U.S. National Library of Medicine
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.
The numerical value of mucopolysaccharidosis ii in Chaldean Numerology is: 6
The numerical value of mucopolysaccharidosis ii in Pythagorean Numerology is: 5
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"mucopolysaccharidosis ii." Definitions.net. STANDS4 LLC, 2017. Web. 23 Nov. 2017. <http://www.definitions.net/definition/mucopolysaccharidosis ii>.