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- Be61258d9d581cae98813d2e134063fbc hasDbXref "Orphanet:2756" @default.
- Be61258d9d581cae98813d2e134063fbc type Axiom @default.
- Be61258d9d581cae98813d2e134063fbc annotatedProperty IAO_0000115 @default.
- Be61258d9d581cae98813d2e134063fbc annotatedSource MONDO_0008137 @default.
- Be61258d9d581cae98813d2e134063fbc annotatedTarget "Oral-facial-digital syndrome, type 10 is characterized by facial (telecanthus, flat nasal bridge, retrognathia), oral (cleft palate, vestibular frenula) and digital (oligodactyly, preaxial polydactyly) features, associated with remarkable radial shortening, fibular agenesis and coalescence of tarsal bones. The syndrome has been described in one 10-month-old girl. No new cases have been described since 1993." @default.