| DISEASE NAME | Familial long QT syndrome |
| DISEASE CATEGORY (ICD10) | Diseases of the circulatory system |
| DISEASE ID (ICD10) | I45.8 |
| DISEASE ID (OMIM) | 618447; 611820; 612347; 612955; 613485; 613688; 613693; 613695; 616247; 616249; 192500; 220400; 600919; 601005; 603830; 611818; 611819 |
| 25 combinations linked to 768 | OLI096; OLI218; OLI361; OLI362; OLI363; OLI364; OLI445; OLI459; OLI549; OLI550; OLI551; OLI985; OLI1216; OLI1217; OLI1218; OLI1219; OLI1220; OLI1221; OLI1222; OLI1223; OLI1224; OLI1225; OLI1226; OLI1227; OLI1228 |
| 10 gene combinations linked to 768 | KCNQ1; SCN5A; KCNH2; KCNQ1; CAV3; KCNH2; KCNE1; KCNH2; KCNQ1; KCNE2; KCNH2; KCNE1; KCNH2; KCNH2; SCN5A; KCNE2; SCN5A; KCNE1; KCNQ1; KCNE1; SCN5A |
| ORPHANET ID | 768 |