Griscelli syndrome type 1 (Q100373)
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This syndrome is characterised by pigmentary dilution of hair and skin and primary neurologic abnormalities resulted from mutations in MYO5A gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_875700770 |
||
| English | Griscelli syndrome type 1 |
This syndrome is characterised by pigmentary dilution of hair and skin and primary neurologic abnormalities resulted from mutations in MYO5A gene. |
Statements
CID11:ID_875700770
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dki-india-ID_875700770
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Concluído
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15 August 2026
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