Left ventricular hypertrophy
Symptom Information:
| Symptom ID: | HPO:0001712 | |||||||
| Synonyms: |
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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) 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) |
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| 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) |