Glutaric Acidemia

What is glutaric acidemia type I?
Glutaric acidemia type I is an inherited disorder in which the body is unable to process certain proteins properly.

Glutaric Acidemia Type II ... heart failure
Glutaric aciduria type II ... heart failure
Glutaric Aciduria, neonatal form of type II A ... heart failure
Glycogen debranching deficiency ... enlarged heart
Gonorrhea ... endocarditis ...

GA II
Glutaric Acidemia II
Glutaric Aciduria II
Glutaricacidemia II
Multiple Acyl-Co-A Dehydrogenation Deficiency
MADD
Electron Transfer Flavoprotein: Ubiquinone Oxidoreductase, Deficiency of
Electron Transfer Flavoprotein, Deficiency of ...

disorder (N-Acetylglutamate synthase deficiency, Carbamoyl phosphate synthetase I deficiency, Ornithine transcarbamylase deficiency/translocase deficiency, Citrullinemia, Argininosuccinic aciduria, Argininemia, Hyperammonemia) - Glutaric acidemia ...

Glutaric Acidemia I
Glutaric Acidemia II
Glutaric Aciduria I
Glutaric Aciduria II
Glutaricacidemia I
Glutaricacidemia II
Glutaricaciduria I
Glutaricaciduria II
Glutaryl-CoA Dehydrogenase Deficiency
GlutaSolve - Medication ...

Definitions:
1. A dicarboxylic acid that accumulates in people with glutaric acidemia type I.
The information shown above for 3-hydroxyglutaric acid is provided by Stedman's.

3-Hydroxy-3-methylglutaric aciduria (HMG)
3-Methylcrotonyl-CoA carboxylase deficiency (3MCC)
Beta ketothiolase deficiency
Glutaric acidemia type I
Isovaleric acidemia
Methylmalonic acidemia
Multiple carboxylase deficiency (MCD)
Propionic acidemia ...

See also: Deficiency, Glycogen Storage Disease, Malabsorption, Storage disease, Galactosemia