Oculocutaneous albinism (Q39994): Difference between revisions
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| description / pt-br | description / pt-br | ||
Albinismo oculocutâneo é um transtorno geneticamente heterogêneo caracterizado por pigmentação diminuída ou ausente dos cabelos, pele e olhos. | |||
| description / en | description / en | ||
Oculocutaneous albinism is a genetically heterogeneous congenital disorder characterised by decreased or absent pigmentation in the hair, skin, and eyes. | |||
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. |
