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Methylcobalamin deficiency, cbl E complementation type

Methylcobalamin deficiency, cbl E complementation type: Introduction

Methylcobalamin deficiency, cbl E complementation type: An inherited organic acid disorder where an enzyme deficiency (cbl E) impairs the body's ability to break down cobalamin in the diet. This results in a buildup of homocystine which results in harmful affects. More detailed information about the symptoms, causes, and treatments of Methylcobalamin deficiency, cbl E complementation type is available below.

Symptoms of Methylcobalamin deficiency, cbl E complementation type

Wrongly Diagnosed with Methylcobalamin deficiency, cbl E complementation type?

Methylcobalamin deficiency, cbl E complementation type: Related Patient Stories

Causes of Methylcobalamin deficiency, cbl E complementation type

Read more about causes of Methylcobalamin deficiency, cbl E complementation type.

Misdiagnosis and Methylcobalamin deficiency, cbl E complementation type

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Methylcobalamin deficiency, cbl E complementation type: Broader Related Topics

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