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- Ba2a671f368f8522d2044e30ed0f771c1 hasDbXref "Orphanet:894" @default.
- Ba2a671f368f8522d2044e30ed0f771c1 type Axiom @default.
- Ba2a671f368f8522d2044e30ed0f771c1 annotatedProperty IAO_0000115 @default.
- Ba2a671f368f8522d2044e30ed0f771c1 annotatedSource MONDO_0008670 @default.
- Ba2a671f368f8522d2044e30ed0f771c1 annotatedTarget "Waardenburg syndrome type 1 (WS1) is a subtype of Waardenburg syndrome (WS), disorder characterized by congenital deafness, minor defects in structures arising from neural crest resulting in pigmentation anomalies of eyes, hair, and skin, in combination with dystopia canthorum." @default.