autosomal recessive spinocerebellar ataxia 32

Summary
Synonym
  • 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.
Super Class
autosomal recessive cerebellar ataxia
Disease Ontology
DOID:0070413
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
11757 Prdx3 peroxiredoxin 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
64371 Prdx3 peroxiredoxin 3

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024