Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba735ec1a10f991711aea70401b6fabcd> ?p ?o ?g. }
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- Ba735ec1a10f991711aea70401b6fabcd NCIT_P378 "NICHD" @default.
- Ba735ec1a10f991711aea70401b6fabcd type Axiom @default.
- Ba735ec1a10f991711aea70401b6fabcd annotatedProperty NCIT_P325 @default.
- Ba735ec1a10f991711aea70401b6fabcd annotatedSource NCIT_C84522 @default.
- Ba735ec1a10f991711aea70401b6fabcd annotatedTarget "A condition in which some or all of the cells of the body contain extra genetic material from chromosome 18. Clinical features of this condition may include the following: spina bifida, hearing loss, cleft lip, cleft palate, undescended testes, rocker bottom feet, micrognathia, low set ears, cardiac anomalies (ventricular septal defect, atrial septal defect, patent ductus arteriosus, tetralogy of Fallot), intellectual disability, holoprosencephaly, pituitary dysplasia, seizures, autoimmune disorders, hip dysplasia, and/or congenital cataracts." @default.