Albinism or other specified genetically-determined hypomelanotic disorders (Q39993): Difference between revisions
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13 August 2026
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Revision as of 05:37, 13 August 2026
A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | EC23.2 |
||
| English | Albinism or other specified genetically-determined hypomelanotic disorders |
A large group of heritable disorders in which cutaneous melanin production is reduced or absent, mainly as the result of defects in enzymes required for normal melanin biosynthesis. |
Statements
CID11:EC23.2
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dki-india-EC23.2
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Concluído
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13 August 2026
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