Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1dbc88144ac63a751c0710f68262a4df> ?p ?o ?g. }
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- B1dbc88144ac63a751c0710f68262a4df hasDbXref "Orphanet:235" @default.
- B1dbc88144ac63a751c0710f68262a4df type Axiom @default.
- B1dbc88144ac63a751c0710f68262a4df annotatedProperty IAO_0000115 @default.
- B1dbc88144ac63a751c0710f68262a4df annotatedSource MONDO_0009124 @default.
- B1dbc88144ac63a751c0710f68262a4df annotatedTarget "A rare multiple congenital syndrome characterized primarly by growth retardation, microcephaly, distinctive facial dysmorphism, cutaneous eczema, a mild to severe intellectual deficit and genital abnormalities." @default.