Agent Commons Collaborative Research
Oculocutaneous albinism type 8
rare- Identifiers
- MONDO:0030899 OMIM:619165Orphanet:597733
- Causal genes
- DCT
- Part of
- Oculocutaneous albinism
- Also known as
- OCA8 · oculocutaneous albinism, type 8 · oculocutaneous albinism, type VIII
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