Robinow syndrome (RS) is a rare genetic syndrome characterized by limb shortening and abnormalities of the head, face and external genitalia. The disease is MONDO_0019978 (Robinow syndrome). Also known as: Robinow dwarfism, Robinow-Silverman-Smith syndrome, acral dysostosis with facial and genital abnormalities, fetal face syndrome, foetal face syndrome, mesomelic dwarfism-small genitalia syndrome.