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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

OMIM:608703

Subsets

DO_rare_slim

Parent Relationships

is_a autosomal dominant cerebellar ataxia

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