Palpitations
Symptom Information:
| Symptom ID: | HPO:0001962 | ||||
| Synonyms: |
|
||||
| Quality: | |||||
| Cross references: |
|
||||
| Is a (Direct Parents): |
|
||||
| Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormality of cardiovascular system physiology(HPO:0011025) Arrhythmia(HPO:0011675) Palpitations(HPO:0001962) MedDRA: Cardiac disorders(MedDRA:10007541) Cardiac disorder signs and symptoms(MedDRA:10007539) Cardiac signs and symptoms NEC(MedDRA:10007609) Palpitations(HPO:0001962) |
||||
| Database Frequency: | 62 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| Arrhythmogenic right ventricular dysplasia, familial, 10 | (OMIM:610193) |
| Arrhythmogenic right ventricular dysplasia, familial, 11 | (OMIM:610476) |
| Arrhythmogenic right ventricular dysplasia, familial, 5 | (OMIM:604400) |
| Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
| Atrial fibrillation, familial, 10 | (OMIM:614022) |
| Atrial fibrillation, familial, 3 | (OMIM:607554) |
| Atrial fibrillation, familial, 7 | (OMIM:612240) |
| Atrial standstill | (Orphanet:1344) |
| Atrial standstill 2 | (OMIM:615745) |
| Atrial tachyarrhythmia with short PR interval | (Orphanet:844) |
| Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
| Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
| Autosomal recessive limb girdle muscular dystrophy type 2A | (Orphanet:267) |
| Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
| Brugada syndrome | (Orphanet:130) |
| Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
| Cardiomyopathy, dilated, 1E | (OMIM:601154) |
| Cardiomyopathy, dilated, 1Y | (OMIM:611878) |
| Cardiomyopathy, familial hypertrophic, 1 | (OMIM:192600) |
| Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
| Cardiomyopathy, familial hypertrophic, 16 | (OMIM:613838) |
| Cardiomyopathy, familial hypertrophic, 17 | (OMIM:613873) |
| Cardiomyopathy, familial hypertrophic, 18 | (OMIM:613874) |
| Catecholaminergic polymorphic ventricular tachycardia | (Orphanet:3286) |
| Fabry disease | (Orphanet:324) |
| Familial atrial fibrillation | (Orphanet:334) |
| Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
| Familial isolated dilated cardiomyopathy | (Orphanet:154) |
| Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
| Familial isolated restrictive cardiomyopathy | (Orphanet:75249) |
| Familial short QT syndrome | (Orphanet:51083) |
| Familial sick sinus syndrome | (Orphanet:166282) |
| Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
| Hemochromatosis, type 2A | (OMIM:602390) |
| Hereditary myopathy with lactic acidosis due to ISCU deficiency | (Orphanet:43115) |
| Hereditary pheochromocytoma-paraganglioma | (Orphanet:29072) |
| Hereditary pheochromocytoma-paraganglioma | (Orphanet:29072) |
| Idiopathic giant cell myocarditis | (Orphanet:329874) |
| Limited systemic sclerosis | (Orphanet:220407) |
| MERRF | (Orphanet:551) |
| Multifocal atrial tachycardia | (Orphanet:3282) |
| Naxos disease | (Orphanet:34217) |
| PARAGANGLIOMAS 1 | (OMIM:168000) |
| PARAGANGLIOMAS 1 | (OMIM:168000) |
| PARAGANGLIOMAS 3 | (OMIM:605373) |
| PARAGANGLIOMAS 3 | (OMIM:605373) |
| PARAGANGLIOMAS 4 | (OMIM:115310) |
| Peripartum cardiomyopathy | (Orphanet:563) |
| Primary erythermalgia | (Orphanet:90026) |
| Proximal myotonic myopathy | (Orphanet:606) |
| SHORT QT SYNDROME 3 | (OMIM:609622) |
| Sarcoidosis | (Orphanet:797) |
| Senile systemic amyloidosis | (Orphanet:330001) |
| Sino-auricular heart block | (Orphanet:1260) |
| Sodium channelopathy-related small fiber neuropathy | (Orphanet:306577) |
| THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 | (OMIM:188580) |
| THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 | (OMIM:613239) |
| Tako-Tsubo cardiomyopathy | (Orphanet:66529) |
| Thyrotoxic periodic paralysis | (Orphanet:79102) |
| WOLFF-PARKINSON-WHITE SYNDROME | (OMIM:194200) |
| X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
| [DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |