Right ventricular hypertrophy
Symptom Information:
Symptom ID: | HPO:0001667 | ||||||
Synonyms: |
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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 cardiac ventricle(HPO:0001713) Ventricular hypertrophy(HPO:0001714) Right ventricular hypertrophy(HPO:0001667) Abnormality of the right ventricle(HPO:0001707) 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) |
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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) |