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PEPCK 2 deficiency

PEPCK 2 deficiency: Introduction

PEPCK 2 deficiency: A rare inherited disorder where deficiency of an enzyme (phosphoenolpyruvate carboxykinase-2) prevents fats and proteins being turned into glucose which causes various problems. In type 2 the deficiency occurs in the mitochondrial part of the cell which is the energy conversion organelle in the cell. More detailed information about the symptoms, causes, and treatments of PEPCK 2 deficiency is available below.

Symptoms of PEPCK 2 deficiency

Wrongly Diagnosed with PEPCK 2 deficiency?

PEPCK 2 deficiency: Deaths

Read more about Deaths and PEPCK 2 deficiency.

Causes of PEPCK 2 deficiency

Read more about causes of PEPCK 2 deficiency.

Disease Topics Related To PEPCK 2 deficiency

Research the causes of these diseases that are similar to, or related to, PEPCK 2 deficiency:

Misdiagnosis and PEPCK 2 deficiency

Vitamin B12 deficiency under-diagnosed: The condition of Vitamin B12 deficiency is a possible misdiagnosis of various conditions, such as multiple sclerosis (see symptoms of multiple sclerosis). See more »

Statistics for PEPCK 2 deficiency

PEPCK 2 deficiency: Broader Related Topics

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Definitions of PEPCK 2 deficiency:

PEPCK 2 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 2 deficiency, or a subtype of PEPCK 2 deficiency, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Related PEPCK 2 deficiency Info

Videos about PEPCK 2 deficiency


More information about PEPCK 2 deficiency

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

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