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Human Disease

autosomal recessive spinocerebellar ataxia 6

Term ID
DOID:0111617
Synonyms
  • autosomal recessive spinocerebellar ataxia type 6
  • infantile-onset autosomal recessive nonprogressive cerebellar ataxia
  • SCAR6
Definition
An autosomal recessive cerebellar ataxia characterized by onset in infancy of nonprogressive cerebellar ataxia without intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 20q11-q13. (2)
References
Ontology
Human Disease   ( DOID:0111617 )
Relationships
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Genes Involved
Zebrafish Models