Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits

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Subtype of: Spinocerebellar ataxia · Spinocerebellar ataxia type 42
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits
MONDO_0060758
CACNA1G Causal
29878067
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits.
5 View disease cluster →
Spinocerebellar ataxia type 42 1 shared geneCACNA1G Related via 1 shared gene including CACNA1G. Developmental disorder with hypotonia, epilepsy, and cerebral/cerebellar atrophy 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.