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

• OMIM:619862

Ontology

Human Disease   ( DOID:0070413 )