Alternating Hemiplegia Of Childhood Gene Set

Dataset	DisGeNET Gene-Disease Associations
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)
External Link	https://www.disgenet.org/browser/0/1/0/C0338488
Similar Terms
Downloads & Tools

Genes

8 genes associated with the disease Alternating Hemiplegia Of Childhood in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ADCY5	adenylate cyclase 5
ATP1A2	ATPase, Na+/K+ transporting, alpha 2 polypeptide
ATP1A3	ATPase, Na+/K+ transporting, alpha 3 polypeptide
CACNA1A	calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
SLC1A3	solute carrier family 1 (glial high affinity glutamate transporter), member 3
SLC2A1	solute carrier family 2 (facilitated glucose transporter), member 1
TANGO2	transport and golgi organization 2 homolog (Drosophila)
TBC1D24	TBC1 domain family, member 24