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Metadata
ID	DOID:0050969
Name	spinocerebellar ataxia type 18
Definition	An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23. https://rarediseases.info.nih.gov/diseases/9976/spinocerebellar-ataxia-18
Xrefs	GARD:9976 OMIM:607458
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia