Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0036572
Disease: Seizures
Seizures 		0.110 CausalMutation CLINVAR A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders. 26938784

2016
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0036572
Disease: Seizures
Seizures 		0.110 Biomarker HPO

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0036572
Disease: Seizures
Seizures 		0.110 GeneticVariation CLINVAR