Bundle branch block
Symptom Information:
Symptom ID: | HPO:0011710 | |||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |