Cantu Syndrome

About the Disease
Cantu Syndrome, also known as hypertrichotic osteochondrodysplasia, is related to cardiomyopathy, dilated, 1o and patent ductus arteriosus 1. An important gene associated with Cantu Syndrome is ABCC9 (ATP Binding Cassette Subfamily C Member 9), and among its related pathways/superpathways are Transmission across Chemical Synapses and Potassium Channels. Affiliated tissues include bone, heart and skin, and related phenotypes are coarse facial features and thick vermilion border

Common Targets
ABCC9

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

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