Oculocutaneous albinism type 3 (Q90689)
From determinar.ia.br - Determine suas informações
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. |
Statements
CID11:ID_1565320806
0 references
dki-india-ID_1565320806
0 references
Concluído
0 references
13 August 2026
0 references
