Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B2435c40e29c5c33488cedbff762ed1d7> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B2435c40e29c5c33488cedbff762ed1d7 hasDbXref "Orphanet:3269" @default.
- B2435c40e29c5c33488cedbff762ed1d7 type Axiom @default.
- B2435c40e29c5c33488cedbff762ed1d7 annotatedProperty IAO_0000115 @default.
- B2435c40e29c5c33488cedbff762ed1d7 annotatedSource MONDO_0017985 @default.
- B2435c40e29c5c33488cedbff762ed1d7 annotatedTarget "Congenital radioulnar synostosis is a rare bone disorder that may be isolated or associated with other disorders and that is characterized by failure of segmentation of the radius and ulna during embryological development, causing limited rotational movements of the forearm, which may lead to difficulties with some activities of daily living." @default.