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Aminotransferase
- GABA-transaminase deficiency is a brain disease (encephalopathy) that begins in infancy. Babies with this disorder have recurrent seizures (epilepsy), uncontrolled ...
- The AGXT gene provides instructions for making an enzyme called alanine-glyoxylate aminotransferase. This enzyme is found in liver cells, specifically within ...
- ... ABAT gene provides instructions for making the GABA-transaminase enzyme. This enzyme helps break down a brain ...
- ... gene provides instructions for making the enzyme ornithine aminotransferase. This enzyme is active in the energy-producing ... needed for the body's functions. The ornithine aminotransferase enzyme helps convert ornithine into another molecule called ...
- ... instructions for making a liver enzyme called tyrosine aminotransferase. This enzyme is the first in a series ... building block found in many foods. Specifically, tyrosine aminotransferase converts tyrosine into a byproduct called 4-hydroxyphenylpyruvate. ...
- ... gene provides instructions for making the enzyme ornithine aminotransferase. This enzyme is active in the energy-producing ... needed for the body's functions. The ornithine aminotransferase enzyme helps convert ornithine into another molecule called ...
- ... enzyme produced from the TAT gene, called tyrosine aminotransferase enzyme, is involved in the first step in ...
- ... Hyperoxaluria, primary Oxalosis Oxaluria, primary Peroxisomal alanine:glyoxylate aminotransferase deficiency Primary oxalosis Primary oxaluria Genetic Testing Registry: ...
- NGLY1-congenital disorder of deglycosylation (NGLY1-CDDG) is an inherited condition that affects many parts of the body. The severity of the signs and symptoms ...