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Diseases

Cardiomyopathy, Dilated

cardiomyopathy, dilated

Entity Type
Diseases
Relation Groups
1
Relation Preview
8

Basic Information

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Core Information

Disease Name
Cardiomyopathy, Dilated
Standard Disease Name
cardiomyopathy, dilated
MeSH Tree
No data
ICD-10
I42.0

Identifiers

DO ID
No data
MeSH ID
D002311
OMIM ID
MTHU001652|MTHU019869
UMLS ID
C0007193
HPO ID
No data

Description and Extensions

Description
NCI2016_02D:Cardiomyopathy which is characterized by dilation and contractile dysfunction of the left and right ventricles. It may be idiopathic, or it may result from a myocardial infarction, myocardial infection, or alcohol abuse. It is a cause of congestive heart failure.|MSH2017_2016_08_12:A form of CARDIAC MUSCLE disease that is characterized by ventricular dilation, VENTRICULAR DYSFUNCTION, and HEART FAILURE. Risk factors include SMOKING; ALCOHOL DRINKING; HYPERTENSION; INFECTION; PREGNANCY; and mutations in the LMNA gene encoding LAMIN TYPE A, a NUCLEAR LAMINA protein.|HPO2016_07_04:Dilated cardiomyopathy (DCM) is defined by the presence of left ventricular dilatation and left ventricular systolic dysfunction in the absence of abnormal loading conditions (hypertension, valve disease) or coronary artery disease sufficient to cause global systolic impairment. Right ventricular dilation and dysfunction may be present but are not necessary for the diagnosis. [pmid:17916581]
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