Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B40e7926d8ebdfb400791a1df7da8a81e> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B40e7926d8ebdfb400791a1df7da8a81e hasDbXref "NCIT:C84522" @default.
- B40e7926d8ebdfb400791a1df7da8a81e type Axiom @default.
- B40e7926d8ebdfb400791a1df7da8a81e annotatedProperty IAO_0000115 @default.
- B40e7926d8ebdfb400791a1df7da8a81e annotatedSource MONDO_0011147 @default.
- B40e7926d8ebdfb400791a1df7da8a81e 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.