Familial Isolated Dilated Cardiomyopathy

Alias:
Familial or Idiopathic Dilated Cardiomyopathy
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Familial Isolated Dilated Cardiomyopathy, also known as familial or idiopathic dilated cardiomyopathy, is related to cardiomyopathy, dilated, 1a and cardiomyopathy, dilated, 1b. An important gene associated with Familial Isolated Dilated Cardiomyopathy is LMOD2 (Leiomodin 2), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Cardiac conduction. Affiliated tissues include heart, and related phenotypes are dilated cardiomyopathy and sensorineural hearing impairment
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Mit
AD
XL
XLD
AR
All ages
1-9/100000
51
478
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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

Name
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
Journal
Year
IF
No Data Found!
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