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Methylmalonic aciduria
Did you mean Methylmalonic acidemia?
- Combined malonic and methylmalonic aciduria (CMAMMA) is a condition characterized by high levels of certain chemicals, known as malonic acid and methylmalonic acid, in ...
- ... More About This Health Condition C2orf25 cblD CL25022 methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria methylmalonic aciduria ...
- ... of the condition. Fatal infantile lactic acidosis with methylmalonic aciduria Mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria) MTDPS9 Succinate-coenzyme A ligase deficiency SUCLG1 deficiency ...
- ... DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Mitochondrial DNA depletion syndrome, encephalomyopathic form with or ...
- ... methylmalonic acidemia. More About This Health Condition cblA methylmalonic aciduria (cobalamin deficiency) cblA type methylmalonic aciduria (cobalamin deficiency) ...
- ... Methylmalonic acidemia and homocystinemia Methylmalonic acidemia and homocystinuria Methylmalonic aciduria and homocystinuria Vitamin B12 metabolic defect with combined ...
- ... Adenosyltransferase ATR cblB CFAP23 cob(I)alamin adenosyltransferase methylmalonic aciduria (cobalamin deficiency) cblB type methylmalonic aciduria (cobalamin deficiency) ...
- ... homocystinuria. More About This Health Condition cblC DKFZP564I122 methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria ...
- ... and symptoms of the condition. Isolated methylmalonic acidemia Methylmalonic aciduria MMA Genetic Testing Registry: Methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency Genetic Testing Registry: Methylmalonic aciduria, cblA type Genetic Testing Registry: Methylmalonic aciduria, cblB ...
- ... been found in people with combined malonic and methylmalonic aciduria (CMAMMA), a condition characterized by elevated levels of ... J, Rosenblatt DS, Braverman N. Combined malonic and methylmalonic aciduria: exome sequencing reveals mutations in the ACSF3 gene ...