Ventricular arrhythmia

Symptom Information:

Symptom ID: HPO:0004308
Synonyms:
Ventricular arrhythmias [HPO:0004308]
Ventricular arrhythmia [OMIM:Ventricular arrhythmia]
Ventricular arrhythmias [OMIM:Ventricular arrhythmias]
Ventricular arrhythmia (PVC, NSVT, and VT) [OMIM:Ventricular arrhythmia (PVC, NSVT, and VT)]
Ventricular arrhythmia (PVC, VT, and VF) [OMIM:Ventricular arrhythmia (PVC, VT, and VF)]
Ventricular arrhythmia (PVC, nonsustained VT, sustained VT) [OMIM:Ventricular arrhythmia (PVC, nonsustained VT, sustained VT)]
Ventricular arrhythmia (in some patients) [OMIM:Ventricular arrhythmia (in some patients)]
Ventricular arrhythmia (sustained VT) [OMIM:Ventricular arrhythmia (sustained VT)]
Ventricular arrhythmia [MedDRA:10047281]
Quality:
Cross references:
OMIM: "Ventricular arrhythmia" [OMIM:Ventricular arrhythmia]
OMIM: "Ventricular arrhythmias" [OMIM:Ventricular arrhythmias]
OMIM: "Ventricular arrhythmia (PVC, NSVT, and VT)" [OMIM:Ventricular arrhythmia (PVC, NSVT, and VT)]
OMIM: "Ventricular arrhythmia (PVC, VT, and VF)" [OMIM:Ventricular arrhythmia (PVC, VT, and VF)]
OMIM: "Ventricular arrhythmia (PVC, nonsustained VT, sustained VT)" [OMIM:Ventricular arrhythmia (PVC, nonsustained VT, sustained VT)]
OMIM: "Ventricular arrhythmia (in some patients)" [OMIM:Ventricular arrhythmia (in some patients)]
OMIM: "Ventricular arrhythmia (sustained VT)" [OMIM:Ventricular arrhythmia (sustained VT)]
Is a (Direct Parents):
HPO         Arrhythmia
MedDRA Ventricular arrhythmias and cardiac arrest
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)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Ventricular arrhythmia(HPO:0004308)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Ventricular arrhythmia(HPO:0004308)
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)