Leri-Weill Dyschondrosteosis

About the Disease
Leri-Weill Dyschondrosteosis, also known as lwd, is related to madelung deformity and shox-related short stature. An important gene associated with Leri-Weill Dyschondrosteosis is SHOX (Short Stature Homeobox), and among its related pathways/superpathways is FGFR3 signaling in chondrocyte proliferation and terminal differentiation. Affiliated tissues include bone, skeletal muscle and eye, and related phenotypes are depressed nasal bridge and wide nasal bridge

Common Targets
SHOX | CYP26C1 | NPR2

Note: If you'd like to get a target analysis report for Leri-Weill Dyschondrosteosis, 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 Leri-Weill Dyschondrosteosis at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

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