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Methylmalonicaciduria with homocystinuria, cobalamin F

Methylmalonicaciduria with homocystinuria, cobalamin F: Introduction

Methylmalonicaciduria with homocystinuria, cobalamin F: An inherited organic acid disorder where an enzyme deficiency (cbl F) impairs the body's ability to break down certain proteins (methionine, threonine, isoleucine and valine) consumed in the diet. This results in a buildup of methylmalonic acid and homocystine which results in harmful affects. More detailed information about the symptoms, causes, and treatments of Methylmalonicaciduria with homocystinuria, cobalamin F is available below.

Symptoms of Methylmalonicaciduria with homocystinuria, cobalamin F

Wrongly Diagnosed with Methylmalonicaciduria with homocystinuria, cobalamin F?

Methylmalonicaciduria with homocystinuria, cobalamin F: Related Patient Stories

Methylmalonicaciduria with homocystinuria, cobalamin F: Complications

Review possible medical complications related to Methylmalonicaciduria with homocystinuria, cobalamin F:

Causes of Methylmalonicaciduria with homocystinuria, cobalamin F

Read more about causes of Methylmalonicaciduria with homocystinuria, cobalamin F.

Disease Topics Related To Methylmalonicaciduria with homocystinuria, cobalamin F

Research the causes of these diseases that are similar to, or related to, Methylmalonicaciduria with homocystinuria, cobalamin F:

Methylmalonicaciduria with homocystinuria, cobalamin F: Broader Related Topics

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More information about Methylmalonicaciduria with homocystinuria, cobalamin F

  1. Methylmalonicaciduria with homocystinuria, cobalamin F: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Complications
 

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