Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8488321ce2cc44c0c3cdf6c9e84b41c3> ?p ?o ?g. }
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- B8488321ce2cc44c0c3cdf6c9e84b41c3 hasDbXref "Orphanet:53697" @default.
- B8488321ce2cc44c0c3cdf6c9e84b41c3 type Axiom @default.
- B8488321ce2cc44c0c3cdf6c9e84b41c3 annotatedProperty IAO_0000115 @default.
- B8488321ce2cc44c0c3cdf6c9e84b41c3 annotatedSource MONDO_0008151 @default.
- B8488321ce2cc44c0c3cdf6c9e84b41c3 annotatedTarget "Gnathodiaphyseal dysplasia (GDD) is a bone dysplasia characterized by bone fragility, frequent bone fractures at a young age, cemento-osseous lesions of the jaw bones, bowing of tubular bones (tibia and fibula) and diaphyseal sclerosis of long bones associated with generalized osteopenia. GD follows an autosomal dominant mode of transmission." @default.