Cleft lip/palate-deafness-sacral lipoma syndrome is characterized by cleft lip/palate, profound sensorineural deafness, and a sacral lipoma. It has been described in two brothers of Chinese origin born to non consanguineous parents. Additional findings included appendages on the heel and thigh, or anterior sacral meningocele and dislocated hip. The mode of inheritance is probably autosomal or X-linked recessive. The disease is cleft lip/palate-deafness-sacral lipoma syndrome (Monarch Disease Ontology entry MONDO_0016059). Also known as: Lowry-Yong syndrome.