Ventricular tachycardia

Symptom Information:

Symptom ID: HPO:0004756
Synonyms:
Ventricular tachycardia [OMIM:Ventricular tachycardia]
Tachycardia, ventricular [OMIM:Tachycardia, ventricular]
Ventricular tachycardia (Vtach) [OMIM:Ventricular tachycardia (Vtach)]
Ventricular tachycardia (in some patients) [OMIM:Ventricular tachycardia (in some patients)]
Ventricular tachycardia [MedDRA:10047302]
Quality:
Cross references:
OMIM: "Ventricular tachycardia" [OMIM:Ventricular tachycardia]
OMIM: "Tachycardia, ventricular" [OMIM:Tachycardia, ventricular]
OMIM: "Ventricular tachycardia (Vtach)" [OMIM:Ventricular tachycardia (Vtach)]
OMIM: "Ventricular tachycardia (in some patients)" [OMIM:Ventricular tachycardia (in some patients)]
Is a (Direct Parents):
MedDRA Ventricular arrhythmias and cardiac arrest
HPO         Tachycardia
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)
                Tachycardia(HPO:0001649)
                   Ventricular tachycardia(HPO:0004756)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
          Ventricular tachycardia(HPO:0004756)
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 tachycardia(HPO:0004756)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Ventricular tachycardia(HPO:0004756)
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

AA amyloidosis (Orphanet:85445)
Arrhythmogenic right ventricular dysplasia, familial, 10 (OMIM:610193)
Arrhythmogenic right ventricular dysplasia, familial, 12 (OMIM:611528)
Arrhythmogenic right ventricular dysplasia, familial, 13 (OMIM:615616)
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, 5 (OMIM:604400)
Arrhythmogenic right ventricular dysplasia, familial, 6 (OMIM:604401)
Arrhythmogenic right ventricular dysplasia, familial, 8 (OMIM:607450)
Arrhythmogenic right ventricular dysplasia, familial, 9 (OMIM:609040)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
BRUGADA SYNDROME 8 (OMIM:613123)
Brugada syndrome (Orphanet:130)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1O (OMIM:608569)
Cardiomyopathy, dilated, 1P (OMIM:609909)
Cardiomyopathy, dilated, 1Y (OMIM:611878)
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Cardiomyopathy, familial hypertrophic, 10 (OMIM:608758)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Cardiomyopathy, familial hypertrophic, 16 (OMIM:613838)
Cardiomyopathy, familial hypertrophic, 17 (OMIM:613873)
Cardiomyopathy, familial hypertrophic, 4 (OMIM:115197)
Carnitine-acylcarnitine translocase deficiency (Orphanet:159)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
DK1-CDG (Orphanet:91131)
Desminopathy (Orphanet:98909)
Fabry disease (Orphanet:324)
Familial isolated arrhythmogenic right ventricular dysplasia (Orphanet:217656)
Familial long QT syndrome (Orphanet:768)
Familial short QT syndrome (Orphanet:51083)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Hemochromatosis, type 2A (OMIM:602390)
Histiocytoid cardiomyopathy (Orphanet:137675)
Idiopathic giant cell myocarditis (Orphanet:329874)
Incessant infant ventricular tachycardia (Orphanet:45453)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Left ventricular noncompaction (Orphanet:54260)
Long QT syndrome 1 (OMIM:192500)
Long QT syndrome 2 (OMIM:613688)
MERRF (Orphanet:551)
Naxos disease (Orphanet:34217)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Romano-Ward syndrome (Orphanet:101016)
Sarcoidosis (Orphanet:797)
Timothy syndrome (Orphanet:65283)
Torsade-de-pointes syndrome with short coupling interval (Orphanet:51084)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 2 (OMIM:611938)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 3 (OMIM:614021)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 4 (OMIM:614916)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 5, WITH ORWITHOUT MUSCLE WEAKNESS (OMIM:615441)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)