Hypertrophic cardiomyopathy

Symptom Information:

Symptom ID: HPO:0001639
Synonyms:
Cardiomyopathy, hypertrophic [HPO:0001639]
Hypertrophic cardiomyopathy (disorder) [Orphanet:34540]
Hypertrophic Cardiomyopathy [Orphanet:34540]
Cardiomyopathy, hypertrophic [OMIM:Cardiomyopathy, hypertrophic]
Hypertrophic cardiomyopathy [OMIM:Hypertrophic cardiomyopathy]
Cardiomyopathy/hypertrophic/dilated [Orphanet:34540]
Hypertrophic cardiomyopathy [Orphanet:34540]
Hypertrophic cardiomyopathy [MedDRA:10020871]
HOCM [MedDRA:10020871]
HOCM Hypertrophic obstructive cardiomyopathy [MedDRA:10020871]
Hypertrophic obstructive cardiomyopathy [MedDRA:10020871]
Idiopathic hypertrophic subaortic stenosis [MedDRA:10020871]
IHSS [MedDRA:10020871]
Obstructive cardiomyopathy [MedDRA:10020871]
Hypertrophic cardiomyopathy (1 patient) [OMIM:Hypertrophic cardiomyopathy (1 patient)]
Hypertrophic cardiomyopathy (20%) [OMIM:Hypertrophic cardiomyopathy (20%)]
Hypertrophic cardiomyopathy (associated with mutation in the COX10 and C2ORF64 genes) [OMIM:Hypertrophic cardiomyopathy (associated with mutation in the COX10 and C2ORF64 genes)]
Hypertrophic cardiomyopathy (in a subset of patients) [OMIM:Hypertrophic cardiomyopathy (in a subset of patients)]
Hypertrophic cardiomyopathy (in some patients) [OMIM:Hypertrophic cardiomyopathy (in some patients)]
Hypertrophic cardiomyopathy (reported in 1 patient) [OMIM:Hypertrophic cardiomyopathy (reported in 1 patient)]
Hypertrophic cardiomyopathy (uncommon) [OMIM:Hypertrophic cardiomyopathy (uncommon)]
Hypertrophic obstructive cardiomyopathy [OMIM:Hypertrophic obstructive cardiomyopathy]
Biopsy shows hypertrophic cardiomyocytes [OMIM,du]
Quality:
Cross references:
Orphanet:34540 "Cardiomyopathy/hypertrophic/dilated" [Orphanet:34540]
OMIM: "Cardiomyopathy, hypertrophic" [OMIM:Cardiomyopathy, hypertrophic]
OMIM: "Hypertrophic cardiomyopathy" [OMIM:Hypertrophic cardiomyopathy]
OMIM: "Hypertrophic cardiomyopathy (1 patient)" [OMIM:Hypertrophic cardiomyopathy (1 patient)]
OMIM: "Hypertrophic cardiomyopathy (20%)" [OMIM:Hypertrophic cardiomyopathy (20%)]
OMIM: "Hypertrophic cardiomyopathy (associated with mutation in the COX10 and C2ORF64 genes)" [OMIM:Hypertrophic cardiomyopathy (associated with mutation in the COX10 and C2ORF64 genes)]
OMIM: "Hypertrophic cardiomyopathy (in a subset of patients)" [OMIM:Hypertrophic cardiomyopathy (in a subset of patients)]
OMIM: "Hypertrophic cardiomyopathy (in some patients)" [OMIM:Hypertrophic cardiomyopathy (in some patients)]
OMIM: "Hypertrophic cardiomyopathy (reported in 1 patient)" [OMIM:Hypertrophic cardiomyopathy (reported in 1 patient)]
OMIM: "Hypertrophic cardiomyopathy (uncommon)" [OMIM:Hypertrophic cardiomyopathy (uncommon)]
OMIM: "Hypertrophic obstructive cardiomyopathy" [OMIM:Hypertrophic obstructive cardiomyopathy]
UMLS:C0007194 "Hypertrophic Cardiomyopathy" [Orphanet:34540]
Is a (Direct Parents):
MedDRA Cardiac septal defects congenital
Orphanet Structural anomalies of the cardio-circulatory system
HPO         Cardiomyopathy
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)
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)