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Human Disease

autosomal recessive spinocerebellar ataxia 24

Term ID
DOID:0111615
Synonyms
  • SCAR24
Definition
An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/26872069
References
Ontology
Human Disease   ( DOID:0111615 )
Relationships
is a type of
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Genes Involved
Zebrafish Models