Cardiomyopathy

Symptom Information:

Symptom ID: HPO:0001638
Synonyms:
Myocardium anomaly [Orphanet:34560]
Cardiomyopathy (disorder) [Orphanet:34560]
Myocardial disease (disorder) [Orphanet:34560]
Cardiomyopathies [Orphanet:34560]
Cardiomyopathy [OMIM:Cardiomyopathy]
Myocardium anomalies/myocarditis [Orphanet:34560]
Cardiomyopathy [Orphanet:34560]
Cardiomyopathy [MedDRA:10007636]
Cardiomyopathy in other diseases classified elsewhere [MedDRA:10007636]
Cardiomyopathy NOS [MedDRA:10007636]
Cardiomyopathy primary NOS [MedDRA:10007636]
Cardiomyopathy secondary NOS [MedDRA:10007636]
Degeneration myocardial [MedDRA:10007636]
Myocardial degeneration [MedDRA:10007636]
Myocardial disorder [MedDRA:10007636]
Myocardosis [MedDRA:10007636]
Nutritional and metabolic cardiomyopathy [MedDRA:10007636]
Obscure cardiomyopathy of Africa [MedDRA:10007636]
Other primary cardiomyopathies [MedDRA:10007636]
Secondary cardiomyopathy, unspecified [MedDRA:10007636]
Non-ischaemic cardiomyopathy [MedDRA:10007636]
Non-ischemic cardiomyopathy [MedDRA:10007636]
Cardiomyopathy primary [MedDRA:10007636]
Cardiomyopathy secondary [MedDRA:10007636]
Myocardiodystrophy [MedDRA:10007636]
Cardiomyopathy (1 patient) [OMIM:Cardiomyopathy (1 patient)]
Cardiomyopathy (CVS+) [OMIM:Cardiomyopathy (CVS+)]
Cardiomyopathy (in 2 of 4 patients from 1 family) [OMIM:Cardiomyopathy (in 2 of 4 patients from 1 family)]
Cardiomyopathy (in a subset of patients) [OMIM:Cardiomyopathy (in a subset of patients)]
Cardiomyopathy (in some patients) [OMIM:Cardiomyopathy (in some patients)]
Cardiomyopathy (in some) [OMIM:Cardiomyopathy (in some)]
Cardiomyopathy (less common) [OMIM:Cardiomyopathy (less common)]
Cardiomyopathy (rare) [OMIM:Cardiomyopathy (rare)]
Cardiomyopathy (reported in 1 family) [OMIM:Cardiomyopathy (reported in 1 family)]
Cardiomyopathy (reported in 1 patient) [OMIM:Cardiomyopathy (reported in 1 patient)]
Cardiomyopathy (reported in 2 patients) [OMIM:Cardiomyopathy (reported in 2 patients)]
Cardiomyopathy (severe form) [OMIM:Cardiomyopathy (severe form)]
Cardiomyopathy (type II, congenital) [OMIM:Cardiomyopathy (type II, congenital)]
Cardiomyopathy (uncommon) [OMIM:Cardiomyopathy (uncommon)]
Cardiomyopathy (variable) [OMIM:Cardiomyopathy (variable)]
No cardiomyopathy [OMIM:No cardiomyopathy]
Myocarditis [MedDRA:10028606]
Myocarditis (disorder) [Orphanet:34560]
Myocarditis [Orphanet:34560]
Myocardial disorders [MedDRA:10028593]
Cardiomyopathies [MedDRA:10007635]
Quality:
Cross references:
HPO:0001637 "Abnormality of the myocardium" [Orphanet:34560]
Orphanet:34560 "Myocardium anomalies/myocarditis" [Orphanet:34560]
OMIM: "Cardiomyopathy" [OMIM:Cardiomyopathy]
OMIM: "Cardiomyopathy (1 patient)" [OMIM:Cardiomyopathy (1 patient)]
OMIM: "Cardiomyopathy (CVS+)" [OMIM:Cardiomyopathy (CVS+)]
OMIM: "Cardiomyopathy (in 2 of 4 patients from 1 family)" [OMIM:Cardiomyopathy (in 2 of 4 patients from 1 family)]
OMIM: "Cardiomyopathy (in a subset of patients)" [OMIM:Cardiomyopathy (in a subset of patients)]
OMIM: "Cardiomyopathy (in some patients)" [OMIM:Cardiomyopathy (in some patients)]
OMIM: "Cardiomyopathy (in some)" [OMIM:Cardiomyopathy (in some)]
OMIM: "Cardiomyopathy (less common)" [OMIM:Cardiomyopathy (less common)]
OMIM: "Cardiomyopathy (rare)" [OMIM:Cardiomyopathy (rare)]
OMIM: "Cardiomyopathy (reported in 1 family)" [OMIM:Cardiomyopathy (reported in 1 family)]
OMIM: "Cardiomyopathy (reported in 1 patient)" [OMIM:Cardiomyopathy (reported in 1 patient)]
OMIM: "Cardiomyopathy (reported in 2 patients)" [OMIM:Cardiomyopathy (reported in 2 patients)]
OMIM: "Cardiomyopathy (severe form)" [OMIM:Cardiomyopathy (severe form)]
OMIM: "Cardiomyopathy (type II, congenital)" [OMIM:Cardiomyopathy (type II, congenital)]
OMIM: "Cardiomyopathy (uncommon)" [OMIM:Cardiomyopathy (uncommon)]
OMIM: "Cardiomyopathy (variable)" [OMIM:Cardiomyopathy (variable)]
OMIM: "No cardiomyopathy" [OMIM:No cardiomyopathy]
UMLS:C0878544 "Cardiomyopathy" [HPO:0001638]
UMLS:C0878544 "Cardiomyopathies" [Orphanet:34560]
UMLS:C0027059 "Myocarditis" [Orphanet:34560]
Is a (Direct Parents):
HPO         Abnormality of the myocardium
MedDRA Cardiac disorders
Orphanet Abnormality of the myocardium
Orphanet Structural anomalies of the cardio-circulatory system
HPO         Noncompaction cardiomyopathy
MedDRA Abnormality of the myocardium
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)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Cardiomyopathy(HPO:0001638)
    Cardiomyopathy(HPO:0001638)
Database Frequency: 192 / 7739
Resource:

All diseases associated with this symptom:

16q24.3 microdeletion syndrome (Orphanet:261250)
1p36 deletion syndrome (Orphanet:1606)
8p23.1 microdeletion syndrome (Orphanet:251071)
AL amyloidosis (Orphanet:85443)
ALG1-CDG (Orphanet:79327)
ATAXIA, DEAFNESS, AND CARDIOMYOPATHY (OMIM:208750)
ATTRV122I amyloidosis (Orphanet:85451)
Acromegaly (Orphanet:963)
Acyl-CoA dehydrogenase 9 deficiency (Orphanet:99901)
Alpers syndrome (Orphanet:726)
Alpha-N-acetylgalactosaminidase deficiency type 1 (Orphanet:79279)
Alpha-N-acetylgalactosaminidase deficiency type 3 (Orphanet:79281)
Arterial calcification, generalized, of infancy, 1 (OMIM:208000)
Arterial tortuosity syndrome (Orphanet:3342)
Arthrogryposis due to muscular dystrophy (Orphanet:1155)
Ataxia with vitamin E deficiency (Orphanet:96)
Atrial standstill 2 (OMIM:615745)
Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Autosomal recessive limb-girdle muscular dystrophy type 2I (Orphanet:34515)
Autosomal recessive limb-girdle muscular dystrophy type 2J (Orphanet:140922)
Autosomal recessive limb-girdle muscular dystrophy type 2K (Orphanet:86812)
Autosomal recessive limb-girdle muscular dystrophy type 2T (Orphanet:363623)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
Barth syndrome (Orphanet:111)
Beckwith-Wiedemann syndrome (Orphanet:116)
Beta-thalassemia (Orphanet:848)
Beta-thalassemia major (Orphanet:231214)
Bone dysplasia, lethal Holmgren type (Orphanet:1842)
CARDIOMYOPATHY ASSOCIATED WITH MYOPATHY AND SUDDEN DEATH (OMIM:212130)
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS (OMIM:606842)
CEDNIK syndrome (Orphanet:66631)
COG7-CDG (Orphanet:79333)
CYCLIC VOMITING SYNDROME (OMIM:500007)
Camurati-Engelmann disease (Orphanet:1328)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Cardiomyopathy, familial hypertrophic, 12 (OMIM:612124)
Cardiomyopathy, fatal fetal, due to myocardial calcification (OMIM:300829)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine palmitoyl transferase II deficiency (Orphanet:157)
Carnitine palmitoyl transferase II deficiency, severe infantile form (Orphanet:228305)
Carnitine-acylcarnitine translocase deficiency (Orphanet:159)
Cartilage-hair hypoplasia (Orphanet:175)
Cataract - intellectual deficit - hypogonadism (Orphanet:1387)
Choreoacanthocytosis (Orphanet:2388)
Cockayne syndrome (Orphanet:191)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Combined oxidative phosphorylation defect type 15 (Orphanet:319524)
Combined oxidative phosphorylation deficiency type 23 (ORPHA:444013)
Congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome (Orphanet:1369)
Congenital disorder of glycosylation (Orphanet:137)
Congenital heart block (Orphanet:60041)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Costello syndrome (Orphanet:3071)
D-2-@HYDROXYGLUTARIC ACIDURIA 1 (OMIM:600721)
D-2-@HYDROXYGLUTARIC ACIDURIA 2 (OMIM:613657)
D-2-hydroxyglutaric aciduria (Orphanet:79315)
Desminopathy (Orphanet:98909)
Diabetic embryopathy (Orphanet:1926)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
Distal myopathy with posterior leg and anterior hand involvement (Orphanet:63273)
Duchenne and Becker muscular dystrophy (Orphanet:262)
Dystrophic epidermolysis bullosa (Orphanet:303)
EMERY-DREIFUSS MUSCULAR DYSTROPHY 5, AUTOSOMAL DOMINANT (OMIM:612999)
ENDOCARDIAL FIBROELASTOSIS AND COARCTATION OF ABDOMINAL AORTA (OMIM:226100)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy,and cataracts (OMIM:225740)
Endomyocardial fibroelastosis (Orphanet:2022)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Fabry disease (Orphanet:324)
Familial amyloid polyneuropathy (Orphanet:85447)
Familial amyloidosis, Finnish type (Orphanet:85448)
Familial cutaneous collagenoma (Orphanet:53296)
Familial isolated pituitary adenoma (Orphanet:314777)
Fanconi anemia (Orphanet:84)
Fetal parvovirus syndrome (Orphanet:295)
Friedreich ataxia 1 (OMIM:229300)
Friedreich ataxia 2 (OMIM:601992)
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT (OMIM:610100)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 3 (Orphanet:77261)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Gigantism (Orphanet:99725)
Glycogen storage disease due to LAMP-2 deficiency (Orphanet:34587)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form (Orphanet:308712)
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form (Orphanet:308684)
Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form (Orphanet:308698)
Glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form (Orphanet:308670)
Glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form (Orphanet:308655)
Glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form (Orphanet:308638)
Glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form (Orphanet:308621)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency (Orphanet:137625)
HEC syndrome (Orphanet:2119)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
His bundle tachycardia (Orphanet:3283)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Incessant infant ventricular tachycardia (Orphanet:45453)
Indomethacin embryofetopathy (Orphanet:1909)
Infantile Refsum disease (Orphanet:772)
Infantile spasms - broad thumbs (Orphanet:3173)
Juvenile dermatomyositis (Orphanet:93672)
Kearns-Sayre syndrome (Orphanet:480)
LMNA-related cardiocutaneous progeria syndrome (Orphanet:363618)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Lethal infantile mitochondrial myopathy (Orphanet:254857)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MELAS (Orphanet:550)
MERRF (Orphanet:551)
MUSCULAR DYSTROPHY, CARDIAC TYPE (OMIM:309930)
MUSCULAR DYSTROPHY, SCAPULOHUMERAL (OMIM:600416)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 1 (OMIM:613155)
Maternally-inherited diabetes and deafness (Orphanet:225)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
Microcephaly-cardiomyopathy syndrome (Orphanet:2515)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Mitochondrial trifunctional protein deficiency (Orphanet:746)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mulibrey nanism (Orphanet:2576)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Myopathy due to calsequestrin and SERCA1 protein overload (Orphanet:88635)
Myotilin-related myofibrillar myopathy without spheroid body (Orphanet:98911)
Naxos disease (Orphanet:34217)
Neurofibromatosis - Noonan syndrome (Orphanet:638)
Neutral lipid storage myopathy (Orphanet:98908)
Noonan syndrome with multiple lentigines (Orphanet:500)
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia (Orphanet:363972)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay (Orphanet:88643)
PMM2-CDG (Orphanet:79318)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Penoscrotal transposition (Orphanet:2842)
Phosphoribosylpyrophosphate synthetase superactivity (Orphanet:3222)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polymyositis (Orphanet:732)
Primary lipodystrophy (Orphanet:90970)
Primary systemic amyloidosis (Orphanet:314701)
Propionic acidemia (Orphanet:35)
Pseudoxanthoma elasticum (Orphanet:758)
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency (Orphanet:88618)
REFSUM DISEASE, CLASSIC (OMIM:266500)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Refsum disease (Orphanet:773)
SIDEROBLASTIC ANEMIA WITH B-CELL IMMUNODEFICIENCY, PERIODIC FEVERS,AND DEVELOPMENTAL DELAY (OMIM:616084)
Scheie syndrome (Orphanet:93474)
Scleroderma (Orphanet:801)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Sialidosis type 1 (Orphanet:812)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Somatotroph adenoma (Orphanet:96256)
Steinert myotonic dystrophy (Orphanet:273)
Takayasu arteritis (Orphanet:3287)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Toriello-Carey syndrome (Orphanet:3338)
Transaldolase deficiency (Orphanet:101028)
Triose phosphate-isomerase deficiency (Orphanet:868)
URUGUAY FACIOCARDIOMUSCULOSKELETAL SYNDROME (OMIM:300280)
Usher syndrome (Orphanet:886)
VENTRICULAR TACHYCARDIA, FAMILIAL (OMIM:192605)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)
Vici syndrome (Orphanet:1493)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)
WOLFF-PARKINSON-WHITE SYNDROME (OMIM:194200)
Williams syndrome (Orphanet:904)
Wilson disease (Orphanet:905)
Wolfram syndrome 1 (OMIM:222300)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome (Orphanet:65282)
Yunis-Varon syndrome (Orphanet:3472)
ZASP-related myofibrillar myopathy (Orphanet:98912)
Zimmermann-Laband syndrome (Orphanet:3473)
[DEL] COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 23 (OMIM:616198)
[DEL] MUSCULAR DYSTROPHY, BECKER TYPE (OMIM:300376)