The disease is albinism. The most common form of albinism is caused by a deficiency of copper-dependent tyrosinase (tyrosine hydroxylase), blocking the production of melanin from the aromatic amino acid tyrosine. Affected individuals lack melanin pigment in skin, hair, and eyes, and are prone to develop sun-induced skin cancers, including both squamous cell carcinomas and melanomas. Maple syrup urine disease is an example of a disorder of branched chain amino acids causing motor abnormalities and seizures. Tay-Sachs disease is an example of a disorder of glycolipids. In this disorder, a deficiency of hexosaminidase A leads to accumulation of ganglioside GM2. Hunter's disease is an example of a disorder of glycoproteins. This mucopolysaccharidosis is inherited as an autosomal recessive trait. Ref: Murray R.K. (2011). Chapter 1. Biochemistry & Medicine. In D.A. Bender, K.M. Botham, P.A. Weil, P.J. Kennelly, R.K. Murray, V.W. Rodwell (Eds), Harper's Illustrated Biochemistry, 29e.