Duchenne Muscular Dystrophy

About the Disease
Muscular Dystrophy, Duchenne Type, also known as duchenne muscular dystrophy, is related to muscular dystrophy, becker type and facioscapulohumeral muscular dystrophy 1, and has symptoms including waddling gait and weakness. An important gene associated with Muscular Dystrophy, Duchenne Type is DMD (Dystrophin), and among its related pathways/superpathways are Cell differentiation - expanded index and miRNAs involvement in the immune response in sepsis. The drugs Carvedilol and Ramipril have been mentioned in the context of this disorder. Affiliated tissues include Adipose and Umbilical Cord, and related phenotypes are scoliosis and respiratory insufficiency

Common Targets
KDR | MAS1L | G3630 | G7124 | Calpain (nonspecified subtype) | IL1B | Mechanosensitive Ion Channel | Estrogen receptor (nonspecified subtype) | C9orf72 | VIM | Cyclophilins (nonspecified subtype) | G367 | DYRK1A | CD40 | PCDHGC5 | Eukaryotic translation initiation factor 2-alpha kinase (nonspecified subtype) | PPARD | CCN2 | PDE9A | MCOLN1 | G7015 | Reverse transcriptase (Telomerase) | SLC6A4 | CLK4 | NF-kappaB (NFkB) | RYR2 | XPO1 | PDE5A | PIEZO1 | MIR21 | Platelet-Derived Growth Factor Receptor (nonspecified subtype) | Myosin Class II (nonspecified subtype) | ITGA4 | FASN | INHBA | MYH2 | Proteasome Complex | HCRTR2 | CHIA | Prostanoid TP receptor (nonspecified subtype) | G196 | Histone deacetylase (nonspecified subtype) | CDK1/Cyclin B | CRBN | AP-1 Transcription Factor Complex | N-Terminal Acetyltransferase A (NatA) Complex | Transforming growth factor beta (nonspecified subtype) | SNED1 | LCT | Poly [ADP-ribose] polymerase (nonspecified subtype) | ACVR1B | CDK2/Cyclin A | CYP19A1 | SLC5A1 | Cyclooxygenase (COX) (nonspecified subtype) | CLK1 | LAMA1 | FKRP | ALOX5 | MSTN | EHMT2 | GLP1R | G5970 | SLC6A3 | MAOB | LTBP4 | Myosin (nonspecified subtype) | Angiotensin receptor (AT) (nonspecified subtype) | Cyclin A (nonspecified subtype) | CDK1 | JAML | MAS1 | G595 | ATF6 | SGCA | EPRS1 | ENOX2 | UTRN | DMD | GSPT1 | G3620 | Phosphodiesterase (nonspecified subtype) | HPGDS | PER3 | PPARG | MIR128-1 | PPARA | Calcium channel (nonspecified subtype) | CDK2 | CDK4 | Melanocortin receptor (nonspecified subtype) | SPP1 | SNCA | NR3C1 | FAP | G142 | Protein kinase C (nonspecified subtype) | CDK4/Cyclin D1 | G5743 | SLN | TFRC | RYR1 | PLCB3 | Cyclin B (nonspecified subtype) | Tubulin | SLC6A2 | PREP | MIRLET7C | PTGS1 | ACHE | YARS2 | G3569 | DYNLT5 | IKBKB | SLC9A1 | F9 | FLT1 | DYSF | PIEZO2

Note: If you'd like to get a target analysis report for Duchenne Muscular Dystrophy, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Duchenne Muscular Dystrophy at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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