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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Autosomal genetic disease/ Autosomal recessive disease/ Autosomal recessive cerebellar ataxia/ Autosomal recessive metabolic cerebellar ataxia

Autosomal recessive ataxia due to PEX10 deficiency

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Identifiers: MONDO:0016614 Orphanet:247815
Causal genes: PEX10
Part of: Autosomal recessive metabolic cerebellar ataxia
Also known as: mild peroxismal disorder due to PEX10 deficiency

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