Oculocutaneous albinism type 3 (Q90689): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
OCA3 é causado por uma mutação no gene TYRP1 e é comumente chamado de albinismo oculocutâneo Rufous. Ocorre principalmente na África Subsaariana e é caracterizado por coloração vermelho-acobreada brilhante de pele e cabelos e por diluição da cor das íris. | |||
| description / en | description / en | ||
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. | |||
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. |
