obsolete_Treacher-Collins syndrome true Tomasz Adamusiak use 'http://www.orpha.net/ORDO/Orphanet_861' instead. New Label : Treacher-Collins syndrome true Treacher Collins Syndrome 2.32 MESH:D008342 Mandibulofacial Dysostosis Syndrome, Treacher Collins Mandibulofacial Dysostoses Collins Syndrome, Treacher http://www.orpha.net/ORDO/Orphanet_861 Dysostoses, Mandibulofacial Dysostosis, Mandibulofacial OMIM:154500 A hereditary disorder occurring in two forms: the complete form (Franceschetti's syndrome) is characterized by antimongoloid slant of the palpebral fissures, coloboma of the lower lid, micrognathia and hypoplasia of the zygomatic arches, and microtia. It is transmitted as an autosomal trait. The incomplete form (Treacher Collins syndrome) is characterized by the same anomalies in less pronounced degree. It occurs sporadically, but an autosomal dominant mode of transmission is suspected. (Dorland, 27th ed)