Biventricular hypertrophy

Symptom Information:

Symptom ID: HPO:0200128
Synonyms:
Biventricular hypertrophy [OMIM:Biventricular hypertrophy]
Biventricular hypertrophy (in one patient) [OMIM:Biventricular hypertrophy (in one patient)]
Quality:
Cross references:
OMIM: "Biventricular hypertrophy" [OMIM:Biventricular hypertrophy]
OMIM: "Biventricular hypertrophy (in one patient)" [OMIM:Biventricular hypertrophy (in one patient)]
Is a (Direct Parents):
HPO         Left ventricular hypertrophy
HPO         Right ventricular hypertrophy
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)
                         Biventricular hypertrophy(HPO:0200128)
                      Left ventricular hypertrophy(HPO:0001712)
                         Biventricular hypertrophy(HPO:0200128)
                   Abnormality of the right ventricle(HPO:0001707)
                      Right ventricular hypertrophy(HPO:0001667)
                         Biventricular hypertrophy(HPO:0200128)
                   Abnormality of the left ventricle(HPO:0001711)
                      Left ventricular hypertrophy(HPO:0001712)
                         Biventricular hypertrophy(HPO:0200128)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

3-methylglutaconic aciduria type 4 (Orphanet:67048)
ATTRV122I amyloidosis (Orphanet:85451)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, familial hypertrophic, 13 (OMIM:613243)
Fabry disease (Orphanet:324)
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease (Orphanet:439854)
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency (Orphanet:289527)
Left ventricular noncompaction (Orphanet:54260)
Nephronophthisis 9 (OMIM:613824)
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL (OMIM:261740)