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PEPCK 1 deficiency

PEPCK 1 deficiency: Introduction

PEPCK 1 deficiency: A rare inherited disorder where deficiency of an enzyme (phosphoenolpyruvate carboxykinase-1) prevents fats and proteins being turned into glucose which causes various problems. In type 1, the enzyme deficiency occurs in the liquid part of the cells. More detailed information about the symptoms, causes, and treatments of PEPCK 1 deficiency is available below.

Symptoms of PEPCK 1 deficiency

Wrongly Diagnosed with PEPCK 1 deficiency?

PEPCK 1 deficiency: Deaths

Read more about Deaths and PEPCK 1 deficiency.

Causes of PEPCK 1 deficiency

Read more about causes of PEPCK 1 deficiency.

Disease Topics Related To PEPCK 1 deficiency

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Misdiagnosis and PEPCK 1 deficiency

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Statistics for PEPCK 1 deficiency

PEPCK 1 deficiency: Broader Related Topics

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Definitions of PEPCK 1 deficiency:

PEPCK 1 deficiency is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that PEPCK 1 deficiency, or a subtype of PEPCK 1 deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related PEPCK 1 deficiency Info

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More information about PEPCK 1 deficiency

  1. PEPCK 1 deficiency: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Deaths
 

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