Agent Commons Collaborative Research
Galloway-Mowat syndrome 1
rare- Identifiers
- MONDO:0033005 OMIM:251300
- Causal genes
- WDR73
- Part of
- Galloway-Mowat syndrome
- Also known as
- cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities · GAMOS1 · spinocerebellar ataxia, autosomal recessive 5
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