Methylmalonic acidemia

MONDO:0002012

A genetically heterogenous inherited disorder characterized by abnormalities in the metabolism of lipids and proteins. Signs and symptoms usually appear early in life and vary from mild to life threatening. They include vomiting, dehydration, hypotonia, developmental delays, hepatomegaly, lethargy, intellectual disabilities, and chronic kidney disease.

Also known as: methylmalonic aciduria, METHYLMALONICACIDURIA due to methylmalonic CoA mutase deficiency, METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl A, METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl B, methylmalonic acidemia, cblA type, methylmalonic acidemia, cblB type, methylmalonic aciduria cblB type, methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency

31 clinical trials for this condition and its sub-types.

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