Prolonged QRS complex
Symptom Information:
Symptom ID: | HPO:0006677 | ||
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) Abnormal EKG(HPO:0003115) Prolonged QRS complex(HPO:0006677) MedDRA: |
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Database Frequency: | 16 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Arrhythmogenic right ventricular dysplasia, familial, 10 | (OMIM:610193) |
Arrhythmogenic right ventricular dysplasia, familial, 12 | (OMIM:611528) |
Arrhythmogenic right ventricular dysplasia, familial, 2 | (OMIM:600996) |
Arrhythmogenic right ventricular dysplasia, familial, 3 | (OMIM:602086) |
Arrhythmogenic right ventricular dysplasia, familial, 4 | (OMIM:602087) |
Arrhythmogenic right ventricular dysplasia, familial, 5 | (OMIM:604400) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
Atrial fibrillation, familial, 10 | (OMIM:614022) |
Atrial fibrillation, familial, 3 | (OMIM:607554) |
Brugada syndrome | (Orphanet:130) |
Cardiomyopathy, familial hypertrophic, 6 | (OMIM:600858) |
Familial progressive cardiac conduction defect | (Orphanet:871) |
Incessant infant ventricular tachycardia | (Orphanet:45453) |
Naxos disease | (Orphanet:34217) |
Noonan syndrome | (Orphanet:648) |
WOLFF-PARKINSON-WHITE SYNDROME | (OMIM:194200) |