Albinism or other specified genetically-determined hypomelanotic disorders (Q39993): Difference between revisions
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| description / pt-br | description / pt-br | ||
Grande grupo de transtornos hereditários em que a produção cutânea de melanina está reduzida ou ausente, principalmente como resultado de defeitos em enzimas necessárias para a biossíntese normal de melanina. | |||
| description / en | description / en | ||
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. | |||
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 |
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| 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. |
