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methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Vitamin 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-.
Uniprot Description An often fatal disorder of organic acid metabolism. Common clinical features include lethargy, vomiting, failure to thrive, hypotonia, neurological deficit and early death. Two forms of the disease are distinguished by the presence (mut-) or absence (mut0) of residual enzyme activity. Mut0 patients have more severe neurological manifestations of the disease than do MUT- patients. MMAM is unresponsive to vitamin B12 therapy.
Mondo Term and Equivalent IDs
MONDO:0009612:  methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency
GARD:0003586: 
NCIT:C148366: 
Orphanet:27: 
UMLS:C1855114: