Liddle syndrome

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
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.