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Dicarboxylicaminoaciduria

Dicarboxylicaminoaciduria: Introduction

Dicarboxylicaminoaciduria: A rare metabolic syndrome involving a defect in the transport of certain amino acids (glutamate, aspartate) and resulting in high levels of dicarboxylic amino acids in the urine. Often no observable symptoms occur. More detailed information about the symptoms, causes, and treatments of Dicarboxylicaminoaciduria is available below.

Symptoms of Dicarboxylicaminoaciduria

Home Diagnostic Testing

Home medical testing related to Dicarboxylicaminoaciduria:

Wrongly Diagnosed with Dicarboxylicaminoaciduria?

Causes of Dicarboxylicaminoaciduria

Read more about causes of Dicarboxylicaminoaciduria.

Less Common Symptoms of Dicarboxylicaminoaciduria

Dicarboxylicaminoaciduria: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Dicarboxylicaminoaciduria

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Dicarboxylicaminoaciduria: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Statistics for Dicarboxylicaminoaciduria

Dicarboxylicaminoaciduria: Broader Related Topics

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Definitions of Dicarboxylicaminoaciduria:

Dicarboxylicaminoaciduria is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Dicarboxylicaminoaciduria, or a subtype of Dicarboxylicaminoaciduria, 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 Dicarboxylicaminoaciduria as a "rare disease".
Source - Orphanet

Related Dicarboxylicaminoaciduria Info

Videos about Dicarboxylicaminoaciduria

 

More information about Dicarboxylicaminoaciduria

  1. Dicarboxylicaminoaciduria: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
 

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