Ventricular extrasystoles
Symptom Information:
Symptom ID: | HPO:0006682 | ||||||
Synonyms: |
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Is a (Direct Parents): |
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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) Ventricular arrhythmia(HPO:0004308) Ventricular extrasystoles(HPO:0006682) MedDRA: Cardiac disorders(MedDRA:10007541) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Ventricular extrasystoles(HPO:0006682) Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) Heart rate and pulse investigations(MedDRA:10053103) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Ventricular extrasystoles(HPO:0006682) ECG investigations(MedDRA:10053104) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Ventricular extrasystoles(HPO:0006682) |
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Database Frequency: | 25 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Arrhythmogenic right ventricular dysplasia, familial, 10 | (OMIM:610193) |
Arrhythmogenic right ventricular dysplasia, familial, 4 | (OMIM:602087) |
Arrhythmogenic right ventricular dysplasia, familial, 5 | (OMIM:604400) |
Arrhythmogenic right ventricular dysplasia, familial, 6 | (OMIM:604401) |
Arrhythmogenic right ventricular dysplasia, familial, 8 | (OMIM:607450) |
Atrial fibrillation, familial, 7 | (OMIM:612240) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, dilated, 1DD | (OMIM:613172) |
Cardiomyopathy, dilated, 1E | (OMIM:601154) |
Cardiomyopathy, dilated, 1HH | (OMIM:613881) |
Cardiomyopathy, dilated, 1P | (OMIM:609909) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Catecholaminergic polymorphic ventricular tachycardia | (Orphanet:3286) |
EXTRASYSTOLES, MULTIFORM VENTRICULAR, WITH SHORT STATURE, HYPERPIGMENTATIONAND MICROCEPHALY | (OMIM:133750) |
Familial atrial fibrillation | (Orphanet:334) |
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | (Orphanet:436242) |
Familial short QT syndrome | (Orphanet:51083) |
Idiopathic ventricular fibrillation, not Brugada type | (Orphanet:228140) |
MERRF | (Orphanet:551) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Naxos disease | (Orphanet:34217) |
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome | (Orphanet:276432) |
Torsade-de-pointes syndrome with short coupling interval | (Orphanet:51084) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |