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Acidemia
- Glutaric acidemia type I (also called glutaric aciduria type I) is an inherited disorder in which the body is unable to process certain proteins properly. It is ...
- Glutaric acidemia type II is an inherited disorder that interferes with the body's ability to break down proteins and fats to produce energy. Incompletely processed ...
- Methylmalonic acidemia with homocystinuria is a disorder in which the body is unable to correctly process certain protein building blocks (amino acids), fat building ...
- Propionic acidemia is an inherited disorder in which the body is unable to process certain parts of proteins and lipids (fats) properly. It is classified as an ...
- Isovaleric acidemia is a rare disorder in which the body is unable to properly break down a particular protein building block (amino acid). The condition is classified ...
- Methylmalonic acidemia is a group of inherited disorders that prevent the body from breaking down proteins and fats (lipids) properly. The effects of methylmalonic acidemia, which usually appear in early infancy, vary from ...
- Methylmalonic acidemia is a disorder in which the body cannot break down certain proteins and fats. The result is ... may die before it is ever diagnosed. Methylmalonic acidemia affects boys and girls equally.
- ... CMAMMA Genetic Testing Registry: Combined malonic and methylmalonic acidemia Combined malonic and methylmalonic acidemia National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
- ... of glutathione synthase Deficiency of glutathione synthetase Pyroglutamic acidemia Pyroglutamic aciduria Genetic Testing Registry: Glutathione synthetase deficiency ...
- ... symptoms of the condition. Argininosuccinate lyase deficiency Argininosuccinic acidemia Argininosuccinicaciduria Argininosuccinyl-CoA lyase deficiency Arginosuccinase deficiency ASA ...