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Beta-mannosidosis

Beta-mannosidosis: Introduction

Beta-mannosidosis: A very rare type of inherited glycoprotein storage disease where deficiency of an enzyme called beta-mannosidase results in a build-up of certain sugars (oligosaccharides) which can harm the body. More detailed information about the symptoms, causes, and treatments of Beta-mannosidosis is available below.

Symptoms of Beta-mannosidosis

Wrongly Diagnosed with Beta-mannosidosis?

Beta-mannosidosis: Deaths

Read more about Deaths and Beta-mannosidosis.

Causes of Beta-mannosidosis

Read more about causes of Beta-mannosidosis.

Disease Topics Related To Beta-mannosidosis

Research the causes of these diseases that are similar to, or related to, Beta-mannosidosis:

Less Common Symptoms of Beta-mannosidosis

Statistics for Beta-mannosidosis

Beta-mannosidosis: Broader Related Topics

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Definitions of Beta-mannosidosis:

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

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

Related Beta-mannosidosis Info

Videos about Beta-mannosidosis

 

More information about Beta-mannosidosis

  1. Beta-mannosidosis: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths
 

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