Griscelli syndrome type 3 (Q100377): Difference between revisions
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15 August 2026
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Latest 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. |
Statements
CID11:ID_1959052636
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dki-india-ID_1959052636
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Concluído
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15 August 2026
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