Becker Muscular Dystrophy

About the Disease
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 MIF Mediated Glucocorticoid Regulation. The drugs Carvedilol and Ramipril have been mentioned in the context of this disorder. Affiliated tissues include bone marrow, heart and bone, and related phenotypes are homeostasis/metabolism and muscle

Common Targets
Eukaryotic translation initiation factor 2-alpha kinase (nonspecified subtype) | IL1B | G7124 | PDE5A | NF-kappaB (NFkB) | FASN | CLCN1 | Histone deacetylase (nonspecified subtype) | FKRP | ALOX5 | UTRN | DMD | RYR1

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