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mucopolysaccharidosis type iiid

Medical Definition

A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme n-acetylglucosamine-6-sulfatase. it is characterized by behavioral changes, sleep disturbances and mental developmental delays.
Related Codes (1)
Code
Description
Billable
Details
E76.22Sanfilippo mucopolysaccharidoses

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