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- B670ac4dd6788d2d2c269eb6540136781 hasDbXref "Orphanet:65798" @default.
- B670ac4dd6788d2d2c269eb6540136781 type Axiom @default.
- B670ac4dd6788d2d2c269eb6540136781 annotatedProperty IAO_0000115 @default.
- B670ac4dd6788d2d2c269eb6540136781 annotatedSource MONDO_0008711 @default.
- B670ac4dd6788d2d2c269eb6540136781 annotatedTarget "Goodman syndrome is an extremely rare genetic disorder characterized by marked malformations of the head and face (essentially acrocephaly), abnormalities of the hands and feet (polydactyly, syndactyly, clinodactyly, camptodactyly, ulnar deviation), and congenital heart disease. There have been no further descriptions in the literature since 1979. Goodman syndrome could be a variant of Carpenter syndrome." @default.