ATP1A3-associated neurological disorder

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
ATP1A3-associated neurological disorder
ATP1A3 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with ATP1A3-associated neurological disorder.
5 View disease cluster →
Capos syndrome 1 shared geneATP1A3 Related via 1 shared gene including ATP1A3. Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss 1 shared geneATP1A3 Related via 1 shared gene including ATP1A3. Alternating hemiplegia of childhood 1 shared geneATP1A3 Related via 1 shared gene including ATP1A3. Congenital epicanthus 1 shared geneATP1A3 Related via 1 shared gene including ATP1A3. Anhedonia 1 shared geneATP1A3 Related via 1 shared gene including ATP1A3.