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 - 4 of 4 for Hyperammonemia
  1. SLC25A15 gene 
    ... a human ORNT1 mutation (T32R) in the hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome. Pediatr Res. 2006 Oct;60( ... a defective ORNT1 in patients with the hyperornithinemia-hyperammonemia-homocitrullinuria syndrome, a urea cycle disorder. Mol Genet ...
    https://medlineplus.gov/genetics/gene/slc25a15 - Genetics
  2. CPT1A gene 
    ... hypoglycemia, increased levels of ammonia in the blood (hyperammonemia), and abnormalities in liver enzymes. A small percentage ...
    https://medlineplus.gov/genetics/gene/cpt1a - Genetics
  3. CA5A gene 
    ... VA deficiency resulting from CA5A alterations presents with hyperammonemia in early childhood. Am J Hum Genet. 2014 ...
    https://medlineplus.gov/genetics/gene/ca5a - Genetics
  4. NAGS gene 
    ... synthase gene associated with acute neonatal disease and hyperammonemia. Hum Genet. 2003 Apr;112(4):364-8. ...
    https://medlineplus.gov/genetics/gene/nags - Genetics