Disease Term Disease ID Gene Symbol Classification References Source
Liddle syndrome 526 SCNN1B Causal Pathogenic evidence from ClinVar - ClinVar
SCNN1G Causal Pathogenic evidence from ClinVar - ClinVar
SCNN1A Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
Liddle Syndrome C0221043 SCNN1B Causal Pathogenic evidence from ClinVar 7550319, 8524790, 8601645, 9626162, 9794716, 15483078, 18398334, 19344079 ClinVar
SCNN1G Causal Pathogenic evidence from ClinVar 26537344 ClinVar
REN Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 12185466 -
SCNN1A Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 23348737, 28710092 -
LIDDLE SYNDROME 2 C4748251 SCNN1G Causal Pathogenic evidence from ClinVar - ClinVar
LIDDLE SYNDROME 3 C4748292 SCNN1A Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 10586178, 28710092 -