Griscelli syndrome type 1 (Q100373)
From determinar.ia.br - Determine suas informações
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. |
