A rare multiple congenital anomalies syndrome characterized by facial dysmorphism (hypertelorism, broad and high nasal bridge, depressed nasal ridge, short columella, underdeveloped maxilla, and prominent cupid-bow upper lip vermillion), mild to severe congenital sensorineural hearing loss, and skeletal abnormalities consisting of brachytelephalangy and broad thumbs and halluces with large, rounded epiphyses. Additional manifestations that have been reported include pulmonary valve stenosis, voice hoarseness and renal agenesis. The disease is Keipert syndrome (MONDO_0009720, a Monarch Disease Ontology id). Also known as: KPTS, Keipert syndrome, X-linked recessive, nasodigitoacoustic syndrome, nasodigitoacoustic syndrome, formerly.