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- Bfc13f985c7c56240a9e6607d397f11e5 hasDbXref "Orphanet:2756" @default.
- Bfc13f985c7c56240a9e6607d397f11e5 type Axiom @default.
- Bfc13f985c7c56240a9e6607d397f11e5 annotatedProperty IAO_0000115 @default.
- Bfc13f985c7c56240a9e6607d397f11e5 annotatedSource MONDO_0008137 @default.
- Bfc13f985c7c56240a9e6607d397f11e5 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.