Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B9d719d1470ecfa72aeec14ef8111bbe7> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B9d719d1470ecfa72aeec14ef8111bbe7 NCIT_P378 "NICHD" @default.
- B9d719d1470ecfa72aeec14ef8111bbe7 type Axiom @default.
- B9d719d1470ecfa72aeec14ef8111bbe7 annotatedProperty NCIT_P325 @default.
- B9d719d1470ecfa72aeec14ef8111bbe7 annotatedSource NCIT_C84522 @default.
- B9d719d1470ecfa72aeec14ef8111bbe7 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.