Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc04ad10fbc492f532613f6617cd30d08> ?p ?o ?g. }
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- Bc04ad10fbc492f532613f6617cd30d08 hasDbXref "Orphanet:896" @default.
- Bc04ad10fbc492f532613f6617cd30d08 type Axiom @default.
- Bc04ad10fbc492f532613f6617cd30d08 annotatedProperty IAO_0000115 @default.
- Bc04ad10fbc492f532613f6617cd30d08 annotatedSource MONDO_0007862 @default.
- Bc04ad10fbc492f532613f6617cd30d08 annotatedTarget "Waardenburg syndrome type 3 (WS3) is a very rare subtype of Waardenburg syndrome (WS) that is characterized by limb anomalies in association with congenital hearing loss, minor defects in structures arising from neural crest, resulting in pigmentation anomalies of eyes, hair, and skin." @default.