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Human Disease

autosomal recessive spinocerebellar ataxia 32

Term ID
DOID:0070413
Synonyms
  • SCAR32
Definition
An autosomal recessive cerebellar ataxia characterized by onset of gait ataxia in the second or third decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the PRDX3 gene on chromosome 10q26. https://pubmed.ncbi.nlm.nih.gov/33889951/
References
Ontology
Human Disease   ( DOID:0070413 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models