Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.100 GeneticVariation CLINVAR Alternating hemiplegia of childhood. 8496742

1993
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		0.100 GeneticVariation CLINVAR Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes. 2842249

1988