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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00725 | Short QT syndrome | Short QT syndrome (SQTS) is a cardiovascular disorder resulting from mutations in cardiac ion channels. The mutation of genes (KCNH2, KCNQ1, and KCNJ2) encoding for cardiac potassium channels plays a central ... | Cardiovascular disease |
(SQT1) KCNH2 [HSA:3757] [KO:K04905] (SQT2) KCNQ1 [HSA:3784] [KO:K04926] (SQT3) KCNJ2 [HSA:3759] [KO:K04996] (SQT7) SLC4A3 [HSA:6508] [KO:K13856] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |