Interestingly, autosomal dominantly inherited WNT5A dysfunction also results in right-ventricular outflow tract obstruction and renal anomalies with incomplete penetrance in addition to skeletal dysplasia features [Robinow syndrome; Online Mendelian Inheritance in Man (OMIM) #180700)] (Person et al., 2010). The gene discussed is WNT5A; the disease is skeletal dysplasia.