Right ventricular hypertrophy

Symptom Information:

Symptom ID: HPO:0001667
Synonyms:
Right ventricular hypertrophy [OMIM:Right ventricular hypertrophy]
Right ventricular hypertrophy (1 patient) [OMIM:Right ventricular hypertrophy (1 patient)]
Right ventricular hypertrophy (report in 2 sibs) [OMIM:Right ventricular hypertrophy (report in 2 sibs)]
Right ventricular hypertrophy (reported in 2 sibs) [OMIM:Right ventricular hypertrophy (reported in 2 sibs)]
Right ventricular hypertrophy [MedDRA:10050326]
Quality:
Cross references:
OMIM: "Right ventricular hypertrophy" [OMIM:Right ventricular hypertrophy]
OMIM: "Right ventricular hypertrophy (1 patient)" [OMIM:Right ventricular hypertrophy (1 patient)]
OMIM: "Right ventricular hypertrophy (report in 2 sibs)" [OMIM:Right ventricular hypertrophy (report in 2 sibs)]
OMIM: "Right ventricular hypertrophy (reported in 2 sibs)" [OMIM:Right ventricular hypertrophy (reported in 2 sibs)]
Is a (Direct Parents):
HPO         Abnormality of the right ventricle
HPO         Ventricular hypertrophy
MedDRA Myocardial disorders NEC
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 cardiac ventricle(HPO:0001713)
                   Abnormality of the right ventricle(HPO:0001707)
                      Right ventricular hypertrophy(HPO:0001667)
                   Ventricular hypertrophy(HPO:0001714)
                      Right ventricular hypertrophy(HPO:0001667)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Myocardial disorders NEC(MedDRA:10028590)
          Right ventricular hypertrophy(HPO:0001667)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 (OMIM:613404)
ATTRV122I amyloidosis (Orphanet:85451)
Alström syndrome (Orphanet:64)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Cryptogenic organizing pneumonia (Orphanet:1302)
Heritable pulmonary arterial hypertension (Orphanet:275777)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Hypoplastic left heart syndrome 1 (OMIM:241550)
Idiopathic and/or familial pulmonary arterial hypertension (Orphanet:422)
Idiopathic pulmonary arterial hypertension (Orphanet:275766)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Noonan syndrome with multiple lentigines (Orphanet:500)
PULMONARY HYPERTENSION, PRIMARY, 1 (OMIM:178600)
PULMONARY HYPERTENSION, PRIMARY, AUTOSOMAL RECESSIVE (OMIM:265400)
Pulmonary capillary hemangiomatosis (Orphanet:199241)
Pulmonary venoocclusive disease (Orphanet:31837)
ROWLEY-ROSENBERG SYNDROME (OMIM:268500)
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 (OMIM:208085)