Gene: ABCC9 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9 		0.020 GeneticVariation disease BEFREE We term this channelopathy resulting from loss-of-function of SUR2-containing K<sub>ATP</sub> channels ABCC9-related Intellectual disability Myopathy Syndrome (AIMS). 31575858 2019
Entrez Id: 10060
Gene Symbol: ABCC9
ABCC9 		0.020 GeneticVariation disease BEFREE KATP channelopathies implicated in patients with mechanical and/or electrical heart disease include dilated cardiomyopathy (with ventricular arrhythmia; CMD1O) and adrenergic atrial fibrillation. 20033705 2010