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Results 1 - 10 of 48 for Acidemia
  1. 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 ...
  2. Methylmalonic acidemia with homocystinuria is a disorder in which the body is unable to correctly process certain protein building blocks (amino acids), fat building ...
  3. 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 ...
  4. 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 ...
  5. 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 ...
  6. 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 ...
  7. 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.
  8. ... CMAMMA Genetic Testing Registry: Combined malonic and methylmalonic acidemia Combined malonic and methylmalonic acidemia National Organization for Rare Disorders (NORD) ClinicalTrials.gov ...
  9. ... of glutathione synthase Deficiency of glutathione synthetase Pyroglutamic acidemia Pyroglutamic aciduria Genetic Testing Registry: Glutathione synthetase deficiency ...
  10. ... symptoms of the condition. Argininosuccinate lyase deficiency Argininosuccinic acidemia Argininosuccinicaciduria Argininosuccinyl-CoA lyase deficiency Arginosuccinase deficiency ASA ...
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