Oculocutaneous albinism type 3 (Q90689): Difference between revisions
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Revision as of 17:40, 15 August 2026
OCA3 is caused by a mutation in the TYRP1 gene and is commonly called rufous oculocutaneous albinism (ROCA). It occurs principally in Sub-Saharan Africa and is characterised by bright copper-red colouration of the skin and hair and by dilution of the colour of the irides.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1565320806 |
||
| English | Oculocutaneous albinism type 3 |
OCA3 is caused by a mutation in the TYRP1 gene and is commonly called rufous oculocutaneous albinism (ROCA). It occurs principally in Sub-Saharan Africa and is characterised by bright copper-red colouration of the skin and hair and by dilution of the colour of the irides. |
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CID11:ID_1565320806
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dki-india-ID_1565320806
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