alternating hemiplegia of childhood Gene Set

Dataset DISEASES Text-mining 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

14 genes co-occuring with the disease alternating hemiplegia of childhood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide 2.88937
NR0B1 nuclear receptor subfamily 0, group B, member 1 2.86409
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide 1.79796
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit 1.34548
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 1.16307
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3 1.08957
TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) 0.953273
PRRT2 proline-rich transmembrane protein 2 0.785574
CR2 complement component (3d/Epstein Barr virus) receptor 2 0.60147
ATP11A ATPase, class VI, type 11A 0.521117
SLC1A3 solute carrier family 1 (glial high affinity glutamate transporter), member 3 0.485125
DNAH8 dynein, axonemal, heavy chain 8 0.412031
SCN1A sodium channel, voltage gated, type I alpha subunit 0.33651
CD63 CD63 molecule 0.291898