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:0001695 | HP:0001695 | Cardiac arrest | 0 | ABCA12 CL E G H | 26154 | 14637 | ORPHA:457 | Harlequin ichthyosis | | | | 130 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ABCA3 CL E G H | 21 | 33 | ORPHA:70587 | Infant acute respiratory distress syndrome | HP:0040283 - Occasional | | | 147 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ABCC6 CL E G H | 368 | 57 | ORPHA:758 | Pseudoxanthoma elasticum | | | | 415 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ABCC9 CL E G H | 10060 | 60 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 254 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ABCG5 CL E G H | 64240 | 13886 | ORPHA:391665 | Homozygous familial hypercholesterolemia | | | | 67 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ABCG8 CL E G H | 64241 | 13887 | ORPHA:391665 | Homozygous familial hypercholesterolemia | | | | 76 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ACAD9 CL E G H | 28976 | 21497 | ORPHA:99901 | Acyl-CoA dehydrogenase 9 deficiency | | | | 98 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ACADVL CL E G H | 37 | 92 | OMIM:201475 | Very long-chain acyl-CoA dehydrogenase deficiency | | | | 200 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ACTC1 CL E G H | 70 | 143 | OMIM:612098 | Cardiomyopathy, familial hypertrophic, 11 | | | | 208 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ACTN2 CL E G H | 88 | 164 | OMIM:612158 | Cardiomyopathy, dilated, 1aa, with or without left ventricular noncompaction | HP:0040283 - Occasional | | | 307 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | AKAP9 CL E G H | 10142 | 379 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 289 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | AKAP9 CL E G H | 10142 | 379 | ORPHA:101016 | Romano-Ward syndrome | | | | 289 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | AKT1 CL E G H | 207 | 391 | ORPHA:744 | Proteus syndrome | | | | 54 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ALG10B CL E G H | 144245 | 31088 | OMIM:613688 | Long QT syndrome 2 | | | | 3 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ALPK3 CL E G H | 57538 | 17574 | OMIM:618052 | Cardiomyopathy, familial hypertrophic 27 | | | | 89 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ANK2 CL E G H | 287 | 493 | OMIM:600919 | Cardiac arrhythmia, ankyrin-b-related | | | | 539 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ANK2 CL E G H | 287 | 493 | ORPHA:101016 | Romano-Ward syndrome | | | | 539 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | APOB CL E G H | 338 | 603 | ORPHA:391665 | Homozygous familial hypercholesterolemia | | | | 356 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | BAZ1B CL E G H | 9031 | 961 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | BCL7B CL E G H | 9275 | 1005 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | BUD23 CL E G H | 114049 | 16405 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNA1C CL E G H | 775 | 1390 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 572 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNA1C CL E G H | 775 | 1390 | OMIM:611875 | BRUGADA SYNDROME 3; BRGDA3 | | | | 572 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNA1C CL E G H | 775 | 1390 | OMIM:618447 | LONG QT SYNDROME 8; LQT8 | | | | 572 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNA1C CL E G H | 775 | 1390 | ORPHA:101016 | Romano-Ward syndrome | | | | 572 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNA2D1 CL E G H | 781 | 1399 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 59 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNA2D1 CL E G H | 781 | 1399 | ORPHA:51083 | Familial short QT syndrome | | | | 59 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CACNB2 CL E G H | 783 | 1402 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 206 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM1 CL E G H | 801 | 1442 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 18 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM1 CL E G H | 801 | 1442 | OMIM:616247 | Long QT syndrome 14 | | | | 18 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM1 CL E G H | 801 | 1442 | ORPHA:101016 | Romano-Ward syndrome | | | | 18 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM1 CL E G H | 801 | 1442 | OMIM:614916 | Ventricular tachycardia, catecholaminergic polymorphic, 4 | . | | | 18 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM2 CL E G H | 805 | 1445 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 13 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM2 CL E G H | 805 | 1445 | OMIM:616249 | Long QT syndrome 15 | HP:0040283 - Occasional | | | 13 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM2 CL E G H | 805 | 1445 | ORPHA:101016 | Romano-Ward syndrome | | | | 13 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM3 CL E G H | 808 | 1449 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 16 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CALM3 CL E G H | 808 | 1449 | ORPHA:101016 | Romano-Ward syndrome | | | | 16 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CASQ2 CL E G H | 845 | 1513 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 129 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CASQ2 CL E G H | 845 | 1513 | OMIM:604772 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 | | | | 129 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CAV3 CL E G H | 859 | 1529 | OMIM:611818 | Long QT syndrome 9 | HP:0040283 - Occasional | | | 148 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CAV3 CL E G H | 859 | 1529 | ORPHA:101016 | Romano-Ward syndrome | | | | 148 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CLCF1 CL E G H | 23529 | 17412 | ORPHA:1545 | Crisponi syndrome | | | | 6 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CLIP2 CL E G H | 7461 | 2586 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CPT1A CL E G H | 1374 | 2328 | ORPHA:156 | Carnitine palmitoyl transferase 1A deficiency | | | | 99 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CRLF1 CL E G H | 9244 | 2364 | ORPHA:1545 | Crisponi syndrome | | | | 24 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | CSRP3 CL E G H | 8048 | 2472 | OMIM:612124 | Cardiomyopathy, familial hypertrophic, 12 | | | | 104 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DES CL E G H | 1674 | 2770 | ORPHA:98909 | Desminopathy | | | | 263 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DNAJC19 CL E G H | 131118 | 30528 | OMIM:610198 | 3-@methylglutaconic aciduria, type V | | | | 25 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DNAJC30 CL E G H | 84277 | 16410 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DPP6 CL E G H | 1804 | 3010 | OMIM:612956 | VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2; VF2 | | | | 18 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DSC2 CL E G H | 1824 | 3036 | OMIM:610476 | Arrhythmogenic right ventricular dysplasia, familial, 11 | | | | 268 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DSG2 CL E G H | 1829 | 3049 | OMIM:610193 | Arrhythmogenic right ventricular dysplasia, familial, 10 | | | | 358 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DSP CL E G H | 1832 | 3052 | OMIM:607450 | Arrhythmogenic right ventricular dysplasia, familial, 8 | | | | 747 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | DTNA CL E G H | 1837 | 3057 | OMIM:604169 | Left ventricular noncompaction 1 | | | | 163 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | EIF4H CL E G H | 7458 | 12741 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ELN CL E G H | 2006 | 3327 | ORPHA:904 | Williams syndrome | | | | 172 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | EMD CL E G H | 2010 | 3331 | OMIM:310300 | Emery-Dreifuss muscular dystrophy 1, X-linked | | | | 107 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | EMD CL E G H | 2010 | 3331 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | | | | 107 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:758 | Pseudoxanthoma elasticum | | | | 151 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | EYA4 CL E G H | 2070 | 3522 | OMIM:605362 | Cardiomyopathy, dilated, 1J | | | | 111 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | FHL1 CL E G H | 2273 | 3702 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | | | | 68 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | FHOD3 CL E G H | 80206 | 26178 | OMIM:619402 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 28; CMH28 | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | FKBP6 CL E G H | 8468 | 3722 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | FLNC CL E G H | 2318 | 3756 | OMIM:617047 | Cardiomyopathy, familial hypertrophic, 26 | | | | 197 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GBA1 CL E G H | 2629 | 4177 | ORPHA:77260 | Gaucher disease type 2 | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GNAI2 CL E G H | 2771 | 4385 | OMIM:192605 | Ventricular tachycardia, familial | | | | 4 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GPD1L CL E G H | 23171 | 28956 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 97 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GPD1L CL E G H | 23171 | 28956 | OMIM:611777 | BRUGADA SYNDROME 2; BRGDA2 | | | | 97 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GTF2I CL E G H | 2969 | 4659 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GTF2IRD1 CL E G H | 9569 | 4661 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | GTF2IRD2 CL E G H | 84163 | 30775 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | HCN4 CL E G H | 10021 | 16882 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 185 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | HCN4 CL E G H | 10021 | 16882 | OMIM:163800 | Sick sinus syndrome 2 | HP:0040283 - Occasional | | | 185 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | HLA-B CL E G H | 3106 | 4932 | ORPHA:397 | Giant cell arteritis | | | | 4 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | HLA-B CL E G H | 3106 | 4932 | ORPHA:36426 | Stevens-Johnson syndrome | | | | 4 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | HLA-DRB1 CL E G H | 3123 | 4948 | ORPHA:397 | Giant cell arteritis | | | | 2 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | HMGCL CL E G H | 3155 | 5005 | ORPHA:20 | 3-hydroxy-3-methylglutaric aciduria | HP:0040284 - Very rare | | | 35 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | IKZF1 CL E G H | 10320 | 13176 | ORPHA:36426 | Stevens-Johnson syndrome | | | | 8 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | IPO8 CL E G H | 10526 | 9853 | ORPHA:60030 | Loeys-Dietz syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | JUP CL E G H | 3728 | 6207 | OMIM:601214 | Naxos disease | | | | 222 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | JUP CL E G H | 3728 | 6207 | ORPHA:34217 | Naxos disease | | | | 222 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCND3 CL E G H | 3752 | 6239 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 35 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE1 CL E G H | 3753 | 6240 | OMIM:612347 | Jervell and lange-nielsen syndrome 2 | | | | 148 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE1 CL E G H | 3753 | 6240 | OMIM:613695 | Long QT syndrome 5 | | | | 148 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE1 CL E G H | 3753 | 6240 | ORPHA:101016 | Romano-Ward syndrome | | | | 148 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE2 CL E G H | 9992 | 6242 | OMIM:613693 | Long QT syndrome 6 | | | | 43 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE2 CL E G H | 9992 | 6242 | ORPHA:101016 | Romano-Ward syndrome | | | | 43 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE3 CL E G H | 10008 | 6243 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 73 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE3 CL E G H | 10008 | 6243 | OMIM:613119 | BRUGADA SYNDROME 6; BRGDA6 | | | | 73 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNE5 CL E G H | 23630 | 6241 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 5 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNH2 CL E G H | 3757 | 6251 | ORPHA:51083 | Familial short QT syndrome | | | | 901 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNH2 CL E G H | 3757 | 6251 | OMIM:613688 | Long QT syndrome 2 | | | | 901 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNH2 CL E G H | 3757 | 6251 | ORPHA:101016 | Romano-Ward syndrome | | | | 901 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNH2 CL E G H | 3757 | 6251 | OMIM:609620 | SHORT QT SYNDROME 1; SQT1 | | | | 901 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNJ2 CL E G H | 3759 | 6263 | ORPHA:51083 | Familial short QT syndrome | | | | 193 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNJ5 CL E G H | 3762 | 6266 | OMIM:613485 | Long QT syndrome 13 | . | | | 128 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNJ5 CL E G H | 3762 | 6266 | ORPHA:101016 | Romano-Ward syndrome | | | | 128 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNJ8 CL E G H | 3764 | 6269 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 23 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNQ1 CL E G H | 3784 | 6294 | ORPHA:51083 | Familial short QT syndrome | | | | 730 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:220400 | Jervell and lange-nielsen syndrome 1 | | | | 730 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:192500 | LONG QT SYNDROME 1; LQT1 | | | | 730 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNQ1 CL E G H | 3784 | 6294 | ORPHA:101016 | Romano-Ward syndrome | | | | 730 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:609621 | Short QT syndrome 2 | | | | 730 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LDB3 CL E G H | 11155 | 15710 | OMIM:601493 | Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction | | | | 286 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LDLR CL E G H | 3949 | 6547 | ORPHA:391665 | Homozygous familial hypercholesterolemia | | | | 2157 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LDLRAP1 CL E G H | 26119 | 18640 | ORPHA:391665 | Homozygous familial hypercholesterolemia | | | | 73 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LEMD2 CL E G H | 221496 | 21244 | OMIM:212500 | CATARACT 46, JUVENILE-ONSET; CTRCT46 | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LIMK1 CL E G H | 3984 | 6613 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 645 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:98855 | Autosomal recessive Emery-Dreifuss muscular dystrophy | | | | 645 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LMNA CL E G H | 4000 | 6636 | OMIM:115200 | Cardiomyopathy, dilated, 1A | | | | 645 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LMNA CL E G H | 4000 | 6636 | OMIM:181350 | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | | | | 645 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | | | | 645 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | LRP6 CL E G H | 4040 | 6698 | OMIM:610947 | Coronary artery disease, autosomal dominant 2 | | | | 26 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | METTL27 CL E G H | 155368 | 19068 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MLXIPL CL E G H | 51085 | 12744 | ORPHA:904 | Williams syndrome | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MRPL12 CL E G H | 6182 | 10378 | OMIM:618951 | COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45; COXPD45 | | | | 11 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MYBPC3 CL E G H | 4607 | 7551 | OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | . | | | 1143 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MYH7 CL E G H | 4625 | 7577 | OMIM:613426 | Cardiomyopathy, dilated, 1S | | | | 1269 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MYH7 CL E G H | 4625 | 7577 | ORPHA:1880 | Ebstein malformation of the tricuspid valve | | | | 1269 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MYL2 CL E G H | 4633 | 7583 | OMIM:608758 | Cardiomyopathy, familial hypertrophic, 10 | | | | 131 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MYL3 CL E G H | 4634 | 7584 | OMIM:608751 | Cardiomyopathy, familial hypertrophic, 8 | . | | | 95 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | MYOZ2 CL E G H | 51778 | 1330 | OMIM:613838 | Cardiomyopathy, familial hypertrophic, 16 | | | | 81 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | NCF1 CL E G H | 653361 | 7660 | ORPHA:904 | Williams syndrome | | | | 13 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | NDUFB11 CL E G H | 54539 | 20372 | OMIM:300952 | Linear skin defects with multiple congenital anomalies 3 | . | | | 3 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | NOS1AP CL E G H | 9722 | 16859 | ORPHA:101016 | Romano-Ward syndrome | | | | 4 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | NUP155 CL E G H | 9631 | 8063 | OMIM:615770 | Atrial fibrillation, familial, 15 | | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | P4HA2 CL E G H | 8974 | 8547 | ORPHA:397 | Giant cell arteritis | | | | 3 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PCSK9 CL E G H | 255738 | 20001 | ORPHA:391665 | Homozygous familial hypercholesterolemia | | | | 178 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PGM1 CL E G H | 5236 | 8905 | OMIM:614921 | Congenital disorder of glycosylation, type It | | | | 58 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PKP2 CL E G H | 5318 | 9024 | OMIM:609040 | Arrhythmogenic right ventricular dysplasia, familial, 9 | | | | 406 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PKP2 CL E G H | 5318 | 9024 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 406 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PPA2 CL E G H | 27068 | 28883 | OMIM:617222 | Sudden cardiac failure, infantile | | | | 8 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PRKAG2 CL E G H | 51422 | 9386 | OMIM:600858 | Cardiomyopathy, familial hypertrophic, 6 | | | | 235 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PRKAG2 CL E G H | 51422 | 9386 | OMIM:194200 | WOLFF-PARKINSON-WHITE SYNDROME | | | | 235 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PTEN CL E G H | 5728 | 9588 | ORPHA:744 | Proteus syndrome | | | | 948 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | PTPN22 CL E G H | 26191 | 9652 | ORPHA:397 | Giant cell arteritis | | | | 3 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RAB3GAP2 CL E G H | 25782 | 17168 | OMIM:212720 | Martsolf syndrome 1 | | | | 135 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RANGRF CL E G H | 29098 | 17679 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 22 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RBM20 CL E G H | 282996 | 27424 | OMIM:613172 | Cardiomyopathy, dilated, 1dd | | | | 363 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RFC2 CL E G H | 5982 | 9970 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RYR2 CL E G H | 6262 | 10484 | OMIM:115000 | CARDIAC ARRHYTHMIA | | | | 1103 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RYR2 CL E G H | 6262 | 10484 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 1103 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | RYR2 CL E G H | 6262 | 10484 | OMIM:604772 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 | | | | 1103 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN10A CL E G H | 6336 | 10582 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 146 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN10A CL E G H | 6336 | 10582 | ORPHA:101016 | Romano-Ward syndrome | | | | 146 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN1B CL E G H | 6324 | 10586 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 126 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN2B CL E G H | 6327 | 10589 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 21 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN3B CL E G H | 55800 | 20665 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 122 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN4B CL E G H | 6330 | 10592 | OMIM:611819 | Long QT syndrome 10 | | | | 110 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN4B CL E G H | 6330 | 10592 | ORPHA:101016 | Romano-Ward syndrome | | | | 110 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN5A CL E G H | 6331 | 10593 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 1134 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:601144 | BRUGADA SYNDROME 1; BRGDA1 | | | | 1134 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:603830 | Long QT syndrome 3 | | | | 1134 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN5A CL E G H | 6331 | 10593 | OMIM:113900 | Progressive familial heart block, type IA | | | | 1134 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCN5A CL E G H | 6331 | 10593 | ORPHA:101016 | Romano-Ward syndrome | | | | 1134 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCNN1A CL E G H | 6337 | 10599 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 67 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SCO2 CL E G H | 9997 | 10604 | OMIM:604377 | Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 | | | | 40 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SEMA3A CL E G H | 10371 | 10723 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 14 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SFTPB CL E G H | 6439 | 10801 | ORPHA:70587 | Infant acute respiratory distress syndrome | HP:0040283 - Occasional | | | 51 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SFTPC CL E G H | 6440 | 10802 | ORPHA:70587 | Infant acute respiratory distress syndrome | HP:0040283 - Occasional | | | 33 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SGCD CL E G H | 6444 | 10807 | OMIM:606685 | CARDIOMYOPATHY, DILATED, 1L; CMD1L | | | | 223 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SLC19A2 CL E G H | 10560 | 10938 | ORPHA:49827 | Thiamine-responsive megaloblastic anemia syndrome | HP:0040283 - Occasional | | | 55 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SLC25A20 CL E G H | 788 | 1421 | OMIM:212138 | Carnitine-acylcarnitine translocase deficiency | | | | 40 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SLC2A10 CL E G H | 81031 | 13444 | ORPHA:3342 | Arterial tortuosity syndrome | HP:0040283 - Occasional | | | 178 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SLC4A3 CL E G H | 6508 | 11029 | ORPHA:51083 | Familial short QT syndrome | | | | 7 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SLMAP CL E G H | 7871 | 16643 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 18 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SNTA1 CL E G H | 6640 | 11167 | ORPHA:101016 | Romano-Ward syndrome | | | | 118 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | STX1A CL E G H | 6804 | 11433 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SYNE1 CL E G H | 23345 | 17089 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 1129 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | SYNE2 CL E G H | 23224 | 17084 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 508 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TANGO2 CL E G H | 128989 | 25439 | OMIM:616878 | Metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration | . | | | 12 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TBL2 CL E G H | 26608 | 11586 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TBX5 CL E G H | 6910 | 11604 | ORPHA:101016 | Romano-Ward syndrome | | | | 123 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TECRL CL E G H | 253017 | 27365 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 4 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TECRL CL E G H | 253017 | 27365 | OMIM:614021 | Ventricular tachycardia, catecholaminergic polymorphic, 3 | | | | 4 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TGFB3 CL E G H | 7043 | 11769 | OMIM:107970 | Arrhythmogenic right ventricular dysplasia, familial, 1 | | | | 85 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TGFBR1 CL E G H | 7046 | 11772 | ORPHA:60030 | Loeys-Dietz syndrome | HP:0040283 - Occasional | | | 239 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TGFBR2 CL E G H | 7048 | 11773 | ORPHA:60030 | Loeys-Dietz syndrome | HP:0040283 - Occasional | | | 253 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TMEM270 CL E G H | 135886 | 23018 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TMEM43 CL E G H | 79188 | 28472 | OMIM:604400 | Arrhythmogenic right ventricular dysplasia, familial, 5 | | | | 171 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TMEM43 CL E G H | 79188 | 28472 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | | | | 171 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TNNC1 CL E G H | 7134 | 11943 | OMIM:611879 | CARDIOMYOPATHY, DILATED, 1Z; CMD1Z | | | | 73 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TNNI3 CL E G H | 7137 | 11947 | OMIM:115210 | CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1 | | | | 180 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TNNI3K CL E G H | 51086 | 19661 | OMIM:616117 | Cardiac conduction disease with or without dilated cardiomyopathy | HP:0040284 - Very rare | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TNNT2 CL E G H | 7139 | 11949 | OMIM:601494 | Cardiomyopathy, dilated, 1D | | | | 248 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TOR1A CL E G H | 1861 | 3098 | OMIM:618947 | ARTHROGRYPOSIS MULTIPLEX CONGENITA 5; AMC5 | | | | 47 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TPM1 CL E G H | 7168 | 12010 | OMIM:115196 | Cardiomyopathy, familial hypertrophic, 3 | | | | 230 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TRDN CL E G H | 10345 | 12261 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | | | | 145 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TRDN CL E G H | 10345 | 12261 | ORPHA:101016 | Romano-Ward syndrome | | | | 145 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TRDN CL E G H | 10345 | 12261 | OMIM:604772 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 | | | | 145 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TRDN CL E G H | 10345 | 12261 | OMIM:615441 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH OR WITHOUT MUSCLE WEAKNESS; CPVT5 | | | | 145 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TRPM4 CL E G H | 54795 | 17993 | ORPHA:130 | Brugada syndrome | HP:0040282 - Frequent | | | 124 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TSPYL1 CL E G H | 7259 | 12382 | ORPHA:168593 | Sudden infant death-dysgenesis of the testes syndrome | HP:0040281 - Very frequent | | | 1 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | TTC26 CL E G H | 79989 | 21882 | OMIM:619534 | BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME; BRENS | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | VPS37D CL E G H | 155382 | 18287 | ORPHA:904 | Williams syndrome | | | | | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | WAS CL E G H | 7454 | 12731 | ORPHA:906 | Wiskott-Aldrich syndrome | | | | 65 | | |
HP:0001695 | HP:0001695 | Cardiac arrest | 0 | WIPF1 CL E G H | 7456 | 12736 | ORPHA:906 | Wiskott-Aldrich syndrome | | | | 6 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ABCA12 CL E G H | 26154 | 14637 | ORPHA:457 | Harlequin ichthyosis | HP:0040283 - Occasional | | | 130 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ABCC6 CL E G H | 368 | 57 | ORPHA:758 | Pseudoxanthoma elasticum | HP:0040283 - Occasional | | | 415 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ABCG5 CL E G H | 64240 | 13886 | ORPHA:391665 | Homozygous familial hypercholesterolemia | HP:0040282 - Frequent | | | 67 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ABCG8 CL E G H | 64241 | 13887 | ORPHA:391665 | Homozygous familial hypercholesterolemia | HP:0040282 - Frequent | | | 76 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ACAD9 CL E G H | 28976 | 21497 | ORPHA:99901 | Acyl-CoA dehydrogenase 9 deficiency | HP:0040283 - Occasional | | | 98 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ACADVL CL E G H | 37 | 92 | OMIM:201475 | Very long-chain acyl-CoA dehydrogenase deficiency | . | | | 200 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | AKAP9 CL E G H | 10142 | 379 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 289 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | AKT1 CL E G H | 207 | 391 | ORPHA:744 | Proteus syndrome | HP:0040283 - Occasional | | | 54 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ALG10B CL E G H | 144245 | 31088 | OMIM:613688 | Long QT syndrome 2 | . | | | 3 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ANK2 CL E G H | 287 | 493 | OMIM:600919 | Cardiac arrhythmia, ankyrin-b-related | . | | | 539 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ANK2 CL E G H | 287 | 493 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 539 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | APOB CL E G H | 338 | 603 | ORPHA:391665 | Homozygous familial hypercholesterolemia | HP:0040282 - Frequent | | | 356 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | BAZ1B CL E G H | 9031 | 961 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | BCL7B CL E G H | 9275 | 1005 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | BUD23 CL E G H | 114049 | 16405 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CACNA1C CL E G H | 775 | 1390 | OMIM:611875 | BRUGADA SYNDROME 3; BRGDA3 | | | | 572 | | |
HP:0001695 | HP:0031628 | Aborted sudden cardiac death | 1 | CACNA1C CL E G H | 775 | 1390 | OMIM:618447 | LONG QT SYNDROME 8; LQT8 | | | | 572 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CACNA1C CL E G H | 775 | 1390 | OMIM:618447 | LONG QT SYNDROME 8; LQT8 | | | | 572 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CACNA1C CL E G H | 775 | 1390 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 572 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CACNA2D1 CL E G H | 781 | 1399 | ORPHA:51083 | Familial short QT syndrome | HP:0040283 - Occasional | | | 59 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM1 CL E G H | 801 | 1442 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 18 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM1 CL E G H | 801 | 1442 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 18 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM1 CL E G H | 801 | 1442 | OMIM:614916 | Ventricular tachycardia, catecholaminergic polymorphic, 4 | | | | 18 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM2 CL E G H | 805 | 1445 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 13 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM2 CL E G H | 805 | 1445 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 13 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM3 CL E G H | 808 | 1449 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 16 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CALM3 CL E G H | 808 | 1449 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 16 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CASQ2 CL E G H | 845 | 1513 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 129 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CASQ2 CL E G H | 845 | 1513 | OMIM:604772 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 | | | | 129 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CAV3 CL E G H | 859 | 1529 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 148 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CLCF1 CL E G H | 23529 | 17412 | ORPHA:1545 | Crisponi syndrome | HP:0040281 - Very frequent | | | 6 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CLIP2 CL E G H | 7461 | 2586 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CPT1A CL E G H | 1374 | 2328 | ORPHA:156 | Carnitine palmitoyl transferase 1A deficiency | HP:0040283 - Occasional | | | 99 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CRLF1 CL E G H | 9244 | 2364 | ORPHA:1545 | Crisponi syndrome | HP:0040281 - Very frequent | | | 24 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | CSRP3 CL E G H | 8048 | 2472 | OMIM:612124 | Cardiomyopathy, familial hypertrophic, 12 | . | | | 104 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DES CL E G H | 1674 | 2770 | ORPHA:98909 | Desminopathy | HP:0040283 - Occasional | | | 263 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DNAJC19 CL E G H | 131118 | 30528 | OMIM:610198 | 3-@methylglutaconic aciduria, type V | . | | | 25 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DNAJC30 CL E G H | 84277 | 16410 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DPP6 CL E G H | 1804 | 3010 | OMIM:612956 | VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2; VF2 | | | | 18 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DSC2 CL E G H | 1824 | 3036 | OMIM:610476 | Arrhythmogenic right ventricular dysplasia, familial, 11 | . | | | 268 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DSG2 CL E G H | 1829 | 3049 | OMIM:610193 | Arrhythmogenic right ventricular dysplasia, familial, 10 | . | | | 358 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DSP CL E G H | 1832 | 3052 | OMIM:607450 | Arrhythmogenic right ventricular dysplasia, familial, 8 | . | | | 747 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | DTNA CL E G H | 1837 | 3057 | OMIM:604169 | Left ventricular noncompaction 1 | . | | | 163 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | EIF4H CL E G H | 7458 | 12741 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ELN CL E G H | 2006 | 3327 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 172 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | EMD CL E G H | 2010 | 3331 | OMIM:310300 | Emery-Dreifuss muscular dystrophy 1, X-linked | . | | | 107 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | EMD CL E G H | 2010 | 3331 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | HP:0040284 - Very rare | | | 107 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | ENPP1 CL E G H | 5167 | 3356 | ORPHA:758 | Pseudoxanthoma elasticum | HP:0040283 - Occasional | | | 151 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | EYA4 CL E G H | 2070 | 3522 | OMIM:605362 | Cardiomyopathy, dilated, 1J | | | | 111 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | FHL1 CL E G H | 2273 | 3702 | ORPHA:98863 | X-linked Emery-Dreifuss muscular dystrophy | HP:0040284 - Very rare | | | 68 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | FHOD3 CL E G H | 80206 | 26178 | OMIM:619402 | CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 28; CMH28 | | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | FKBP6 CL E G H | 8468 | 3722 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | FLNC CL E G H | 2318 | 3756 | OMIM:617047 | Cardiomyopathy, familial hypertrophic, 26 | | | | 197 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | GNAI2 CL E G H | 2771 | 4385 | OMIM:192605 | Ventricular tachycardia, familial | . | | | 4 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | GPD1L CL E G H | 23171 | 28956 | OMIM:611777 | BRUGADA SYNDROME 2; BRGDA2 | | | | 97 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | GTF2I CL E G H | 2969 | 4659 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | GTF2IRD1 CL E G H | 9569 | 4661 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | GTF2IRD2 CL E G H | 84163 | 30775 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | HLA-B CL E G H | 3106 | 4932 | ORPHA:397 | Giant cell arteritis | HP:0040283 - Occasional | | | 4 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | HLA-B CL E G H | 3106 | 4932 | ORPHA:36426 | Stevens-Johnson syndrome | HP:0040283 - Occasional | | | 4 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | HLA-DRB1 CL E G H | 3123 | 4948 | ORPHA:397 | Giant cell arteritis | HP:0040283 - Occasional | | | 2 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | IKZF1 CL E G H | 10320 | 13176 | ORPHA:36426 | Stevens-Johnson syndrome | HP:0040283 - Occasional | | | 8 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | JUP CL E G H | 3728 | 6207 | ORPHA:34217 | Naxos disease | HP:0040283 - Occasional | | | 222 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | JUP CL E G H | 3728 | 6207 | OMIM:601214 | Naxos disease | | | | 222 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNE1 CL E G H | 3753 | 6240 | OMIM:612347 | Jervell and lange-nielsen syndrome 2 | . | | | 148 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNE1 CL E G H | 3753 | 6240 | OMIM:613695 | Long QT syndrome 5 | . | | | 148 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNE1 CL E G H | 3753 | 6240 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 148 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNE2 CL E G H | 9992 | 6242 | OMIM:613693 | Long QT syndrome 6 | . | | | 43 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNE2 CL E G H | 9992 | 6242 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 43 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNH2 CL E G H | 3757 | 6251 | ORPHA:51083 | Familial short QT syndrome | HP:0040283 - Occasional | | | 901 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNH2 CL E G H | 3757 | 6251 | OMIM:613688 | Long QT syndrome 2 | . | | | 901 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNH2 CL E G H | 3757 | 6251 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 901 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNH2 CL E G H | 3757 | 6251 | OMIM:609620 | SHORT QT SYNDROME 1; SQT1 | | | | 901 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNJ2 CL E G H | 3759 | 6263 | ORPHA:51083 | Familial short QT syndrome | HP:0040283 - Occasional | | | 193 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNJ5 CL E G H | 3762 | 6266 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 128 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNQ1 CL E G H | 3784 | 6294 | ORPHA:51083 | Familial short QT syndrome | HP:0040283 - Occasional | | | 730 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:220400 | Jervell and lange-nielsen syndrome 1 | . | | | 730 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:192500 | LONG QT SYNDROME 1; LQT1 | | | | 730 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNQ1 CL E G H | 3784 | 6294 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 730 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | KCNQ1 CL E G H | 3784 | 6294 | OMIM:609621 | Short QT syndrome 2 | | | | 730 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LDB3 CL E G H | 11155 | 15710 | OMIM:601493 | Cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction | HP:0040283 - Occasional | | | 286 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LDLR CL E G H | 3949 | 6547 | ORPHA:391665 | Homozygous familial hypercholesterolemia | HP:0040282 - Frequent | | | 2157 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LDLRAP1 CL E G H | 26119 | 18640 | ORPHA:391665 | Homozygous familial hypercholesterolemia | HP:0040282 - Frequent | | | 73 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LEMD2 CL E G H | 221496 | 21244 | OMIM:212500 | CATARACT 46, JUVENILE-ONSET; CTRCT46 | | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LIMK1 CL E G H | 3984 | 6613 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LMNA CL E G H | 4000 | 6636 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040284 - Very rare | | | 645 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LMNA CL E G H | 4000 | 6636 | ORPHA:98855 | Autosomal recessive Emery-Dreifuss muscular dystrophy | HP:0040282 - Frequent | | | 645 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LMNA CL E G H | 4000 | 6636 | OMIM:115200 | Cardiomyopathy, dilated, 1A | | | | 645 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LMNA CL E G H | 4000 | 6636 | OMIM:181350 | Emery-Dreifuss muscular dystrophy 2, autosomal dominant | . | | | 645 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LMNA CL E G H | 4000 | 6636 | ORPHA:300751 | Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | HP:0040282 - Frequent | | | 645 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | LRP6 CL E G H | 4040 | 6698 | OMIM:610947 | Coronary artery disease, autosomal dominant 2 | . | | | 26 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | METTL27 CL E G H | 155368 | 19068 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MLXIPL CL E G H | 51085 | 12744 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MYBPC3 CL E G H | 4607 | 7551 | OMIM:115197 | Cardiomyopathy, familial hypertrophic, 4 | | | | 1143 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MYH7 CL E G H | 4625 | 7577 | OMIM:613426 | Cardiomyopathy, dilated, 1S | | | | 1269 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MYH7 CL E G H | 4625 | 7577 | ORPHA:1880 | Ebstein malformation of the tricuspid valve | HP:0040283 - Occasional | | | 1269 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MYL2 CL E G H | 4633 | 7583 | OMIM:608758 | Cardiomyopathy, familial hypertrophic, 10 | HP:0040283 - Occasional | | | 131 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MYL3 CL E G H | 4634 | 7584 | OMIM:608751 | Cardiomyopathy, familial hypertrophic, 8 | . | | | 95 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | MYOZ2 CL E G H | 51778 | 1330 | OMIM:613838 | Cardiomyopathy, familial hypertrophic, 16 | | | | 81 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | NCF1 CL E G H | 653361 | 7660 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | 13 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | NOS1AP CL E G H | 9722 | 16859 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 4 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | NUP155 CL E G H | 9631 | 8063 | OMIM:615770 | Atrial fibrillation, familial, 15 | | | | 1 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | P4HA2 CL E G H | 8974 | 8547 | ORPHA:397 | Giant cell arteritis | HP:0040283 - Occasional | | | 3 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PCSK9 CL E G H | 255738 | 20001 | ORPHA:391665 | Homozygous familial hypercholesterolemia | HP:0040282 - Frequent | | | 178 | | |
HP:0001695 | HP:0031628 | Aborted sudden cardiac death | 1 | PGM1 CL E G H | 5236 | 8905 | OMIM:614921 | Congenital disorder of glycosylation, type It | | | | 58 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PGM1 CL E G H | 5236 | 8905 | OMIM:614921 | Congenital disorder of glycosylation, type It | | | | 58 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PKP2 CL E G H | 5318 | 9024 | OMIM:609040 | Arrhythmogenic right ventricular dysplasia, familial, 9 | . | | | 406 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PPA2 CL E G H | 27068 | 28883 | OMIM:617222 | Sudden cardiac failure, infantile | | | | 8 | | |
HP:0001695 | HP:0031628 | Aborted sudden cardiac death | 1 | PRKAG2 CL E G H | 51422 | 9386 | OMIM:600858 | Cardiomyopathy, familial hypertrophic, 6 | | | | 235 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PRKAG2 CL E G H | 51422 | 9386 | OMIM:194200 | WOLFF-PARKINSON-WHITE SYNDROME | | | | 235 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PTEN CL E G H | 5728 | 9588 | ORPHA:744 | Proteus syndrome | HP:0040283 - Occasional | | | 948 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | PTPN22 CL E G H | 26191 | 9652 | ORPHA:397 | Giant cell arteritis | HP:0040283 - Occasional | | | 3 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | RBM20 CL E G H | 282996 | 27424 | OMIM:613172 | Cardiomyopathy, dilated, 1dd | . | | | 363 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | RFC2 CL E G H | 5982 | 9970 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | RYR2 CL E G H | 6262 | 10484 | OMIM:115000 | CARDIAC ARRHYTHMIA | | | | 1103 | | |
HP:0001695 | HP:0031628 | Aborted sudden cardiac death | 1 | RYR2 CL E G H | 6262 | 10484 | OMIM:115000 | CARDIAC ARRHYTHMIA | | | | 1103 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | RYR2 CL E G H | 6262 | 10484 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 1103 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | RYR2 CL E G H | 6262 | 10484 | OMIM:604772 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 | | | | 1103 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN10A CL E G H | 6336 | 10582 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 146 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN4B CL E G H | 6330 | 10592 | OMIM:611819 | Long QT syndrome 10 | | | | 110 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN4B CL E G H | 6330 | 10592 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 110 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN5A CL E G H | 6331 | 10593 | OMIM:601144 | BRUGADA SYNDROME 1; BRGDA1 | | | | 1134 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN5A CL E G H | 6331 | 10593 | OMIM:603830 | Long QT syndrome 3 | . | | | 1134 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN5A CL E G H | 6331 | 10593 | OMIM:113900 | Progressive familial heart block, type IA | . | | | 1134 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SCN5A CL E G H | 6331 | 10593 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 1134 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SGCD CL E G H | 6444 | 10807 | OMIM:606685 | CARDIOMYOPATHY, DILATED, 1L; CMD1L | | | | 223 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SLC4A3 CL E G H | 6508 | 11029 | ORPHA:51083 | Familial short QT syndrome | HP:0040283 - Occasional | | | 7 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SNTA1 CL E G H | 6640 | 11167 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 118 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | STX1A CL E G H | 6804 | 11433 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SYNE1 CL E G H | 23345 | 17089 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040284 - Very rare | | | 1129 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | SYNE2 CL E G H | 23224 | 17084 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040284 - Very rare | | | 508 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TBL2 CL E G H | 26608 | 11586 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TBX5 CL E G H | 6910 | 11604 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 123 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TECRL CL E G H | 253017 | 27365 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 4 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TGFB3 CL E G H | 7043 | 11769 | OMIM:107970 | Arrhythmogenic right ventricular dysplasia, familial, 1 | . | | | 85 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TMEM270 CL E G H | 135886 | 23018 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TMEM43 CL E G H | 79188 | 28472 | OMIM:604400 | Arrhythmogenic right ventricular dysplasia, familial, 5 | | | | 171 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TMEM43 CL E G H | 79188 | 28472 | ORPHA:98853 | Autosomal dominant Emery-Dreifuss muscular dystrophy | HP:0040284 - Very rare | | | 171 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TNNC1 CL E G H | 7134 | 11943 | OMIM:611879 | CARDIOMYOPATHY, DILATED, 1Z; CMD1Z | | | | 73 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TNNI3 CL E G H | 7137 | 11947 | OMIM:115210 | CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1; RCM1 | | | | 180 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TNNT2 CL E G H | 7139 | 11949 | OMIM:601494 | Cardiomyopathy, dilated, 1D | | | | 248 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TPM1 CL E G H | 7168 | 12010 | OMIM:115196 | Cardiomyopathy, familial hypertrophic, 3 | | | | 230 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TRDN CL E G H | 10345 | 12261 | ORPHA:3286 | Catecholaminergic polymorphic ventricular tachycardia | HP:0040283 - Occasional | | | 145 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TRDN CL E G H | 10345 | 12261 | ORPHA:101016 | Romano-Ward syndrome | HP:0040283 - Occasional | | | 145 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | TRDN CL E G H | 10345 | 12261 | OMIM:604772 | VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1, WITH OR WITHOUT ATRIAL DYSFUNCTION AND/OR DILATED CARDIOMYOPATHY; CPVT1 | | | | 145 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | VPS37D CL E G H | 155382 | 18287 | ORPHA:904 | Williams syndrome | HP:0040283 - Occasional | | | | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | WAS CL E G H | 7454 | 12731 | ORPHA:906 | Wiskott-Aldrich syndrome | HP:0040283 - Occasional | | | 65 | | |
HP:0001695 | HP:0001645 | Sudden cardiac death | 1 | WIPF1 CL E G H | 7456 | 12736 | ORPHA:906 | Wiskott-Aldrich syndrome | HP:0040283 - Occasional | | | 6 | | |