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2009 ICD-9-CM
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| Mucopolysaccharidosis II Gargoylism, Hunter Syndrome | Hunter' | s Syndrome | Hunter Syndrome Gargoylism | Mucopolysaccharidosis 2 | Gargoylisms, Hunter Syndrome | Hunter Syndrome | Hunter Syndrome Gargoylisms | Hunters Syndrome | IIs, Mucopolysaccharidosis Systemic lysosomal storage disease marked by progressive physical deterioration and caused by a deficiency of L-sulfoiduronate sulfatase. This disease differs from MUCOPOLYSACCHARIDOSIS I by slower progression, lack of corneal clouding, and X-linked rather than autosomal recessive inheritance. The mild form produces near-normal intelligence and life span. The severe form usually causes death by age 15. |