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What is Methylcobalamin deficiency cbl G type?

What is Methylcobalamin deficiency cbl G type?

  • Methylcobalamin deficiency cbl G type: An inherited organic acid disorder where an enzyme deficiency (cbl G) impairs the body's ability to break down certain proteins consumed in the diet. This results in a buildup of homocystine which results in harmful affects.

Methylcobalamin deficiency cbl G type: Introduction

Types of Methylcobalamin deficiency cbl G type:

Broader types of Methylcobalamin deficiency cbl G type:

What causes Methylcobalamin deficiency cbl G type?

Causes of Methylcobalamin deficiency cbl G type: see causes of Methylcobalamin deficiency cbl G type

What are the symptoms of Methylcobalamin deficiency cbl G type?

Symptoms of Methylcobalamin deficiency cbl G type: see symptoms of Methylcobalamin deficiency cbl G type

Methylcobalamin deficiency cbl G type: Testing

Misdiagnosis: see misdiagnosis and Methylcobalamin deficiency cbl G type.

How is it treated?

Doctors and Medical Specialists for Methylcobalamin deficiency cbl G type: Medical Geneticist ; see also doctors and medical specialists for Methylcobalamin deficiency cbl G type.
Treatments for Methylcobalamin deficiency cbl G type: see treatments for Methylcobalamin deficiency cbl G type

Name and Aliases of Methylcobalamin deficiency cbl G type

Main name of condition: Methylcobalamin deficiency cbl G type

Other names or spellings for Methylcobalamin deficiency cbl G type:

homocystinuria-megaloblastic anemia due to defect in cobalamin metabolism, cblG complementation type

 

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