Cardiomyopathy, Dilated, 1m (CMD1M)

Alias:
Dilated Cardiomyopathy 1m
Cmd1m
Cardiomyopathy, Dilated, Type 1m
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Cardiomyopathy, Dilated, 1m, also known as dilated cardiomyopathy 1m, is related to cardiomyopathy, dilated, 1a and autosomal recessive limb-girdle muscular dystrophy type 2g. An important gene associated with Cardiomyopathy, Dilated, 1m is CSRP3 (Cysteine And Glycine Rich Protein 3), and among its related pathways/superpathways are Cardiac conduction and Striated muscle contraction pathway. Affiliated tissues include heart, and related phenotypes are dilated cardiomyopathy and reduced left ventricular ejection fraction
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Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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16
86
11

Medical Symptom

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Description
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Gene & Mutation

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Disease Model

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MGI
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Publications
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References Literature

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