Oculocutaneous albinism type 1A (Q65037): Difference between revisions
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| Property / Canonical URI: https://id.who.int/icd/entity/1168847652 / rank | |||||||||||||||
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CID11:ID_1168847652 | |||||||||||||||
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dki-india-ID_1168847652 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 12:45, 14 August 2026
OCA-1 is caused by mutation in the tyrosinase gene (TYR). OCA-1A is due to complete absence of TYR and a more severe clinical phenotype than OCA-1B.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1168847652 |
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| English | Oculocutaneous albinism type 1A |
OCA-1 is caused by mutation in the tyrosinase gene (TYR). OCA-1A is due to complete absence of TYR and a more severe clinical phenotype than OCA-1B. |
Statements
CID11:ID_1168847652
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dki-india-ID_1168847652
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Concluído
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13 August 2026
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