Left ventricular hypertrophy

Symptom Information:

Symptom ID: HPO:0001712
Synonyms:
Left ventricular wall hypertrophy [HPO:0001712]
Left ventricular hypertrophy [OMIM:Left ventricular hypertrophy]
Left ventricular wall hypertrophy [OMIM:Left ventricular wall hypertrophy]
Left ventricular hypertrophy (1 patient) [OMIM:Left ventricular hypertrophy (1 patient)]
Left ventricular hypertrophy (in some patients) [OMIM:Left ventricular hypertrophy (in some patients)]
Left ventricular hypertrophy [MedDRA:10049773]
Left ventricular enlargement [OMIM, cm]
Quality:
Cross references:
OMIM: "Left ventricular hypertrophy" [OMIM:Left ventricular hypertrophy]
OMIM: "Left ventricular wall hypertrophy" [OMIM:Left ventricular wall hypertrophy]
OMIM: "Left ventricular hypertrophy (1 patient)" [OMIM:Left ventricular hypertrophy (1 patient)]
OMIM: "Left ventricular hypertrophy (in some patients)" [OMIM:Left ventricular hypertrophy (in some patients)]
Is a (Direct Parents):
MedDRA Myocardial disorders NEC
HPO         Ventricular hypertrophy
HPO         Abnormality of the left 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)
                      Left ventricular hypertrophy(HPO:0001712)
                   Abnormality of the left ventricle(HPO:0001711)
                      Left ventricular hypertrophy(HPO:0001712)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Myocardial disorders NEC(MedDRA:10028590)
          Left ventricular hypertrophy(HPO:0001712)
Database Frequency: 76 / 7739
Resource:

All diseases associated with this symptom:

Acromegaly (Orphanet:963)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Alström syndrome (Orphanet:64)
Aneurysm - osteoarthritis syndrome (Orphanet:284984)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Atrial fibrillation, familial, 10 (OMIM:614022)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
Bardet-Biedl syndrome (Orphanet:110)
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 (OMIM:617047)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
Cardiomyopathy, dilated, 1C (OMIM:601493)
Cardiomyopathy, dilated, 1D (OMIM:601494)
Cardiomyopathy, dilated, 1DD (OMIM:613172)
Cardiomyopathy, dilated, 1GG (OMIM:613642)
Cardiomyopathy, dilated, 1HH (OMIM:613881)
Cardiomyopathy, dilated, 1KK (OMIM:615248)
Cardiomyopathy, dilated, 1M (OMIM:607482)
Cardiomyopathy, dilated, 1P (OMIM:609909)
Cardiomyopathy, dilated, 1R (OMIM:613424)
Cardiomyopathy, familial hypertrophic, 1 (OMIM:192600)
Cardiomyopathy, familial hypertrophic, 11 (OMIM:612098)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Cardiomyopathy, familial hypertrophic, 14 (OMIM:613251)
Cardiomyopathy, familial hypertrophic, 16 (OMIM:613838)
Cardiomyopathy, familial hypertrophic, 17 (OMIM:613873)
Cardiomyopathy, familial hypertrophic, 18 (OMIM:613874)
Cardiomyopathy, familial hypertrophic, 19 (OMIM:613875)
Cardiomyopathy, familial hypertrophic, 2 (OMIM:115195)
Cardiomyopathy, familial hypertrophic, 20 (OMIM:613876)
Cardiomyopathy, familial hypertrophic, 21 (OMIM:614676)
Cardiomyopathy, familial hypertrophic, 3 (OMIM:115196)
Cardiomyopathy, familial hypertrophic, 4 (OMIM:115197)
Cardiomyopathy, familial hypertrophic, 7 (OMIM:613690)
Cardiomyopathy, familial hypertrophic, 8 (OMIM:608751)
Cardiomyopathy, familial hypertrophic, 9 (OMIM:613765)
Cardiomyopathy, familial restrictive, 3 (OMIM:612422)
Cardiomyopathy, hypertrophic, 25 (OMIM:607487)
Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (Orphanet:293955)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome (Orphanet:319678)
Fabry disease (Orphanet:324)
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease (Orphanet:436242)
Familial isolated hypertrophic cardiomyopathy (Orphanet:155)
Familial isolated pituitary adenoma (Orphanet:314777)
Friedreich ataxia 1 (OMIM:229300)
Gigantism (Orphanet:99725)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Glycogen storage disease due to acid maltase deficiency, infantile onset (Orphanet:308552)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency (Orphanet:137625)
Hurler syndrome (Orphanet:93473)
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation (Orphanet:324525)
Hypertrophic cardiomyopathy due to intensive athletic training (Orphanet:217601)
Isolated sedoheptulokinase deficiency (ORPHA:440713)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Left ventricular noncompaction (Orphanet:54260)
Left ventricular noncompaction 1 (OMIM:604169)
Left ventricular noncompaction 10 (OMIM:615396)
Leprechaunism (Orphanet:508)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 (OMIM:613153)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism (Orphanet:280679)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome (Orphanet:457185)
Nephronophthisis 3 (OMIM:604387)
Noonan syndrome with multiple lentigines (Orphanet:500)
Primary hyperoxaluria type 1 (Orphanet:93598)
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome (Orphanet:228012)
Somatotroph adenoma (Orphanet:96256)
Tangier disease (Orphanet:31150)
Vici syndrome (Orphanet:1493)