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Mucopolysaccharidosis, type 9

Mucopolysaccharidosis, type 9: Introduction

Mucopolysaccharidosis, type 9: A rare inherited biochemical disorder characterized by the accumulation of mucopolysaccharides (glycosaminoglycans) in various body tissues due to insufficient amounts of an enzyme (hyaluronidase) needed to break it down. More detailed information about the symptoms, causes, and treatments of Mucopolysaccharidosis, type 9 is available below.

Symptoms of Mucopolysaccharidosis, type 9

Causes of Mucopolysaccharidosis, type 9

Read more about causes of Mucopolysaccharidosis, type 9.

Statistics for Mucopolysaccharidosis, type 9

Mucopolysaccharidosis, type 9: Broader Related Topics

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Definitions of Mucopolysaccharidosis, type 9:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Mucopolysaccharidosis, type 9 as a "rare disease".
Source - Orphanet

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Videos about Mucopolysaccharidosis, type 9

 

More information about Mucopolysaccharidosis, type 9

  1. Mucopolysaccharidosis, type 9: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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