Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B45031ec811a56611085c85c2fb27b6bc> ?p ?o ?g. }
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- B45031ec811a56611085c85c2fb27b6bc hasDbXref "Orphanet:235" @default.
- B45031ec811a56611085c85c2fb27b6bc type Axiom @default.
- B45031ec811a56611085c85c2fb27b6bc annotatedProperty IAO_0000115 @default.
- B45031ec811a56611085c85c2fb27b6bc annotatedSource MONDO_0009124 @default.
- B45031ec811a56611085c85c2fb27b6bc 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.