Cleidocranial Dysplasia

About the Disease
Cleidocranial Dysplasia, also known as cleidocranial dysostosis, is related to parietal foramina with cleidocranial dysplasia and bone disease. An important gene associated with Cleidocranial Dysplasia is RUNX2 (RUNX Family Transcription Factor 2), and among its related pathways/superpathways are Signal Transduction and Endometrial cancer. Affiliated tissues include clavicle, skull and bone, and related phenotypes are frontal bossing and skeletal dysplasia

Common Targets
PKD1 | VAC14 | COL10A1 | FIG4 | RUNX2

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

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