Cardiomyopathy
Symptom Information:
Symptom ID: | HPO:0001638 | ||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): | |||||||||||||||||||||||||||||||||||||||||||||||
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) |
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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) |