Aplasia Cutis Congenita

About the Disease
Aplasia Cutis Congenita, Nonsyndromic, also known as congenital defect of skull and scalp, is related to corpus callosum, agenesis of and aplasia cutis congenita. An important gene associated with Aplasia Cutis Congenita, Nonsyndromic is BMS1 (BMS1 Ribosome Biogenesis Factor). Affiliated tissues include skin, bone and brain, and related phenotypes are failure to thrive and hip dysplasia

Common Targets
FGF3 | DOCK6 | TP63 | ANGPTL8 | EDAR | G3845 | BMS1 | GJB6 | WNT10A | KCTD1 | DLL4 | KREMEN1 | RBPJ | EOGT

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

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