Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B445c69e4038103977e7f892787ef91b9> ?p ?o ?g. }
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- B445c69e4038103977e7f892787ef91b9 hasDbXref "Orphanet:3440" @default.
- B445c69e4038103977e7f892787ef91b9 type Axiom @default.
- B445c69e4038103977e7f892787ef91b9 annotatedProperty IAO_0000115 @default.
- B445c69e4038103977e7f892787ef91b9 annotatedSource MONDO_0018094 @default.
- B445c69e4038103977e7f892787ef91b9 annotatedTarget "A disorder characterized by varying degrees of deafness and minor defects in structures arising from neural crest, including pigmentation anomalies of eyes, hair, and skin. WS is classified into four clinical and genetic phenotypes." @default.