Griscelli syndrome type 1 (Q100373): Difference between revisions
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Esta síndrome é caracterizada por diluição pigmentar do cabelo e da pele e anormalidades neurológicas primárias resultantes de mutações no gene MYO5A. | |||
| description / en | description / en | ||
This syndrome is characterised by pigmentary dilution of hair and skin and primary neurologic abnormalities resulted from mutations in MYO5A gene. | |||
Revision as of 17:05, 16 August 2026
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 |
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| 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. |
