Autosomal Dominant Robinow Syndrome

Autosomal Dominant Robinow Syndrome, also known as robinow syndrome, autosomal dominant, is related to robinow syndrome, autosomal dominant 3 and robinow syndrome, autosomal dominant 1. An important gene associated with Autosomal Dominant Robinow Syndrome is WNT5A (Wnt Family Member 5A), and among its related pathways/superpathways are Signal Transduction and Nanog in Mammalian ESC Pluripotency. Affiliated tissues include bone and tongue, and related phenotypes are hypertelorism and wide nasal bridge