Congenital Muscular Dystrophy

About the Disease
Muscular Dystrophy, also known as muscular dystrophies, is related to limb-girdle muscular dystrophy and muscular dystrophy, limb-girdle, autosomal recessive 2, and has symptoms including back pain, muscle cramp and myoclonus. An important gene associated with Muscular Dystrophy is DMD (Dystrophin), and among its related pathways/superpathways are DREAM Repression and Dynorphin Expression and Acute viral myocarditis. The drugs Carvedilol and Ramipril have been mentioned in the context of this disorder. Affiliated tissues include skeletal muscle, bone marrow and brain, and related phenotypes are no effect and no effect

Common Targets
POMGNT1 | HRAS | POMT1 | RYR1 | Eukaryotic translation initiation factor 2-alpha kinase (nonspecified subtype) | TOR1AIP1 | TRIP4 | DNM2 | CRPPA | POMT2 | CHKB | COL6A1 | DAG1 | LAMA2 | LAMA1 | FKRP | COL6A2 | TTN | GOSR2 | SYNE1 | ACTA1 | MAS1 | Angiotensin receptor (AT) (nonspecified subtype) | COL6A3 | MSTO1 | GMPPB | DMD | B3GALNT2

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