MONDO_0009983 (retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome) can be described as follows. Retinitis pigmentosa - intellectual disability - deafness - hypogenitalism is an extremely rare syndromic retinitis pigmentosa characterized by pigmentary retinopathy, diabetes mellitus with hyperinsulinism, acanthosis nigricans, secondary cataracts, neurogenic deafness, short stature mild hypogonadism in males and polycystic ovaries with oligomenorrhea in females. Inheritance is thought to be autosomal recessive. It can be distinguished from Alstrom syndrome by the presence of intellectual disability and the absence of renal insufficiency. There have been no further descriptions in the literature since 1993. Also known as: retinitis pigmentosa-intellectual disability- labyrinthine deafness-hypogenitalism syndrome, retinitis pigmentosa-intellectual disability-sensorineural hearing loss-hypogenitalism syndrome.