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Results 1 - 10 of 21 for Methylmalonic aciduria
Did you mean Methylmalonic acidemia?
  1. Combined malonic and methylmalonic aciduria (CMAMMA) is a condition characterized by high levels of certain chemicals, known as malonic acid and methylmalonic acid, in ...
  2. ... More About This Health Condition C2orf25 cblD CL25022 methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria methylmalonic aciduria ...
  3. ... 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 ...
  4. ... DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria) Mitochondrial DNA depletion syndrome, encephalomyopathic form with or ...
  5. ... methylmalonic acidemia. More About This Health Condition cblA methylmalonic aciduria (cobalamin deficiency) cblA type methylmalonic aciduria (cobalamin deficiency) ...
  6. ... Methylmalonic acidemia and homocystinemia Methylmalonic acidemia and homocystinuria Methylmalonic aciduria and homocystinuria Vitamin B12 metabolic defect with combined ...
  7. ... Adenosyltransferase ATR cblB CFAP23 cob(I)alamin adenosyltransferase methylmalonic aciduria (cobalamin deficiency) cblB type methylmalonic aciduria (cobalamin deficiency) ...
  8. ... homocystinuria. More About This Health Condition cblC DKFZP564I122 methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria methylmalonic aciduria ...
  9. ... 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 ...
  10. ... 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 ...
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