Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | AKAP9 CL E G H | 10142 | 379 | OMIM:611820 | Long QT syndrome 11 | | | | 289 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | AKAP9 CL E G H | 10142 | 379 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 289 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | ALG10B CL E G H | 144245 | 31088 | OMIM:613688 | Long QT syndrome 2 | | | | 3 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | ANK2 CL E G H | 287 | 493 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 539 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CACNA1C CL E G H | 775 | 1390 | OMIM:618447 | LONG QT SYNDROME 8; LQT8 | | | | 572 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CACNA1C CL E G H | 775 | 1390 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 572 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CALM1 CL E G H | 801 | 1442 | OMIM:616247 | Long QT syndrome 14 | | | | 18 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CALM1 CL E G H | 801 | 1442 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 18 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CALM2 CL E G H | 805 | 1445 | OMIM:616249 | Long QT syndrome 15 | . | | | 13 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CALM2 CL E G H | 805 | 1445 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 13 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CALM3 CL E G H | 808 | 1449 | OMIM:618782 | LONG QT SYNDROME 16; LQT16 | | | | 16 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CALM3 CL E G H | 808 | 1449 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 16 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | CAV3 CL E G H | 859 | 1529 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 148 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | FLNC CL E G H | 2318 | 3756 | OMIM:617047 | Cardiomyopathy, familial hypertrophic, 26 | | | | 197 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | HCN4 CL E G H | 10021 | 16882 | OMIM:163800 | Sick sinus syndrome 2 | | | | 185 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNA5 CL E G H | 3741 | 6224 | OMIM:612240 | Atrial fibrillation, familial, 7 | HP:0040283 - Occasional | | | 38 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNE1 CL E G H | 3753 | 6240 | ORPHA:90647 | Jervell and Lange-Nielsen syndrome | HP:0040281 - Very frequent | | | 148 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNE1 CL E G H | 3753 | 6240 | OMIM:613695 | Long QT syndrome 5 | | | | 148 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNE1 CL E G H | 3753 | 6240 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 148 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNE2 CL E G H | 9992 | 6242 | OMIM:613693 | Long QT syndrome 6 | | | | 43 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNE2 CL E G H | 9992 | 6242 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 43 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNH2 CL E G H | 3757 | 6251 | OMIM:613688 | Long QT syndrome 2 | | | | 901 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNH2 CL E G H | 3757 | 6251 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 901 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNJ2 CL E G H | 3759 | 6263 | OMIM:170390 | Andersen cardiodysrhythmic periodic paralysis | | | | 193 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNJ2 CL E G H | 3759 | 6263 | ORPHA:37553 | Andersen-Tawil syndrome | HP:0040283 - Occasional | | | 193 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNJ5 CL E G H | 3762 | 6266 | ORPHA:37553 | Andersen-Tawil syndrome | HP:0040283 - Occasional | | | 128 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNJ5 CL E G H | 3762 | 6266 | OMIM:613485 | Long QT syndrome 13 | | | | 128 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNJ5 CL E G H | 3762 | 6266 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 128 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:607554 | Atrial fibrillation, familial, 3 | | | | 730 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNQ1 CL E G H | 3784 | 6294 | ORPHA:90647 | Jervell and Lange-Nielsen syndrome | HP:0040281 - Very frequent | | | 730 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:220400 | Jervell and lange-nielsen syndrome 1 | | | | 730 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:192500 | LONG QT SYNDROME 1; LQT1 | | | | 730 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | KCNQ1 CL E G H | 3784 | 6294 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 730 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | MECP2 CL E G H | 4204 | 6990 | OMIM:312750 | Rett syndrome | . | | | 950 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | NOS1AP CL E G H | 9722 | 16859 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 4 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SCN10A CL E G H | 6336 | 10582 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 146 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SCN4B CL E G H | 6330 | 10592 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 110 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:603830 | Long QT syndrome 3 | | | | 1134 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SCN5A CL E G H | 6331 | 10593 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 1134 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SNTA1 CL E G H | 6640 | 11167 | OMIM:612955 | Long QT syndrome 12 | | | | 118 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SNTA1 CL E G H | 6640 | 11167 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 118 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | SVIL CL E G H | 6840 | 11480 | OMIM:619040 | MYOFIBRILLAR MYOPATHY 10; MFM10 | | | | 1 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | TANGO2 CL E G H | 128989 | 25439 | OMIM:616878 | Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration | | | | 12 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | TBX5 CL E G H | 6910 | 11604 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 123 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | TNNI3K CL E G H | 51086 | 19661 | OMIM:616117 | Cardiac conduction disease with or without dilated cardiomyopathy | . | | | 1 | | |
HP:0005184 | HP:0005184 | Prolonged QTc interval | 0 | TRDN CL E G H | 10345 | 12261 | ORPHA:101016 | Romano-Ward syndrome | HP:0040280 - Obligate | | | 145 | | |