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.
See full list of 23 symptoms of Methylmalonicaciduria with homocystinuria, cobalamin F
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