Search Ontology:
Human Disease

spinocerebellar ataxia 4

Term ID
DOID:0050957
Synonyms
  • SCA4
Definition
An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, dysarthria and peripheral neuropathy that has_material_basis_in heterozygous trinucleotide repeat expansion (GGCn) in the ZFHX3 gene on chromosome 16q22. (2)
References
Ontology
Human Disease   ( DOID:0050957 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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