cataract-deafness-hypogonadism syndrome (Monarch Disease Ontology identifier MONDO_0015325) is an extremely rare multiple congenital abnormality syndrome, described in only three brothers to date, that is characterized by the association of congenital cataract, sensorineural deafness, hypogonadism, mild intellectual deficit, hypertrichosis, and short stature. There have been no further descriptions in the literature since 1995. Also known as: Schaap-Taylor-Baraitser syndrome.