CDH3 (Cadherin 3) is a Protein Coding gene. Diseases associated with CDH3 include Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy and Hypotrichosis, Congenital, With Juvenile Macular Dystrophy. Among its related pathways are Overview of nanoparticle effects and CDK-mediated phosphorylation and removal of Cdc6.