Cor pulmonale

Symptom Information:

Symptom ID: HPO:0001648
Synonyms:
Cor pulmonale [OMIM:Cor pulmonale]
Cor pulmonale (reported in 1 family) [OMIM:Cor pulmonale (reported in 1 family)]
Cor pulmonale [MedDRA:10010968]
Quality:
Cross references:
OMIM: "Cor pulmonale" [OMIM:Cor pulmonale]
OMIM: "Cor pulmonale (reported in 1 family)" [OMIM:Cor pulmonale (reported in 1 family)]
Is a (Direct Parents):
HPO         Abnormality of the right ventricle
MedDRA Right ventricular failure
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)
                      Cor pulmonale(HPO:0001648)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Congestive heart failure(HPO:0001635)
       Right ventricular failure(HPO:0001708)
          Cor pulmonale(HPO:0001648)
Vascular disorders(MedDRA:10047065)
    Decreased and nonspecific blood pressure disorders and shock(MedDRA:10011954)
       Circulatory collapse and shock(MedDRA:10009193)
          Congestive heart failure(HPO:0001635)
             Right ventricular failure(HPO:0001708)
                Cor pulmonale(HPO:0001648)
Database Frequency: 16 / 7739
Resource:

All diseases associated with this symptom:

AGAMMAGLOBULINEMIA, X-LINKED (OMIM:300755)
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
Cryptogenic organizing pneumonia (Orphanet:1302)
Cystic fibrosis (Orphanet:586)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Desquamative interstitial pneumonia (Orphanet:98852)
Frontometaphyseal dysplasia (Orphanet:1826)
German syndrome (Orphanet:2077)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Idiopathic pulmonary fibrosis (Orphanet:2032)
Isolated Pierre Robin syndrome (Orphanet:718)
Lymphoid interstitial pneumonia (Orphanet:79128)
ROWLEY-ROSENBERG SYNDROME (OMIM:268500)
Scheie syndrome (Orphanet:93474)