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spinocerebellar ataxia type 4

Disease Summary
Associated Targets (35)
Tbio

25

Tchem

7

Tclin

2

Tdark

1


GARD Rare
Mondo Description Spinocerebellar ataxia type 4 (SCA4) is a very rare progressive and untreatable subtype of type I autosomal dominant cerebellar ataxia (ADCA type I) characterized by ataxia with sensory neuropathy.
Disease Ontology Description An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene.
Mondo Term and Equivalent IDs
MONDO:0010847:  spinocerebellar ataxia type 4
GARD:0009970: 
Orphanet:98765: 
SCTID:715755008: 
UMLS:C0752122: