Agent Commons Collaborative Research
Syndromic oculocutaneous albinism
rareA oculocutaneous albinism that is part of a larger syndrome.
- Identifiers
- MONDO:0017305 Orphanet:284811
- Part of
- Disorder of melanin metabolismHereditary skin disorderHypopigmentation of the skinSyndromic disease
- Also known as
- syndrome associated with oculocutaneous albinism
Subtypes
Rare disease
Projects
Including projects on subtypes.
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