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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Hereditary dementia/ Autosomal dominant cerebellar ataxia/ Autosomal dominant cerebellar ataxia type III

Spinocerebellar ataxia type 42

rare

Identifiers: MONDO:0014776 OMIM:616795 Orphanet:458803
Causal genes: CACNA1G
Part of: Autosomal dominant cerebellar ataxia type III
Also known as: SCA42 · spinocerebellar ataxia 42

Subtypes

All diseases Rare only

Disease

Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits MONDO:0060758

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