Oculocutaneous albinism (Q39994)
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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
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dki-india-EC23.20
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Concluído
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13 August 2026
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