autosomal recessive ataxia due to PEX10 deficiency

Findings

No curated finding names autosomal recessive ataxia due to PEX10 deficiency yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.

What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.

Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.

Where it sits

A kind of

• autosomal recessive metabolic cerebellar ataxia

Resolves to: autosomal recessive ataxia due to PEX10 deficiency

Also called

mild peroxismal disorder due to PEX10 deficiency