Left bundle branch block
Symptom Information:
Symptom ID: | HPO:0011713 | ||
Synonyms: |
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Quality: | |||
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) Left bundle branch block(HPO:0011713) MedDRA: |
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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) |