Right bundle branch block

Symptom Information:

Symptom ID: HPO:0011712
Synonyms:
Right bundle branch block [OMIM:Right bundle branch block]
Right bundle branch block (1 patient) [OMIM:Right bundle branch block (1 patient)]
Bundle branch block right [MedDRA:10006582]
Quality:
Cross references:
OMIM: "Right bundle branch block" [OMIM:Right bundle branch block]
OMIM: "Right bundle branch block (1 patient)" [OMIM:Right bundle branch block (1 patient)]
Is a (Direct Parents):
HPO         Bundle branch block
MedDRA Cardiac conduction disorders
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)
                      Right bundle branch block(HPO:0011712)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Cardiac conduction disorders(MedDRA:10000032)
          Right bundle branch block(HPO:0011712)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Cardiac conduction disorders(MedDRA:10000032)
                Right bundle branch block(HPO:0011712)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Cardiac conduction disorders(MedDRA:10000032)
                Right bundle branch block(HPO:0011712)
Database Frequency: 34 / 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, 13 (OMIM:615616)
Atrial fibrillation, familial, 7 (OMIM:612240)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
Autosomal recessive limb-girdle muscular dystrophy type 2N (Orphanet:206559)
BRUGADA SYNDROME 2 (OMIM:611777)
BUNDLE BRANCH BLOCK, FAMILIAL ISOLATED COMPLETE RIGHT (OMIM:113950)
Brugada syndrome (Orphanet:130)
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, with woolly hair, keratoderma, and toothagenesis (OMIM:615821)
Cardiomyopathy, familial hypertrophic, 1 (OMIM:192600)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Desminopathy (Orphanet:98909)
Ebstein malformation (Orphanet:1880)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial progressive cardiac conduction defect (Orphanet:871)
Familial short QT syndrome (Orphanet:51083)
Glycogen storage disease due to glycogenin deficiency (Orphanet:263297)
Idiopathic giant cell myocarditis (Orphanet:329874)
Incessant infant ventricular tachycardia (Orphanet:45453)
Left vetricular noncompaction 7 (OMIM:615092)
MERRF (Orphanet:551)
Naxos disease (Orphanet:34217)
Nestor-Guillermo progeria syndrome (Orphanet:280576)
PROGRESSIVE FAMILIAL HEART BLOCK, TYPE IA (OMIM:113900)
Senile systemic amyloidosis (Orphanet:330001)
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 (OMIM:107970)