Orphanet rare-disease nomenclature id Orphanet_2751 (Orofaciodigital syndrome type 2) can be described as follows. Oral-facial-digital (OFD) type 2 is characterized by hand and feet deformities, facial deformities, midline cleft of the upper lip and tongue hamartomas. Also known as: Mohr syndrome, OFD2, Oral-facial-digital syndrome type 2.