The new mediacal dictionary. 2014.
methylmalonic aciduria — Excretion of excessive amounts of methylmalonic acid in urine owing to deficient activity of methylmalonyl CoA mutase or deficient cobalamin reductase. Two types occur: 1) an inborn error of metabolism resulting in severe … Medical dictionary
methylmalonic acidaemia — methylmalonic aciduria … The new mediacal dictionary
Methylmalonic acidemia — Classification and external resources Methylmalonic acid ICD 10 E … Wikipedia
3-Methylglutaconic aciduria — Classification and external resources 3 methylglutaconic acid DiseasesDB … Wikipedia
2-Hydroxyglutaric aciduria — Classification and external resources Alpha Hydroxyglutaric acid OMIM 600721 … Wikipedia
Glutaric aciduria type 1 — DiseaseDisorder infobox Name = Glutaric acidemia type 1 ICD10 = ICD10|E|72|3|e|70 ICD9 = ICDO = Caption = Glutaric acid OMIM = 231670 MedlinePlus = eMedicineSubj = eMedicineTopic = DiseasesDB = 29830 Glutaric acidemia type 1 (or Glutaric Aciduria … Wikipedia
β-hydroxypropionic aciduria — Elevated levels of β hydroxypropionic acid in the urine; seen in defects in methylmalonic acid and propionate metabolism, as well as in ketotic hyperglycinemia syndrome … Medical dictionary
MMAB — Methylmalonic aciduria (cobalamin deficiency) cblB type, also known as MMAB, is a human gene.cite web | title = Entrez Gene: MMAB methylmalonic aciduria (cobalamin deficiency) cblB type| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… … Wikipedia
Methylmalonyl-CoA mutase — Rendering based on PDB 2XIJ … Wikipedia
Organic acidemia — Organic acidemia, also called organic aciduria, is a term used to classify a group of metabolic disorders which disrupt normal amino acid metabolism, particularly branched chain amino acids, causing a buildup of acids which are usually not… … Wikipedia
