Griscelli syndrome type 3 (Q100377): Difference between revisions
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| description / pt-br | description / pt-br | ||
Este tipo, causado por mutações nos genes MLPH ou MYO5A, apresenta-se apenas com hipopigmentação. | |||
| description / en | description / en | ||
This type, caused by mutations in MLPH or MYO5A genes, presents with hypopigmentation alone. | |||
Revision as of 17:05, 16 August 2026
This type, caused by mutations in MLPH or MYO5A genes, presents with hypopigmentation alone.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1959052636 |
||
| English | Griscelli syndrome type 3 |
This type, caused by mutations in MLPH or MYO5A genes, presents with hypopigmentation alone. |
