oculocutaneous albinism type 2 (Q2017745)
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oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13
- oculocutaneous albinism type II
- Oculocutaneous Albinism, Tyrosinase-Positive
- OCA2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | oculocutaneous albinism type 2 |
oculocutaneous albinism that has material basis in an autosomal recessive mutation of OCA2 on chromosome 15q12-q13 |
|
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