Endomyocardial Fibrosis (EMF)

Alias:
Obscure African Cardiomyopathy
Becker's Disease
African Endomyocardial Fibrosis
Becker Muscular Dystrophy
Endomyocardial Sclerosis
Emf
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Endomyocardial Fibrosis, also known as obscure african cardiomyopathy, is related to myotonia congenita, autosomal recessive and myeloid and lymphoid neoplasms associated with pdgfra rearrangement, and has symptoms including weakness An important gene associated with Endomyocardial Fibrosis is CLCN1 (Chloride Voltage-Gated Channel 1), and among its related pathways/superpathways are ERK Signaling and Akt Signaling. The drugs Ramipril and Carvedilol have been mentioned in the context of this disorder. Affiliated tissues include bone marrow and heart, and related phenotypes are muscle and homeostasis/metabolism
Related ID:
MESH:D004719

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
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Unknown
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25
332
145

Medical Symptom

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Description
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No data available

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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