Hypertrophic cardiomyopathy
Symptom Information:
Symptom ID: | HPO:0001639 | |||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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 the myocardium(HPO:0001637) Cardiomyopathy(HPO:0001638) Hypertrophic cardiomyopathy(HPO:0001639) MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Cardiac and vascular disorders congenital(MedDRA:10007510) Cardiac septal defects congenital(MedDRA:10007607) Hypertrophic cardiomyopathy(HPO:0001639) |
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Database Frequency: | 137 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY | (OMIM:231530) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Alpha-crystallinopathy | (Orphanet:98910) |
Alström syndrome | (Orphanet:64) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Autosomal recessive limb-girdle muscular dystrophy type 2F | (Orphanet:219) |
Autosomal recessive limb-girdle muscular dystrophy type 2G | (Orphanet:34514) |
Autosomal recessive optic atrophy, OPA7 type | (Orphanet:227976) |
Barth syndrome | (Orphanet:111) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 1 | (OMIM:604377) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CARDIOFACIOCUTANEOUS SYNDROME 3 | (OMIM:615279) |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 | (OMIM:617047) |
COENZYME Q10 DEFICIENCY, PRIMARY, 1 | (OMIM:607426) |
COENZYME Q10 DEFICIENCY, PRIMARY, 7 | (OMIM:616276) |
CORNELIA DE LANGE SYNDROME 2 | (OMIM:300590) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
Cardiomyopathy, dilated, 1D | (OMIM:601494) |
Cardiomyopathy, dilated, 1KK | (OMIM:615248) |
Cardiomyopathy, dilated, 1M | (OMIM:607482) |
Cardiomyopathy, familial hypertrophic, 1 | (OMIM:192600) |
Cardiomyopathy, familial hypertrophic, 10 | (OMIM:608758) |
Cardiomyopathy, familial hypertrophic, 11 | (OMIM:612098) |
Cardiomyopathy, familial hypertrophic, 12 | (OMIM:612124) |
Cardiomyopathy, familial hypertrophic, 13 | (OMIM:613243) |
Cardiomyopathy, familial hypertrophic, 14 | (OMIM:613251) |
Cardiomyopathy, familial hypertrophic, 15 | (OMIM:613255) |
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, 6 | (OMIM:600858) |
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) |
Cardiomyopathy-hypotonia-lactic acidosis syndrome | (Orphanet:91130) |
Cardiomyopathy-renal anomalies | (Orphanet:90022) |
Carnitine uptake deficiency | (Orphanet:158) |
Cirrhotic cardiomyopathy | (Orphanet:57777) |
Combined oxidative phosphorylation defect type 15 | (Orphanet:319524) |
Combined oxidative phosphorylation defect type 17 | (Orphanet:369913) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Combined oxidative phosphorylation defect type 9 | (Orphanet:319509) |
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome | (Orphanet:1369) |
Congenital dyserythropoietic anemia type IV | (Orphanet:293825) |
Costello syndrome | (Orphanet:3071) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Desminopathy | (Orphanet:98909) |
Diabetic embryopathy | (Orphanet:1926) |
Encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome | (Orphanet:319678) |
Fabry disease | (Orphanet:324) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Fatal infantile cytochrome C oxidase deficiency | (Orphanet:1561) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Friedreich ataxia 1 | (OMIM:229300) |
GM1 gangliosidosis | (Orphanet:354) |
GM1 gangliosidosis type 1 | (Orphanet:79255) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Glycogen storage disease due to glycogen branching enzyme deficiency | (Orphanet:367) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hyaline body myopathy | (Orphanet:53698) |
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency | (Orphanet:71212) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Hypertrophic cardiomyopathy due to intensive athletic training | (Orphanet:217601) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency | (Orphanet:352563) |
Isolated ATP synthase deficiency | (Orphanet:254913) |
Isolated CoQ-cytochrome C reductase deficiency | (Orphanet:1460) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isolated cytochrome C oxidase deficiency | (Orphanet:254905) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Leigh syndrome | (Orphanet:506) |
Leprechaunism | (Orphanet:508) |
Lethal polymalformative syndrome, Boissel type | (Orphanet:210144) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
MELAS | (Orphanet:550) |
MERRF | (Orphanet:551) |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1 | (OMIM:604273) |
MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 3 | (OMIM:614053) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 12 (CARDIOMYOPATHIC TYPE) | (OMIM:615418) |
MYOPATHY, AUTOPHAGIC VACUOLAR, INFANTILE-ONSET | (OMIM:609500) |
Malonic aciduria | (Orphanet:943) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Maternally-inherited cardiomyopathy and hearing loss | (Orphanet:1349) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies | (Orphanet:369897) |
Mitochondrial disease with hypertrophic cardiomyopathy | (Orphanet:217587) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency | (Orphanet:314637) |
Mucolipidosis type 2 | (Orphanet:576) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Myopathy, lactic acidosis, and sideroblastic anemia 1; MLASA1 | (OMIM:600462) |
Myopathy, lactic acidosis, and sideroblastic anemia 2; MLASA2 | (OMIM:613561) |
NOONAN SYNDROME 1 | (OMIM:163950) |
NOONAN SYNDROME 4 | (OMIM:610733) |
NOONAN SYNDROME 5 | (OMIM:611553) |
NOONAN SYNDROME 6 | (OMIM:613224) |
NOONAN SYNDROME 8 | (OMIM:615355) |
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome | (Orphanet:457185) |
Nephronophthisis 16 | (OMIM:615382) |
Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome | (Orphanet:228012) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Pyruvate dehydrogenase lipoic acid synthetase deficiency | (OMIM:614462) |
Short chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:35123) |
Tetrasomy 12p | (Orphanet:884) |
Timothy syndrome | (Orphanet:65283) |
Tyrosinemia type 1 | (Orphanet:882) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Vici syndrome | (Orphanet:1493) |
Wolfram syndrome | (Orphanet:3463) |
X-linked myopathy with postural muscle atrophy | (Orphanet:178461) |
[DEL] SENGERS SYNDROME | (OMIM:212350) |