Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hyperaldosteronism, Familial, Type II CLCN2 disease C1854107 CausalMutation 0.61 orphanet , disgenet
Hyperaldosteronism, Familial, Type II CLCN2 disease C1854107 Biomarker 0.61 orphanet , disgenet
Hyperaldosteronism, Familial, Type II CLCN2 disease C1854107 GeneticVariation 0.61 orphanet , disgenet
Hyperaldosteronism, Familial, Type II FAM131A disease C1854107 CausalMutation 0.1 disgenet
Hyperaldosteronism, Familial, Type II PCSK9 disease C1854107 Biomarker 0.02 disgenet
Hyperaldosteronism, Familial, Type II PCSK9 disease C1854107 GeneticVariation 0.02 disgenet
Hyperaldosteronism, Familial, Type II FLNB disease C1854107 Biomarker 0.01 disgenet
Hyperaldosteronism, Familial, Type II RBAK disease C1854107 GeneticVariation 0.01 disgenet
Hyperaldosteronism, Familial, Type II KCNJ5 disease C1854107 GeneticVariation 0.01 disgenet
Hyperaldosteronism, Familial, Type II PMS2 disease C1854107 GeneticVariation 0.01 disgenet
Hyperaldosteronism, Familial, Type II GNA12 disease C1854107 GeneticVariation 0.01 disgenet
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