Oculocutaneous albinism (Q39994): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Linked ICD 10 | |||
| Property / Linked ICD 10: E70.3 / rank | |||
Normal rank | |||
Latest revision as of 05:37, 13 August 2026
Oculocutaneous albinism is a genetically heterogeneous congenital disorder characterised by decreased or absent pigmentation in the hair, skin, and eyes.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | EC23.20 |
||
| English | Oculocutaneous albinism |
Oculocutaneous albinism is a genetically heterogeneous congenital disorder characterised by decreased or absent pigmentation in the hair, skin, and eyes. |
Statements
CID11:EC23.20
0 references
dki-india-EC23.20
0 references
Concluído
0 references
13 August 2026
0 references
