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bn:03112237n
Noun Concept
Categories: Phospholipid metabolism disorders
EN
3-methylglutaconic aciduria  3-methyl glutaconic aciduria  3-Methylglutaconic acidemia  3-Methylglutaconic aciduria type 1  3-Methylglutaconic aciduria type 3
EN
3-Methylglutaconic aciduria is any of at least five metabolic disorders that impair the body's ability to make energy in the mitochondria. Wikipedia
Definitions
Relations
Sources
EN
3-Methylglutaconic aciduria is any of at least five metabolic disorders that impair the body's ability to make energy in the mitochondria. Wikipedia
A metabolic disorder Wikipedia Disambiguation
Organic acidemia that is characterized by elevated levels of 3-methylglutaconic acid and 3-methylglutaric acid in the urine Wikidata
IS A
rare disease
organic acidemia
HAS KIND
Barth syndrome
3-methylglutaconic aciduria type 5
Costeff syndrome
3-methylglutaconic aciduria type 1
GENETIC ASSOCIATION
methylglutaconyl-CoA hydratase
NAMED AFTER
Barth
Wikipedia
EN
3-methylglutaconic aciduria
Wikidata
EN
3-methylglutaconic aciduria
Wikipedia Redirections
EN
3-methyl glutaconic aciduria, 3-Methylglutaconic acidemia, 3-methylglutaconic aciduria, 3-Methylglutaconic aciduria type 1, 3-Methylglutaconic aciduria type 3, 3-Methylglutaconic aciduria type 4, 3-Methylglutaconic aciduria type 5, 3-methylglutaconic aciduria type I, 3-methylglutaconic aciduria type III, 3-methylglutaconic aciduria type IV, 3-Methylglutaconic aciduria type V, 3-Methylglutaconyl-CoA Hydratase Deficiency, 3 methylglutaconyl coa hydratase deficiency, 3MGA, MGA type 1, MGA type 3, MGA type 4, MGA type 5, MGA type I, MGA type III, MGA type IV, MGA type V

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