Search Ontology:
Human Disease
autosomal recessive spinocerebellar ataxia 32
- Term ID
- DOID:0070413
- Synonyms
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- 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 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models