Bundle branch block

Symptom Information:

Symptom ID: HPO:0011710
Synonyms:
Bundle branch block (disorder) [Orphanet:35060]
Bundle-Branch Block [Orphanet:35060]
Bundle branch block [OMIM:Bundle branch block]
Cardiac conduction defect/sinoauricular/heart/auriculoventricular/branch block [Orphanet:35060]
Bundle branch block [Orphanet:35060]
Bundle branch block [MedDRA:10006578]
Block bundle branch [MedDRA:10006578]
Bundle branch block NOS [MedDRA:10006578]
Bundle branch block, other and unspecified [MedDRA:10006578]
Bundle branch block, unspecified [MedDRA:10006578]
Heart block bundle branch [MedDRA:10006578]
Incomplete bundle branch block [MedDRA:10006578]
Complete bundle branch block [MedDRA:10006578]
Sinoatrial block [MedDRA:10040736]
Sinoatrial nodal block [Orphanet:35060]
Sinoatrial block (disorder) [Orphanet:35060]
Sinoatrial Block [Orphanet:35060]
Nodal block [Orphanet:35060]
Sinoatrial block [OMIM:Sinoatrial block]
Quality:
Cross references:
Orphanet:35060 "Cardiac conduction defect/sinoauricular/heart/auriculoventricular/branch block" [Orphanet:35060]
OMIM: "Bundle branch block" [OMIM:Bundle branch block]
OMIM: "Sinoatrial block" [OMIM:Sinoatrial block]
UMLS:C0006384 "Bundle-Branch Block" [Orphanet:35060]
UMLS:C0037188 "Sinoatrial Block" [Orphanet:35060]
UMLS:C0857153 "Nodal block" [Orphanet:35060]
Is a (Direct Parents):
Orphanet Atrioventricular block
MedDRA Cardiac conduction disorders
Orphanet Abnormality of cardiovascular system physiology
HPO         Abnormal atrioventricular conduction
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)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Arrhythmia(HPO:0011675)
       Cardiac conduction disorders(MedDRA:10000032)
          Bundle branch block(HPO:0011710)
Investigations(MedDRA:10022891)
    Cardiac and vascular investigations (excl enzyme tests)(MedDRA:10007512)
       ECG investigations(MedDRA:10053104)
          Arrhythmia(HPO:0011675)
             Cardiac conduction disorders(MedDRA:10000032)
                Bundle branch block(HPO:0011710)
       Heart rate and pulse investigations(MedDRA:10053103)
          Arrhythmia(HPO:0011675)
             Cardiac conduction disorders(MedDRA:10000032)
                Bundle branch block(HPO:0011710)
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

BRUGADA SYNDROME 5 (OMIM:612838)
Cardiomyopathy, dilated, 1HH (OMIM:613881)
Cardiomyopathy, dilated, 1V (OMIM:613697)
Cardiomyopathy, familial hypertrophic, 14 (OMIM:613251)
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation (Orphanet:300751)
Familial progressive cardiac conduction defect (Orphanet:871)
Glycogen storage disease due to acid maltase deficiency (Orphanet:365)
Kearns-Sayre syndrome (Orphanet:480)
LEOPARD SYNDROME 1 (OMIM:151100)
MELAS (Orphanet:550)
MENTAL RETARDATION, KERATOCONUS, FEBRILE SEIZURES, AND SINOATRIALBLOCK (OMIM:609438)
Maternally-inherited diabetes and deafness (Orphanet:225)
Noonan syndrome with multiple lentigines (Orphanet:500)
Steinert myotonic dystrophy (Orphanet:273)