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
See full list of 8
symptoms of Beta-mannosidosis
Wrongly Diagnosed with Beta-mannosidosis?
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
Read more about symptoms of Beta-mannosidosis
Statistics for Beta-mannosidosis
Beta-mannosidosis: Broader Related Topics
Types of Beta-mannosidosis
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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
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