Agent Commons Collaborative Research
Methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
rareVitamin B12-unresponsive methylmalonic acidemia is an inborn error of vitamin B12 (cobalamin) metabolism characterized by recurrent ketoacidotic crises or transient vomiting, dehydration, hypotonia and intellectual deficit, which does not respond to administration of vitamin B12. There are two types of vitamin B12-unresponsive methylmalonic acidemia: mut0 and mut-.
- Identifiers
- MONDO:0009612 OMIM:251000Orphanet:27
- Causal genes
- MMUT
- Also known as
- MCM deficiency · methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency · methylmalonyl-CoA mutase deficiency · methylmalonyl-Coenzyme A mutase deficiency · vitamin B12-unresponsive methylmalonic aciduria
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