Griscelli syndrome type 2 (Q88711)
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This type, caused by mutations in RAB27A presents with pigmentary dilution and immunodeficiency
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1836541365 |
||
| English | Griscelli syndrome type 2 |
This type, caused by mutations in RAB27A presents with pigmentary dilution and immunodeficiency |
Statements
CID11:ID_1836541365
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dki-india-ID_1836541365
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Concluído
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13 August 2026
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