Spinocerebellar ataxia type 42

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Subtype of: Spinocerebellar ataxia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
spinocerebellar ataxia type 42
MONDO_0014776
CACNA1G Causal
17397049 21937992 24896178 25558065 26350204 26456284 26715324 28726809 29878067
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Spinocerebellar ataxia type 42.
5 View disease cluster →
Developmental disorder with hypotonia, epilepsy, and cerebral/cerebellar atrophy 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Autosomal recessive mental retardation 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Spastic ataxia 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Spinocerebellar ataxia 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G.