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Mannosidosis, alpha B lysosomal

Mannosidosis, alpha B lysosomal: Introduction

Mannosidosis, alpha B lysosomal: A rare inherited metabolic disorder involving a deficiency of an enzyme (alpha-mannosidosase) which results in the accumulation of certain chemicals in the body which leads to progressive damage. More detailed information about the symptoms, causes, and treatments of Mannosidosis, alpha B lysosomal is available below.

Symptoms of Mannosidosis, alpha B lysosomal

Causes of Mannosidosis, alpha B lysosomal

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Definitions of Mannosidosis, alpha B lysosomal:

Mannosidosis, alpha B lysosomal is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Mannosidosis, alpha B lysosomal, or a subtype of Mannosidosis, alpha B lysosomal, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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More information about Mannosidosis, alpha B lysosomal

  1. Mannosidosis, alpha B lysosomal: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
 

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