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Metadata
ID DOID:0050957
Name spinocerebellar ataxia type 4
Definition An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene.
https://rarediseases.info.nih.gov/diseases/9970/spinocerebellar-ataxia-4
Xrefs

GARD:9970

MESH:D020754

OMIM:600223

ORDO:98765

SNOMEDCT_US_2020_09_01:715755008

UMLS_CUI:C0752122

Parent Relationships

is_a autosomal dominant cerebellar ataxia

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