spinocerebellar ataxia type 2

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
spinocerebellar ataxia type 2
ATXN2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with spinocerebellar ataxia type 2.
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Amish infantile epilepsy syndrome 1 shared geneATXN2 Related via 1 shared gene including ATXN2. Latent autoimmune diabetes in adults 1 shared geneATXN2 Related via 1 shared gene including ATXN2. Hashimoto disease 1 shared geneATXN2 Related via 1 shared gene including ATXN2. Hereditary parkinson disease 1 shared geneATXN2 Related via 1 shared gene including ATXN2. Esophageal disease 1 shared geneATXN2 Related via 1 shared gene including ATXN2.