Right ventricular cardiomyopathy
Symptom Information:
Symptom ID: | HPO:0011663 | ||||
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) Abnormal heart morphology(HPO:0001627) obsolete Malformation of the heart and great vessels(HPO:0002564) Abnormality of the myocardium(HPO:0001637) Cardiomyopathy(HPO:0001638) Right ventricular cardiomyopathy(HPO:0011663) MedDRA: |
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Database Frequency: | 17 / 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, 3 | (OMIM:602086) |
Arrhythmogenic right ventricular dysplasia, familial, 4 | (OMIM:602087) |
Arrhythmogenic right ventricular dysplasia, familial, 5 | (OMIM:604400) |
Arrhythmogenic right ventricular dysplasia, familial, 6 | (OMIM:604401) |
Arrhythmogenic right ventricular dysplasia, familial, 8 | (OMIM:607450) |
Arrhythmogenic right ventricular dysplasia, familial, 9 | (OMIM:609040) |
Desminopathy | (Orphanet:98909) |
Familial cutaneous collagenoma | (Orphanet:53296) |
Familial isolated arrhythmogenic right ventricular dysplasia | (Orphanet:217656) |
MERRF | (Orphanet:551) |
Uhl anomaly | (Orphanet:3403) |
[DEL] Arrhythmogenic right ventricular dysplasia, familial, 1 | (OMIM:107970) |