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mucopolysaccharidosis type iiib

Medical Definition

A rare autosomal recessive lysosomal storage disease caused by deficiency of the enzyme n-acetyl-alpha-d-glucosaminidase. 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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