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Disease Info Card
Congenital Myopathy (disorder)
Information about Congenital Myopathy (disorder): characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Congenital Myopathy (disorder)
Most recent studies have shown that Congenital Myopathy (disorder) shares some biological mechanisms with atrophy, central-core-myopathy-(disorder), congenital-fiber-type-disproportion, congenital-structural-myopathy, dystrophy, malignant-hyperpyrexia-due-to-anesthesia, malignant-paraganglionic-neoplasm, muscle-contracture, muscle-hypotonia, muscle-weakness, muscular-atrophy, muscular-dystrophy, myopathies-nemaline, myopathy, myotonic-dystrophy, neuromuscular-diseases, scoliosis-unspecified, spinal-muscular-atrophy, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Myopathy (disorder), and have been seen in publications frequently: Autophagy, Cardiac Conduction, Cell Activation, Cell Adhesion, Cell Migration, Clathrin-mediated Endocytosis, Endocytosis, Exocytosis, Flight, Glycolysis, Innervation, Localization, Muscle Atrophy, Muscle Contraction, Pathogenesis, Reflex, Regeneration, Response To Caffeine, Skeletal Muscle Contraction, Transport
Quite a number of genes have been found to play important roles in Congenital Myopathy (disorder), such as ACTA1, BIN1, CHKA, CHKB, DES, DMD, DNM2, MTM1, MYH14, MYOG, NEB, RUNX2, RYR1, TPM1, TPM2, TPM3, VIM. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.