Dilated cardiomyopathy

Symptom Information:

Symptom ID: HPO:0001644
Synonyms:
Cardiomyopathy, dilated [HPO:0001644]
Congestive cardiomyopathy (disorder) [Orphanet:34540]
Cardiomyopathy, Dilated [Orphanet:34540]
Cardiomyopathy, dilated [OMIM:Cardiomyopathy, dilated]
Dilated cardiomyopathy [OMIM:Dilated cardiomyopathy]
Cardiomyopathy/hypertrophic/dilated [Orphanet:34540]
Congestive cardiomyopathy [Orphanet:34540]
Congestive cardiomyopathy [MedDRA:10056370]
COCM Congestive (dilated) cardiomyopathy [MedDRA:10056370]
Congestive (dilated) cardiomyopathy [MedDRA:10056370]
Dilated cardiomyopathy [MedDRA:10056370]
Non-ischaemic dilated cardiomyopathy [MedDRA:10056370]
Non-ischemic dilated cardiomyopathy [MedDRA:10056370]
Cardiomyopathy, dilated (in 1 patient) [OMIM:Cardiomyopathy, dilated (in 1 patient)]
Dilated cardiomyopathy (in a subset of patients) [OMIM:Dilated cardiomyopathy (in a subset of patients)]
Dilated cardiomyopathy (in some patients) [OMIM:Dilated cardiomyopathy (in some patients)]
Dilated cardiomyopathy (infancy) [OMIM:Dilated cardiomyopathy (infancy)]
Dilated cardiomyopathy (less common) [OMIM:Dilated cardiomyopathy (less common)]
Dilated cardiomyopathy (occurs in about 50%) [OMIM:Dilated cardiomyopathy (occurs in about 50%)]
Dilated cardiomyopathy (onset in second decade) [OMIM:Dilated cardiomyopathy (onset in second decade)]
Dilated cardiomyopathy (rare) [OMIM:Dilated cardiomyopathy (rare)]
Dilated cardiomyopathy (reported in 1 patient) [OMIM:Dilated cardiomyopathy (reported in 1 patient)]
Dilated cardiomyopathy (variable) [OMIM:Dilated cardiomyopathy (variable)]
Quality:
Cross references:
Orphanet:34540 "Cardiomyopathy/hypertrophic/dilated" [Orphanet:34540]
OMIM: "Cardiomyopathy, dilated" [OMIM:Cardiomyopathy, dilated]
OMIM: "Dilated cardiomyopathy" [OMIM:Dilated cardiomyopathy]
OMIM: "Cardiomyopathy, dilated (in 1 patient)" [OMIM:Cardiomyopathy, dilated (in 1 patient)]
OMIM: "Dilated cardiomyopathy (in a subset of patients)" [OMIM:Dilated cardiomyopathy (in a subset of patients)]
OMIM: "Dilated cardiomyopathy (in some patients)" [OMIM:Dilated cardiomyopathy (in some patients)]
OMIM: "Dilated cardiomyopathy (infancy)" [OMIM:Dilated cardiomyopathy (infancy)]
OMIM: "Dilated cardiomyopathy (less common)" [OMIM:Dilated cardiomyopathy (less common)]
OMIM: "Dilated cardiomyopathy (occurs in about 50%)" [OMIM:Dilated cardiomyopathy (occurs in about 50%)]
OMIM: "Dilated cardiomyopathy (onset in second decade)" [OMIM:Dilated cardiomyopathy (onset in second decade)]
OMIM: "Dilated cardiomyopathy (rare)" [OMIM:Dilated cardiomyopathy (rare)]
OMIM: "Dilated cardiomyopathy (reported in 1 patient)" [OMIM:Dilated cardiomyopathy (reported in 1 patient)]
OMIM: "Dilated cardiomyopathy (variable)" [OMIM:Dilated cardiomyopathy (variable)]
UMLS:C0007193 "Cardiomyopathy, Dilated" [Orphanet:34540]
Is a (Direct Parents):
Orphanet Hypertrophic cardiomyopathy
Orphanet Structural anomalies of the cardio-circulatory system
HPO         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)
                      Dilated cardiomyopathy(HPO:0001644)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Dilated cardiomyopathy(HPO:0001644)
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)