Also Known As
Methylmalonic aciduria, vitamin B12-responsive, cblA typecobalamin A diseasecobalamin B diseasemethylmalonic acidemia cblA typemethylmalonic acidemia, cblA typemethylmalonic aciduria cblA typemethylmalonic aciduria, cblA typemethylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A typemethylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cblA typevitamin B12-responsive methylmalonic acidemia type cblAvitamin B12-responsive methylmalonic aciduria type cblAMMA Cbl A typecblA - cobalamin locus acblA methylmalonic acidemiacblB - cobalamin locus bcblB methylmalonic acidemiacobalamin locus A variantcobalamin locus B variantmethylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA complementation typemethylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type
Definition
An autosomal recessive form of methylmalonic aciduria, caused by mutation(s) in the MMAA gene, encoding MMAA protein.