Liddle syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
LIDDLE SYNDROME
C0221043MESH:D056929526MONDO:0008323
REN Unknown
12185466
CTD, Disgenet
SCNN1A Unknown
23348737 28710092
CTD, Disgenet, GenCC, Orphanet
SCNN1B Unknown
18398334 19344079
CTD, Disgenet, GenCC, Orphanet
SCNN1G Unknown
10074483 11228173 17634077 21775436 26075967 30977777 31655555 32161960 7550319 7777572 7806569 8986818 9114818
ClinGen, Disgenet, GWAS catalog, Orphanet
LIDDLE SYNDROME 1
177200MONDO:0020607
SCNN1B Causal
8589714 9100575 15483078
ClinVar, GenCC, HPO
LIDDLE SYNDROME 2
618114C4748251MONDO:0020854
SCNN1G Causal
7550319 26537344
ClinVar, Disgenet, GenCC, HPO, ClinGen
LIDDLE SYNDROME 3
618126C4748292MONDO:0029132
SCNN1A Causal — ClinVar, Disgenet, GenCC, HPO
All4 Causal3 Unknown4
Related Diseases Diseases that share the most curated genes with Liddle syndrome.
5 View disease cluster →
renal tubular dysgenesis of genetic origin 1 shared geneREN Related via 1 shared gene including REN. Pseudohypoparathyroidism 3 shared genesSCNN1A, SCNN1B, SCNN1G Related via 3 shared genes including SCNN1A, SCNN1B, SCNN1G. pseudohypoaldosteronism, type IB1, autosomal recessive 1 shared geneSCNN1A Related via 1 shared gene including SCNN1A. Juvenile hyperuricemic nephropathy 1 shared geneREN Related via 1 shared gene including REN. Tonne-kalscheuer syndrome 1 shared geneREN Related via 1 shared gene including REN.