alternating hemiplegia of childhood Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A hemiplegia characterized by recurrent episodes of temporary weakness or complete paralysis on one or both sides of the body. (Human Disease Ontology, DOID_0050635)
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Genes

2 genes involed in the disease alternating hemiplegia of childhood from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide