Ventricular fibrillation

Symptom Information:

Symptom ID: HPO:0001663
Synonyms:
Ventricular fibrillation [OMIM:Ventricular fibrillation]
Ventricular fibrillation [MedDRA:10047290]
Quality:
Cross references:
OMIM: "Ventricular fibrillation" [OMIM:Ventricular fibrillation]
Is a (Direct Parents):
HPO         Ventricular 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)
                   Ventricular fibrillation(HPO:0001663)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
          Ventricular fibrillation(HPO:0001663)
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 fibrillation(HPO:0001663)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Ventricular arrhythmias and cardiac arrest(MedDRA:10047283)
                Ventricular fibrillation(HPO:0001663)
Database Frequency: 35 / 7739
Resource:

All diseases associated with this symptom:

Arrhythmogenic right ventricular dysplasia, familial, 11 (OMIM:610476)
Arrhythmogenic right ventricular dysplasia, familial, 8 (OMIM:607450)
Atrial fibrillation, familial, 3 (OMIM:607554)
BRUGADA SYNDROME 2 (OMIM:611777)
BRUGADA SYNDROME 5 (OMIM:612838)
BRUGADA SYNDROME 6 (OMIM:613119)
Brugada syndrome (Orphanet:130)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1EE (OMIM:613252)
Cardiomyopathy, dilated, 1P (OMIM:609909)
Cardiomyopathy, familial hypertrophic, 13 (OMIM:613243)
Catecholaminergic polymorphic ventricular tachycardia (Orphanet:3286)
DK1-CDG (Orphanet:91131)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Familial long QT syndrome (Orphanet:768)
Familial short QT syndrome (Orphanet:51083)
Hemochromatosis, type 2A (OMIM:602390)
Histiocytoid cardiomyopathy (Orphanet:137675)
Idiopathic giant cell myocarditis (Orphanet:329874)
Idiopathic ventricular fibrillation, not Brugada type (Orphanet:228140)
Jervell and Lange-Nielsen syndrome (Orphanet:90647)
Long QT syndrome 1 (OMIM:192500)
Long QT syndrome 2 (OMIM:613688)
Long QT syndrome 3 (OMIM:603830)
Long QT syndrome 5 (OMIM:613695)
Long QT syndrome 6 (OMIM:613693)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Romano-Ward syndrome (Orphanet:101016)
Tako-Tsubo cardiomyopathy (Orphanet:66529)
Torsade-de-pointes syndrome with short coupling interval (Orphanet:51084)
Uhl anomaly (Orphanet:3403)
Ventricular fibrillation, paroxysmal familial, 1 (OMIM:603829)
Ventricular fibrillation, paroxysmal familial, 2 (OMIM:612956)
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 (OMIM:107970)