Split (1)

train · 21.6M rows

CUI1 stringlengths 8 8	RELA stringlengths 3 54	CUI2 stringlengths 8 8	Name1 stringlengths 1 2.86k ⌀	Name2 stringlengths 1 2.86k ⌀	Def1 stringlengths 1 8.95k ⌀	Def2 stringlengths 1 8.95k ⌀
C0000768	associated_with	C0266319	Congenital Abnormality	Congenital anomaly of ureter	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266334	Congenital Abnormality	Displaced ureteric orifice	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266335	Congenital Abnormality	Congenital anomaly of urinary bladder	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266342	Congenital Abnormality	Congenital anomaly of urethra	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266361	Congenital Abnormality	Hermaphroditism, True	Malformations of organs or body parts during development in utero.	An historical term for conditions of sexual ambiguity in which the individual possesses gonadal tissues of both sexes.
C0000768	associated_with	C0266365	Congenital Abnormality	Congenital anomaly of female genital system	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266367	Congenital Abnormality	deformity; genital organs, female, congenital, external	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266383	Congenital Abnormality	Uterine Anomalies	Malformations of organs or body parts during development in utero.	An abnormality of the uterus. [https://orcid.org/0000-0002-0736-9199]
C0000768	associated_with	C0266387	Congenital Abnormality	Bicornuate uterus	Malformations of organs or body parts during development in utero.	A congenital uterine anomaly in which the UTERUS is divided into two uterine horns with a significant cleft at the uterine fundus due to partial fusion of the MULLERIAN DUCTS. Bicornuate uterus is sometimes associated with a longitudinal vaginal septum and abnormal development of renal tracts.
C0000768	associated_with	C0266403	Congenital Abnormality	Congenital anomaly of cervix	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266415	Congenital Abnormality	Congenital anomaly of vulva	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266421	Congenital Abnormality	Congenital anomaly of male genital system	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266423	Congenital Abnormality	Congenital anomaly of testis	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266433	Congenital Abnormality	Congenital anomaly of penis	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266438	Congenital Abnormality	Paraspadias	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266439	Congenital Abnormality	Congenital anomaly of prostate	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266441	Congenital Abnormality	Congenital anomaly of spermatic cord	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266443	Congenital Abnormality	Congenital anomaly of vas deferens	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266449	Congenital Abnormality	Congenital anomaly of brain	Malformations of organs or body parts during development in utero.	<p>Most brain malformations begin long before a baby is born. Something damages the developing nervous system or causes it to develop abnormally. Sometimes it's a genetic problem. In other cases, exposure to certain <a href="https://medlineplus.gov/pregnancyandmedicines.html">medicines</a>, <a href="https://medlineplus...
C0000768	associated_with	C0266451	Congenital Abnormality	Cerebral cortical dysgenesis	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266464	Congenital Abnormality	Polymicrogyria	Malformations of organs or body parts during development in utero.	Heterogeneous disorders of cortical malformation characterized by excessive and small fused gyri and shallow sulci of the CORTEX with abnormal cortical lamination. It is considered a malformation secondary to abnormal post-migrational development of the neurons during cerebral cortical development and is associated wit...
C0000768	associated_with	C0266474	Congenital Abnormality	Aqueduct of Sylvius anomaly	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266488	Congenital Abnormality	Ulegyria	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266498	Congenital Abnormality	Congenital anomaly of spinal cord	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266513	Congenital Abnormality	development; defective, congenital, cauda equina	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266515	Congenital Abnormality	Congenital anomaly of spinal meninges	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266516	Congenital Abnormality	Congenital anomaly of the peripheral nervous system	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266517	Congenital Abnormality	Congenital anomaly of peripheral nerve	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266546	Congenital Abnormality	Congenital anomaly of anterior chamber of eye	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266548	Congenital Abnormality	Axenfeld anomaly (disorder)	Malformations of organs or body parts during development in utero.	A rare, congenital, ocular defect caused by anterior segment dysgenesis and characterized by anteriorly displaced Schwalbe's line and iris bands extending into the cornea. In contrast, Rieger's anomaly includes characteristic iris and pupil anomalies.
C0000768	associated_with	C0266554	Congenital Abnormality	Congenital anomaly of sclera	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266563	Congenital Abnormality	Congenital anomaly of macula	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266564	Congenital Abnormality	Congenital anomaly of retina	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266566	Congenital Abnormality	Optic disc structural anomaly	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266572	Congenital Abnormality	Congenital structural abnormality of eyelid	Malformations of organs or body parts during development in utero.	The abnormal formation of the eyelid that is present at the time of birth.
C0000768	associated_with	C0266581	Congenital Abnormality	Congenital anomaly of lacrimal system	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266583	Congenital Abnormality	Congenital anomaly of lacrimal gland	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266587	Congenital Abnormality	Congenital structural abnormality of orbit	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266589	Congenital Abnormality	Congenital ear anomaly NOS (disorder)	Malformations of organs or body parts during development in utero.	An abnormality of the ear. [https://orcid.org/0000-0002-0736-9199]
C0000768	associated_with	C0266592	Congenital Abnormality	Congenital anomaly of ear with impairment of hearing	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266599	Congenital Abnormality	Congenital anomaly of middle ear	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266605	Congenital Abnormality	Congenital anomaly of membranous labyrinth	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266608	Congenital Abnormality	Congenital anomaly of organ of Corti	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266614	Congenital Abnormality	Lop ear	Malformations of organs or body parts during development in utero.	Anterior and inferior folding of the upper portion of the ear that obliterates triangular fossa and scapha. [https://orcid.org/0000-0002-0736-9199, PMID:19152421]
C0000768	associated_with	C0266615	Congenital Abnormality	Darwin's tubercle	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266617	Congenital Abnormality	Congenital anomaly of face	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266619	Congenital Abnormality	Potter's facies	Malformations of organs or body parts during development in utero.	A facial appearance characteristic of a fetus or neonate due to oligohydramnios experienced in the womb, comprising ocular hypertelorism, low-set ears, receding chin, and flattening of the nose. [https://orcid.org/0000-0002-0736-9199]
C0000768	associated_with	C0266623	Congenital Abnormality	Congenital anomaly of neck	Malformations of organs or body parts during development in utero.	An abnormality of the neck. [https://orcid.org/0000-0002-0736-9199]
C0000768	associated_with	C0266629	Congenital Abnormality	Congenital anomaly of the hematopoietic system	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266647	Congenital Abnormality	Congenital anomalies of fetus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266648	Congenital Abnormality	Blighted ovum	Malformations of organs or body parts during development in utero.	Pregnancy loss with visible gestational sac or yolk sac or both but no visible embryo on ultrasonogram.
C0000768	associated_with	C0266652	Congenital Abnormality	abnormal fetus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266656	Congenital Abnormality	Frog fetus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266658	Congenital Abnormality	Autositic twin of asymmetrical conjoined twins	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266659	Congenital Abnormality	Parasitic twin of asymmetrical conjoined twins	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266660	Congenital Abnormality	Triplet monster, NOS	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266661	Congenital Abnormality	Polysomatous monster, NOS	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266665	Congenital Abnormality	Single monster, NOS	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266667	Congenital Abnormality	Cyclocephaly	Malformations of organs or body parts during development in utero.	A rare congenital abnormality characterized by the failure of the embryonic prosencephalon to separate the eye orbit into two distinct cavities. Facial features tend to be absent although a proboscis has been seen to develop in conjunction.
C0000768	associated_with	C0266668	Congenital Abnormality	Cyclops hypognathus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266669	Congenital Abnormality	Opocephalus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266673	Congenital Abnormality	Monster with cranial anomalies, NOS	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266674	Congenital Abnormality	Cranial duplication	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266676	Congenital Abnormality	Agnathus (disorder)	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266677	Congenital Abnormality	Synotus	Malformations of organs or body parts during development in utero.	A congenital malformation characterized by the union or approximation of the ears in front of the neck, often accompanied by the absence or defective development of the lower jaw. [https://orcid.org/0009-0006-4530-3154]
C0000768	associated_with	C0266678	Congenital Abnormality	Derencephalus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266679	Congenital Abnormality	Cebocephaly	Malformations of organs or body parts during development in utero.	A congenital abnormality characterized by a malformation of the head. The eyes are hypoteleric and the nose may be absent or misshapen (small, flattened, single nostril) and defective.
C0000768	associated_with	C0266680	Congenital Abnormality	Ethmocephalus	Malformations of organs or body parts during development in utero.	Ethmocephaly is the rarest form of holoprosencephaly, which occurs due to an incomplete cleavage of the forebrain. Clinically, the disease presents with a proboscis, hypotelorism, microphthalmos and malformed ears. [https://orcid.org/0000-0002-0003-6754, PMID:23248551]
C0000768	associated_with	C0266681	Congenital Abnormality	Omocephalus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266682	Congenital Abnormality	Celosomus	Malformations of organs or body parts during development in utero.	Congenital protrusion of the abdominal or thoracic viscera, usually with a defect of the sternum and ribs as well as of the abdominal walls. [https://orcid.org/0009-0006-4530-3154]
C0000768	associated_with	C0266684	Congenital Abnormality	Fetus in fetu	Malformations of organs or body parts during development in utero.	Rare abnormality where a fetal part of an identical twin that stopped developing during gestation is found within a normally developing fetus. It is considered a TWIN PREGNANCY complication.
C0000768	associated_with	C0266686	Congenital Abnormality	Anadidymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266687	Congenital Abnormality	Cephalodymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266688	Congenital Abnormality	Dipygus	Malformations of organs or body parts during development in utero.	Caudal duplication (CD) is a rare developmental anomaly in which structures derived from the embryonic cloaca and notochord are duplicated to varying extents.
C0000768	associated_with	C0266689	Congenital Abnormality	Cephalothoracopagus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266690	Congenital Abnormality	Thoracodelphus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266691	Congenital Abnormality	Pygodidymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266692	Congenital Abnormality	Craniopagus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266693	Congenital Abnormality	Craniopagus occipitalis	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266694	Congenital Abnormality	Craniopagus parietalis	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266695	Congenital Abnormality	Monocephalus (disorder)	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266696	Congenital Abnormality	Monocephalus tetrapus dibrachius	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266697	Congenital Abnormality	Monocephalus tripus dibrachius	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266698	Congenital Abnormality	Syncephalus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266699	Congenital Abnormality	Deradelphus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266700	Congenital Abnormality	Janiceps (disorder)	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266701	Congenital Abnormality	Anakatadidymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266702	Congenital Abnormality	Gastrothoracopagus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266703	Congenital Abnormality	Thoracodidymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266704	Congenital Abnormality	Thoracopagus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266705	Congenital Abnormality	Thoracopagus parasiticus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266706	Congenital Abnormality	Thoracopagus epigastricus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266707	Congenital Abnormality	Thoracoparacephalus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266709	Congenital Abnormality	Omphaloangiopagus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266711	Congenital Abnormality	Pygopagus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266712	Congenital Abnormality	Katadidymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266713	Congenital Abnormality	Heterodymus	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266714	Congenital Abnormality	Dicephalus dipus tetrabrachius	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266715	Congenital Abnormality	Dicephalus dipus tribrachius	Malformations of organs or body parts during development in utero.	null
C0000768	associated_with	C0266716	Congenital Abnormality	Dicephalus tripus tribrachius	Malformations of organs or body parts during development in utero.	null

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