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- B695e9b993d4ace24ea0a5c19c8d3902f hasDbXref "Orphanet:85201" @default.
- B695e9b993d4ace24ea0a5c19c8d3902f type Axiom @default.
- B695e9b993d4ace24ea0a5c19c8d3902f annotatedProperty IAO_0000115 @default.
- B695e9b993d4ace24ea0a5c19c8d3902f annotatedSource MONDO_0011640 @default.
- B695e9b993d4ace24ea0a5c19c8d3902f annotatedTarget "Genitopatellar syndrome is a rare congenital patellar anomaly syndrome characterized by patellar aplasia or hypoplasia associated with microcephaly, characteristic coarse facial features (microcephaly, bitemporal narrowing, large, broad nose with high nasal bridge, prominent cheeks and micro/retrognathia or prognathism), arthrogryposis of the hips and knees, urogenital abnormalities and intellectual deficiency." @default.