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Diseases / Metabolic disease/ Inborn errors of metabolism/ DNA repair disease

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy

rare

Identifiers: MONDO:0020771
Part of: DNA repair disease Autosomal recessive cerebellar ataxia
Also known as: SCAN

Subtypes

All diseases Rare only

Disease

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1 MONDO:0011801 TDP1
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 MONDO:0018996 SETX
Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3 MONDO:0020770 COA7

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