Short qt syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
SHORT QT SYNDROME
C2348199MONDO:0000453
CACNA1C Unknown — ClinGen, Disgenet, GenCC
CACNA2D1 Unknown
21383000
ClinGen, Disgenet
CACNB2 Unknown — Disgenet
KCNQ1 Unknown
15159330 16109388 24380499 24818999 25974115 26168993 26279191 26346102 28491547 28491751 29213224 8528244 8900283
ClinGen, Disgenet, GWAS catalog
SCN5A Unknown — Disgenet
SLC22A5 Unknown — ClinGen, Disgenet
SLC4A3 Unknown
29167417
ClinGen, ClinVar, Disgenet
TRPM4 Unknown — Disgenet
VCL Unknown — Disgenet
SHORT QT SYNDROME 1
609620C1865020MESH:C566506
KCNH2 Unknown
18724381 29574456
CTD, Disgenet, HPO
KCNJ2 Unknown — Disgenet
KCNQ1 Unknown — Disgenet
SHORT QT SYNDROME 2
C1865019609621MESH:C566505
KCNH2 Unknown — Disgenet
KCNJ2 Unknown — Disgenet
KCNQ1 Unknown — CTD, Disgenet, HPO
SHORT QT SYNDROME 3
C1865018609622MESH:C566504
KCNH2 Unknown — Disgenet
KCNJ2 Unknown — CTD, Disgenet, HPO
KCNQ1 Unknown — Disgenet
All11 Causal4 Unknown11
Related Diseases Diseases that share the most curated genes with Short qt syndrome.
5 View disease cluster →
Congenital short qt syndrome 5 shared genesKCNJ2, KCNH2, KCNQ1, CACNA2D1, SLC4A3 Related via 5 shared genes including KCNJ2, KCNH2, KCNQ1. Long qt syndrome, digenic 3 shared genesKCNH2, KCNQ1, SCN5A Related via 3 shared genes including KCNH2, KCNQ1, SCN5A. Ventricular fibrillation 8 shared genesCACNB2, TRPM4, KCNJ2, CACNA1C, KCNH2, SCN5A, CACNA2D1, VCL Related via 8 shared genes including CACNB2, TRPM4, KCNJ2. Cardiac conduction disease 3 shared genesCACNB2, TRPM4, SCN5A Related via 3 shared genes including CACNB2, TRPM4, SCN5A. Conduction disorder of the heart 5 shared genesTRPM4, CACNA1C, KCNH2, KCNQ1, SCN5A Related via 5 shared genes including TRPM4, CACNA1C, KCNH2.