Source: UNIPROT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2
CUI: C1854107
Disease: Hyperaldosteronism, Familial, Type II
Hyperaldosteronism, Familial, Type II 		0.610 GeneticVariation UNIPROT A gain-of-function mutation in the CLCN2 chloride channel gene causes primary aldosteronism. 29403012

2018
Entrez Id: 1181
Gene Symbol: CLCN2
CLCN2
CUI: C1854107
Disease: Hyperaldosteronism, Familial, Type II
Hyperaldosteronism, Familial, Type II 		0.610 GeneticVariation UNIPROT CLCN2 chloride channel mutations in familial hyperaldosteronism type II. 29403011

2018