Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 5 of 5 for Aminotransferase
  1. GABA-transaminase deficiency 
    GABA-transaminase deficiency is a brain disease (encephalopathy) that begins in infancy. Babies with this disorder have recurrent seizures (epilepsy), uncontrolled ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  2. Gyrate atrophy of the choroid and retina 
    ... 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 ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  3. Tyrosinemia 
    ... enzyme produced from the TAT gene, called tyrosine aminotransferase enzyme, is involved in the first step in ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
  4. Primary hyperoxaluria 
    ... Hyperoxaluria, primary Oxalosis Oxaluria, primary Peroxisomal alanine:glyoxylate aminotransferase deficiency Primary oxalosis Primary oxaluria Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/primary-hyperoxaluria - Genetics
  5. NGLY1-congenital disorder of deglycosylation 
    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 ...
    https://medlineplus.gov/...y1-congenital-disorder-of-deglycosylation - Genetics