Dilated Cardiomyopathy (DCM)

Alias:
Familial Dilated Cardiomyopathy
Primary Dilated Cardiomyopathy
Primary Familial Dilated Cardiomyopathy
Idiopathic Dilation Cardiomyopathy
Congestive Cardiomyopathy
Cardiomyopathy, Dilated
Primary Idiopathic Dilated Cardiomyopathy
Congestive Idiopathic Cardiomyopathy
Cardiomyopathy, Familial Idiopathic
Familial Idiopathic Cardiomyopathy
Cocm - [congestive Cardiomyopathy]
Dilated-Hypokinetic Cardiomyopathy
Idiopathic Dilated Cardiomyopathy
Dilated Congestive Cardiomyopathy
Ccm - [congestive Cardiomyopathy]
Chronic Dilated Cardiomyopathy
Dcm - [dilated Cardiomyopathy]
Idiopathic Cardiomegaly
Fdc
Dcm
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Dilated Cardiomyopathy, also known as familial dilated cardiomyopathy, is related to familial isolated dilated cardiomyopathy and cardiomyopathy, dilated, 1a. An important gene associated with Dilated Cardiomyopathy is LMNA (Lamin A/C), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Cardiac conduction. The drugs Verapamil and Digoxin have been mentioned in the context of this disorder. Affiliated tissues include Heart and bone marrow, and related phenotypes are muscle and growth/size/body region
Related ID:
MESH:D002311
ICD11:167155244

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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All ages
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413
4522
402

Medical Symptom

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Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

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CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

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PMID
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IF
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