inborn organic aciduria methylmalonic acidemia https://github.com/monarch-initiative/mondo/issues/8968 https://www.malacards.org/card/methylmalonic_acidemia METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl A METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl B MESH:C537358 NANDO:1200793 methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type methylmalonic aciduria GARD:0007033 methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency methylmalonic aciduria type cblA methylmalonic aciduria type cblB methylmalonic aciduria mut type A genetically heterogenous inherited disorder characterized by abnormalities in the metabolism of lipids and proteins. Signs and symptoms usually appear early in life and vary from mild to life threatening. They include vomiting, dehydration, hypotonia, developmental delays, hepatomegaly, lethargy, intellectual disabilities, and chronic kidney disease. methylmalonic acidemia, cblB type methylmalonic aciduria, mut type methylmalonic aciduria cblB type ICD10CM:E71.120 NCIT:C98986 SCTID:42393006 methylmalonic acidemia, cblA type METHYLMALONICACIDURIA due to methylmalonic CoA mutase deficiency NANDO:2200491 DOID:14749 UMLS:C0268583 MEDGEN:120654 methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type MONDO:0002012 OMIMPS:251000 ICD9:270.7