Right ventricular cardiomyopathy

Symptom Information:

Symptom ID: HPO:0011663
Synonyms:
CARDIOMYOPATHY, ESP. RIGHT VENTRICULAR [HPO:0011663]
CARDIOMYOPATHY, RIGHT VENTRICULAR [HPO:0011663]
Cardiomyopathy, right ventricular [OMIM:Cardiomyopathy, right ventricular]
Cardiomyopathy, esp. right ventricular [OMIM:Cardiomyopathy, esp. right ventricular]
Quality:
Cross references:
OMIM: "Cardiomyopathy, right ventricular" [OMIM:Cardiomyopathy, right ventricular]
OMIM: "Cardiomyopathy, esp. right ventricular" [OMIM:Cardiomyopathy, esp. right ventricular]
Is a (Direct Parents):
HPO         Cardiomyopathy
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:
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)