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Methylmalonicacidemia with homocystinuria, cbl D

Methylmalonicacidemia with homocystinuria, cbl D: Introduction

Methylmalonicacidemia with homocystinuria, cbl D: An inherited organic acid disorder where an enzyme deficiency (cblD) 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 Methylmalonicacidemia with homocystinuria, cbl D is available below.

Symptoms of Methylmalonicacidemia with homocystinuria, cbl D

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Wrongly Diagnosed with Methylmalonicacidemia with homocystinuria, cbl D?

Methylmalonicacidemia with homocystinuria, cbl D: Related Patient Stories

Causes of Methylmalonicacidemia with homocystinuria, cbl D

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Disease Topics Related To Methylmalonicacidemia with homocystinuria, cbl D

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