A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by craniofacial dysmorphism (midface hypoplasia, depressed nasal bridge, small nose with upturned tip, cleft palate, Pierre Robin sequence), bilateral, pronounced sensorineural hearing loss, and skeletal/joint anomalies (including spondyloepiphyseal dysplasia, arthralgia/arthropathy), in the absence of ocular abnormalities. The disease is otospondylomegaepiphyseal dysplasia, autosomal dominant (MONDO_0008490). Also known as: COL11A2 Stickler syndrome, OSMED, Heterozygous, OSMED, heterozygous, OSMEDA, Piere-Robin syndrome, Pierre Robin malformation, Pierre Robin sequence-fetal chondrodysplasia syndrome, Pierre Robin syndrome with fetal chondrodysplasia.