Paroxysmal ventricular tachycardia
Symptom Information:
Symptom ID: | HPO:0004751 | ||
Synonyms: |
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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) Tachycardia(HPO:0001649) Ventricular tachycardia(HPO:0004756) Paroxysmal ventricular tachycardia(HPO:0004751) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Familial short QT syndrome | (Orphanet:51083) |
Hemochromatosis, type 2A | (OMIM:602390) |
Idiopathic ventricular fibrillation, not Brugada type | (Orphanet:228140) |
VENTRICULAR TACHYCARDIA, FAMILIAL | (OMIM:192605) |