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Metadata
ID	DOID:0050974
Name	spinocerebellar ataxia type 25
Definition	An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21. https://rarediseases.info.nih.gov/diseases/9996/spinocerebellar-ataxia-25
Xrefs	GARD:9996 MESH:C537202 MIM:608703
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant cerebellar ataxia