_:vb50939296 . . _:vb50939296 . . "A methylmalonic acidemia characterized by autosomal recessive inheritance, defects in the synthesis of AdoCbl, vitamin B12 therapy responsiveness and that has_material_basis_in homozygous or compound heterozygous mutation in the MMAB gene on chromosome 12q24."^^ . _:vb50939296 . "methylmalonic acidemia cblB type"^^ . "ORDO:79311"^^ . "OMIM:251110"^^ . "disease_ontology"^^ . "ICD10CM:E71.1"^^ . _:vb50939296 . . "methylmalonic aciduria cblB type"@en . "DOID:0060743"^^ . _:vb50939296 . "methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type"@en .