Robinow Syndrome, Autosomal Dominant 2 (DRS2)

Robinow Syndrome, Autosomal Dominant 2, also known as autosomal dominant robinow syndrome 2, is related to omodysplasia 2 and omodysplasia 1. An important gene associated with Robinow Syndrome, Autosomal Dominant 2 is DVL1 (Dishevelled Segment Polarity Protein 1), and among its related pathways/superpathways are CTNNB1 S33 mutants aren't phosphorylated and Breast cancer pathway. Affiliated tissues include bone and heart, and related phenotypes are umbilical hernia and sensorineural hearing impairment