Oculocutaneous albinism type 2 (Q90683): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_2019316252 | |||
| Property / Canary Token: dki-india-ID_2019316252 / rank | |||
Normal rank | |||
Revision as of 17:40, 15 August 2026
OCA-2 is caused by mutations in the OCA2 (P) gene. Affected individuals have pigmented hair at birth and may develop iris pigmentation, pigmented melanocytic naevi and freckles later in life.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2019316252 |
||
| English | Oculocutaneous albinism type 2 |
OCA-2 is caused by mutations in the OCA2 (P) gene. Affected individuals have pigmented hair at birth and may develop iris pigmentation, pigmented melanocytic naevi and freckles later in life. |
Statements
CID11:ID_2019316252
0 references
dki-india-ID_2019316252
0 references
