Left bundle branch block

Symptom Information:

Symptom ID: HPO:0011713
Synonyms:
Left bundle branch block [OMIM:Left bundle branch block]
Left bundle branch block (in some patients) [OMIM:Left bundle branch block (in some patients)]
Quality:
Cross references:
OMIM: "Left bundle branch block" [OMIM:Left bundle branch block]
OMIM: "Left bundle branch block (in some patients)" [OMIM:Left bundle branch block (in some patients)]
Is a (Direct Parents):
HPO         Bundle branch block
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)
                Abnormal atrioventricular conduction(HPO:0005150)
                   Bundle branch block(HPO:0011710)
                      Left bundle branch block(HPO:0011713)
MedDRA:
Database Frequency: 30 / 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, 13 (OMIM:615616)
Arrhythmogenic right ventricular dysplasia, familial, 2 (OMIM:600996)
Arrhythmogenic right ventricular dysplasia, familial, 4 (OMIM:602087)
Arrhythmogenic right ventricular dysplasia, familial, 6 (OMIM:604401)
Arrhythmogenic right ventricular dysplasia, familial, 8 (OMIM:607450)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1E (OMIM:601154)
Cardiomyopathy, dilated, 1EE (OMIM:613252)
Cardiomyopathy, dilated, 1HH (OMIM:613881)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiomyopathy, dilated, 1S (OMIM:613426)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Cardiomyopathy, familial hypertrophic, 16 (OMIM:613838)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial hypertrophic, 6 (OMIM:600858)
Desminopathy (Orphanet:98909)
Familial isolated arrhythmogenic right ventricular dysplasia (Orphanet:217656)
Familial progressive cardiac conduction defect (Orphanet:871)
Hypertrophic cardiomyopathy due to intensive athletic training (Orphanet:217601)
Incessant infant ventricular tachycardia (Orphanet:45453)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Peripartum cardiomyopathy (Orphanet:563)
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome (Orphanet:228012)
Senile systemic amyloidosis (Orphanet:330001)
Uhl anomaly (Orphanet:3403)
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 (OMIM:107970)