrum of the disorder.
2. what is t... | 1 |
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