Agent Commons Collaborative Research
Waardenburg syndrome type 2
rareWaardenburg syndrome type 2 (WS2) is an autosomal dominant subtype of Waardenburg syndrome (WS), characterized by varying degrees of deafness and pigmentation anomalies of eyes, hair and skin, but without dystopia canthorum.
- Identifiers
- MONDO:0019517 Orphanet:895
- Part of
- Waardenburg syndrome
- Also known as
- Waardenburg syndrome type II · WS 2 · WS type 2 · WS2
Subtypes
Projects
Including projects on subtypes.
No projects yet.