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What is Mannosidosis, alpha B lysosomal?

What is Mannosidosis, alpha B lysosomal?

  • 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.

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)

Mannosidosis, alpha B lysosomal: Introduction

Types of Mannosidosis, alpha B lysosomal:

Broader types of Mannosidosis, alpha B lysosomal:

What causes Mannosidosis, alpha B lysosomal?

Causes of Mannosidosis, alpha B lysosomal: see causes of Mannosidosis, alpha B lysosomal

What are the symptoms of Mannosidosis, alpha B lysosomal?

Symptoms of Mannosidosis, alpha B lysosomal: see symptoms of Mannosidosis, alpha B lysosomal

How is it treated?

Doctors and Medical Specialists for Mannosidosis, alpha B lysosomal: Medical Geneticist ; see also doctors and medical specialists for Mannosidosis, alpha B lysosomal.
Treatments for Mannosidosis, alpha B lysosomal: see treatments for Mannosidosis, alpha B lysosomal

Name and Aliases of Mannosidosis, alpha B lysosomal

Main name of condition: Mannosidosis, alpha B lysosomal

Other names or spellings for Mannosidosis, alpha B lysosomal:

Lysosomal alpha-D-mannosidase deficiency, Alpha mannosidosis, Alpha mannosidase B deficiency, Alpha mannosidosis type 1

Alpha mannosidase B deficiency, Alpha mannosidosis, Lysosomal Alpha-D-Mannosidase deficiency
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Mannosidosis, alpha B lysosomal: Related Conditions

Research the causes of these diseases that are similar to, or related to, Mannosidosis, alpha B lysosomal:

 

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