Orofaciodigital syndrome type 11 is an extremely rare, sporadic form of Orofaciodigital syndrome (OFDS; see this term) with only a few reported cases, and characterized by facial (blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures and low set ears) and skeletal (post-axial polydactyly and fusion of vertebrae) malformations along with severe intellectual disability, deafness and congenital heart defects. The disease is Orphanet_141000 (Orofaciodigital syndrome type 11). Also known as: OFD11, Oral-facial-digital syndrome type 11, Oral-facial-digital syndrome, Gabrielli type, Orofaciodigital syndrome, Gabrielli type.