Ventricular hypertrophy

Symptom Information:

Symptom ID: HPO:0001714
Synonyms:
Ventricular hypertrophy [OMIM:Ventricular hypertrophy]
Ventricular hypertrophy (1/4 patients) [OMIM:Ventricular hypertrophy (1/4 patients)]
Ventricular hypertrophy [MedDRA:10047295]
Quality:
Cross references:
OMIM: "Ventricular hypertrophy" [OMIM:Ventricular hypertrophy]
OMIM: "Ventricular hypertrophy (1/4 patients)" [OMIM:Ventricular hypertrophy (1/4 patients)]
Is a (Direct Parents):
MedDRA Myocardial disorders NEC
HPO         Abnormality of cardiac ventricle
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)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Myocardial disorders NEC(MedDRA:10028590)
          Ventricular hypertrophy(HPO:0001714)
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
Arterial tortuosity syndrome (Orphanet:3342)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
CARDIOAUDITORY SYNDROME OF SANCHEZ CASCOS (OMIM:212100)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cardiomyopathy, familial hypertrophic, 15 (OMIM:613255)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Carnitine-acylcarnitine translocase deficiency (Orphanet:159)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Loeffler endocarditis (Orphanet:75566)
Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type (Orphanet:217026)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mucopolysaccharidosis type 2 (Orphanet:580)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
PULMONIC STENOSIS AND DEAFNESS (OMIM:178651)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Steinert myotonic dystrophy (Orphanet:273)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)