Medical dictionary. 2011.
3-Methylglutaconic aciduria — Classification and external resources 3 methylglutaconic acid DiseasesDB … Wikipedia
3-Methylglutaconic acid — Chembox new ImageFile = 3 methylglutaconic acid.svg ImageSize = IUPACName = (2E) 3 Methylpent 2 enedioic acid OtherNames = (E) 3 Methylglutaconic acid, 3 methyl 2 pentenedioic acid Section1 = Chembox Identifiers CASNo = 5746 90 7 PubChem = 99884… … Wikipedia
2-Hydroxyglutaric aciduria — Classification and external resources Alpha Hydroxyglutaric acid OMIM 600721 … Wikipedia
3 methylcrotonic aciduria — is a disorder characterised by urine that contains increased amounts of 3 methylcrotonic acid. It is caused by defects in a biotin dependent reaction that forms 3 methylglutaconic acid.External links* … Wikipedia
OPA3 — Optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) Identifiers Symbols OPA3; FLJ22187; FLJ25932; MGA3; MGC75494 External IDs … Wikipedia
Methylmalonic acidemia — Classification and external resources Methylmalonic acid ICD 10 E … 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
Inborn error of metabolism — Classification and external resources ICD 10 E70 E90 ICD 9 … Wikipedia
D-Glyceric acidemia — Classification and external resources OMIM 220120 D Glyceric Acidemia (a.k.a. D Glyceric Aciduria) is an inherited disease, in the category of inborn errors of metabolism. It is caused by a mutation in the gene GLYCTK, which encodes the for the… … Wikipedia
List of diseases (0-9) — The List of diseases starting with a non letter is part of the complete list of diseases. NOTOC *11 beta hydroxylase deficiency *10q Partial trisomy, rare (NIH) A rare disease (occurrence fewer than 1 case for 200,000) according to the public… … Wikipedia
