Dilated cardiomyopathy
Symptom Information:
Symptom ID: | HPO:0001644 | |||||||||||||||||||||||
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) Dilated cardiomyopathy(HPO:0001644) MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) Dilated cardiomyopathy(HPO:0001644) |
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Database Frequency: | 141 / 7739 | |||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY | (OMIM:231530) |
3-methylglutaconic aciduria type 4 | (Orphanet:67048) |
AL amyloidosis | (Orphanet:85443) |
Acyl-CoA dehydrogenase 9 deficiency | (Orphanet:99901) |
Alström syndrome | (Orphanet:64) |
Atrial standstill 2 | (OMIM:615745) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal recessive Emery-Dreifuss muscular dystrophy | (Orphanet:98855) |
Autosomal recessive limb-girdle muscular dystrophy type 2B | (Orphanet:268) |
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 limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2M | (Orphanet:206554) |
Barth syndrome | (Orphanet:111) |
Becker muscular dystrophy | (Orphanet:98895) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction | (OMIM:612158) |
Cardiomyopathy, dilated, 1B | (OMIM:600884) |
Cardiomyopathy, dilated, 1BB | (OMIM:612877) |
Cardiomyopathy, dilated, 1CC | (OMIM:613122) |
Cardiomyopathy, dilated, 1D | (OMIM:601494) |
Cardiomyopathy, dilated, 1DD | (OMIM:613172) |
Cardiomyopathy, dilated, 1E | (OMIM:601154) |
Cardiomyopathy, dilated, 1EE | (OMIM:613252) |
Cardiomyopathy, dilated, 1FF | (OMIM:613286) |
Cardiomyopathy, dilated, 1G | (OMIM:604145) |
Cardiomyopathy, dilated, 1GG | (OMIM:613642) |
Cardiomyopathy, dilated, 1H | (OMIM:604288) |
Cardiomyopathy, dilated, 1I | (OMIM:604765) |
Cardiomyopathy, dilated, 1II | (OMIM:615184) |
Cardiomyopathy, dilated, 1JJ | (OMIM:615235) |
Cardiomyopathy, dilated, 1K | (OMIM:605582) |
Cardiomyopathy, dilated, 1KK | (OMIM:615248) |
Cardiomyopathy, dilated, 1L | (OMIM:606685) |
Cardiomyopathy, dilated, 1M | (OMIM:607482) |
Cardiomyopathy, dilated, 1O | (OMIM:608569) |
Cardiomyopathy, dilated, 1P | (OMIM:609909) |
Cardiomyopathy, dilated, 1Q | (OMIM:609915) |
Cardiomyopathy, dilated, 1R | (OMIM:613424) |
Cardiomyopathy, dilated, 1T | (OMIM:613740) |
Cardiomyopathy, dilated, 1U | (OMIM:613694) |
Cardiomyopathy, dilated, 1V | (OMIM:613697) |
Cardiomyopathy, dilated, 1W | (OMIM:611407) |
Cardiomyopathy, dilated, 1X | (OMIM:611615) |
Cardiomyopathy, dilated, 1Y | (OMIM:611878) |
Cardiomyopathy, dilated, 1Z | (OMIM:611879) |
Cardiomyopathy, dilated, 1nn | (OMIM:615916) |
Cardiomyopathy, dilated, 2A | (OMIM:611880) |
Cardiomyopathy, dilated, 2B | (OMIM:614672) |
Cardiomyopathy, dilated, 3B | (OMIM:302045) |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and toothagenesis | (OMIM:615821) |
Cardiomyopathy, familial hypertrophic, 2 | (OMIM:115195) |
Cardiomyopathy, familial hypertrophic, 9 | (OMIM:613765) |
Cardiomyopathy-cataract-hip spine disease | (Orphanet:1345) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Carnitine uptake deficiency | (Orphanet:158) |
Combined oxidative phosphorylation defect type 17 | (Orphanet:369913) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital fiber-type disproportion myopathy | (Orphanet:2020) |
Congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect | (Orphanet:280671) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
DK1-CDG | (Orphanet:91131) |
DPM3-CDG | (Orphanet:263494) |
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 | (OMIM:613989) |
Desminopathy | (Orphanet:98909) |
Dilated cardiomyopathy with ataxia | (Orphanet:66634) |
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | (Orphanet:2229) |
Duchenne muscular dystrophy | (Orphanet:98896) |
Early-onset myopathy with fatal cardiomyopathy | (Orphanet:289377) |
Emery-Dreifuss muscular dystrophy | (Orphanet:261) |
Endomyocardial fibroelastosis | (Orphanet:2022) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Familial atrial fibrillation | (Orphanet:334) |
Familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease | (Orphanet:436242) |
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation | (Orphanet:300751) |
Familial dyskinesia and facial myokymia | (Orphanet:324588) |
Familial isolated dilated cardiomyopathy | (Orphanet:154) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
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 glycogen branching enzyme deficiency | (Orphanet:367) |
Heart-hand syndrome, Slovenian type | (Orphanet:168796) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis, type 2A | (OMIM:602390) |
His bundle tachycardia | (Orphanet:3283) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Hyaline body myopathy | (Orphanet:53698) |
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency | (Orphanet:71212) |
Hypertaurinuric cardiomyopathy | (OMIM:145350) |
Idiopathic giant cell myocarditis | (Orphanet:329874) |
Isobutyryl-CoA dehydrogenase deficiency | (Orphanet:79159) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
Johanson-Blizzard syndrome | (Orphanet:2315) |
Laing distal myopathy | (Orphanet:59135) |
Left ventricular noncompaction 10 | (OMIM:615396) |
Leigh syndrome | (Orphanet:506) |
Lethal congenital contracture syndrome type 2 | (Orphanet:137776) |
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
MELAS | (Orphanet:550) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 | (OMIM:614299) |
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 4 | (OMIM:253800) |
MYOPATHY, CENTRONUCLEAR, 5 | (OMIM:615959) |
MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION, X-LINKED | (OMIM:300580) |
MYOPATHY, REDUCING BODY, X-LINKED, CHILDHOOD-ONSET | (OMIM:300718) |
Maternally-inherited diabetes and deafness | (Orphanet:225) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Microcephaly-cardiomyopathy syndrome | (Orphanet:2515) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial trifunctional protein deficiency | (Orphanet:746) |
Moyamoya disease - short stature - facial dysmorphism - hypergonadotropic hypogonadism | (Orphanet:280679) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Naxos disease | (Orphanet:34217) |
Nemaline myopathy | (Orphanet:607) |
Nephronophthisis-like nephropathy 1 | (OMIM:613159) |
PGM1-CDG | (Orphanet:319646) |
POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY | (OMIM:615895) |
Peripartum cardiomyopathy | (Orphanet:563) |
Polyglucosan body myopathy type 1 | (ORPHA:397937) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Primary systemic amyloidosis | (Orphanet:314701) |
Progressive external ophthalmoplegia - myopathy - emaciation | (Orphanet:352447) |
Sensorineural deafness with dilated cardiomyopathy | (Orphanet:217622) |
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis | (Orphanet:70595) |
Spinocerebellar ataxia with epilepsy | (Orphanet:254881) |
Steinert myotonic dystrophy | (Orphanet:273) |
Symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers | (Orphanet:206546) |
Tubular renal disease-cardiomyopathy syndrome | (Orphanet:73224) |
Vici syndrome | (Orphanet:1493) |
Wolfram syndrome | (Orphanet:3463) |
Wolfram syndrome 1 | (OMIM:222300) |
Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome | (Orphanet:65282) |
X-linked Emery-Dreifuss muscular dystrophy | (Orphanet:98863) |
[DEL] CARDIAC CONDUCTION DISEASE WITH OR WITHOUT DILATED CARDIOMYOPATHY | (OMIM:616117) |