Ventricular arrhythmia
Symptom Information:
Symptom ID: | HPO:0004308 | |||||||||
Synonyms: |
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Cross references: |
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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) MedDRA: Cardiac disorders(MedDRA:10007541) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Ventricular arrhythmia(HPO:0004308) Investigations(MedDRA:10022891) Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512) ECG investigations(MedDRA:10053104) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Ventricular arrhythmia(HPO:0004308) Heart rate and pulse investigations(MedDRA:10053103) Arrhythmia(HPO:0011675) Ventricular arrhythmias and cardiac arrest(MedDRA:10047283) Ventricular arrhythmia(HPO:0004308) |
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Database Frequency: | 46 / 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, 12 | (OMIM:611528) |
Arrhythmogenic right ventricular dysplasia, familial, 2 | (OMIM:600996) |
Arrhythmogenic right ventricular dysplasia, familial, 3 | (OMIM:602086) |
Arrhythmogenic right ventricular dysplasia, familial, 4 | (OMIM:602087) |
Arrhythmogenic right ventricular dysplasia, familial, 8 | (OMIM:607450) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
BRUGADA SYNDROME 3 | (OMIM:611875) |
Barth syndrome | (Orphanet:111) |
Becker muscular dystrophy | (Orphanet:98895) |
Brugada syndrome | (Orphanet:130) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, dilated, 1B | (OMIM:600884) |
Cardiomyopathy, dilated, 1C | (OMIM:601493) |
Cardiomyopathy, dilated, 1P | (OMIM:609909) |
Cardiomyopathy, dilated, 1R | (OMIM:613424) |
Cardiomyopathy, dilated, 1S | (OMIM:613426) |
Cardiomyopathy, dilated, 1nn | (OMIM:615916) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Fabry disease | (Orphanet:324) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Familial isolated hypertrophic cardiomyopathy | (Orphanet:155) |
Familial long QT syndrome | (Orphanet:768) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Glycogen storage disease due to glycogenin deficiency | (Orphanet:263297) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Jervell and Lange-Nielsen syndrome | (Orphanet:90647) |
Kasabach-Merritt syndrome | (Orphanet:2330) |
Kearns-Sayre syndrome | (Orphanet:480) |
Left ventricular noncompaction | (Orphanet:54260) |
Left ventricular noncompaction 1 | (OMIM:604169) |
Loeffler endocarditis | (Orphanet:75566) |
Long QT syndrome 1 | (OMIM:192500) |
Long QT syndrome 10 | (OMIM:611819) |
Long QT syndrome 2 | (OMIM:613688) |
Long QT syndrome 3 | (OMIM:603830) |
Long QT syndrome 9 | (OMIM:611818) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Naxos disease | (Orphanet:34217) |
Peripartum cardiomyopathy | (Orphanet:563) |
Romano-Ward syndrome | (Orphanet:101016) |
Timothy syndrome | (Orphanet:65283) |
Torsade-de-pointes syndrome with short coupling interval | (Orphanet:51084) |
Uhl anomaly | (Orphanet:3403) |
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |