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 - 10 of 11 for ARGININE OR CHOLINE OR LEVOCARNITINE OR ORNITHINE OR PANTOTHENIC ACID
Did you mean ARGININE OR CHOLINE OR "levo carnitine" OR ORNITHINE OR PANTOTHENIC ACID?
  1. Gyrate atrophy of the choroid and retina 
    ... retina OAT deficiency OKT deficiency Ornithine aminotransferase deficiency Ornithine keto acid aminotransferase deficiency Ornithine-delta-aminotransferase deficiency Ornithinemia with ...
    https://medlineplus.gov/.../gyrate-atrophy-of-the-choroid-and-retina - Genetics
  2. Caffey disease 
    ... Caffey disease replaces the protein building block (amino acid) arginine with the amino acid cysteine at protein position 836 (written as Arg836Cys ...
    https://medlineplus.gov/genetics/condition/caffey-disease - Genetics
  3. Arginine:glycine amidinotransferase deficiency 
    ... and hydrogen atoms called a guanidino group from arginine to glycine. Guanidinoacetic acid is converted to creatine in the second step of the process. Creatine is needed for the body to store and use energy properly.GATM ... amidinotransferase enzyme to participate in creatine synthesis, ...
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency - Genetics
  4. Glutaric acidemia type I 
    ... Burgard P. Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade ... efficacy and physiological actions of a lysine-free, arginine-rich formula to ... focus on cerebral amino acid influx. Mol Genet Metab. 2011 Sep-Oct;104( ...
    https://medlineplus.gov/genetics/condition/glutaric-acidemia-type-i - Genetics
  5. Lysinuric protein intolerance 
    ... protein disrupt the transportation of lysine, arginine, and ornithine. As a result, these amino acids are not absorbed by cells in the small ... leading to a shortage of lysine, arginine, and ornithine in the body. In the kidneys, the amino acids cannot be returned to the bloodstream (a process ...
    https://medlineplus.gov/.../condition/lysinuric-protein-intolerance - Genetics
  6. Arginase deficiency 
    ... is an inherited disorder that causes the amino acid arginine (a building block of proteins) and ammonia to ...
    https://medlineplus.gov/genetics/condition/arginase-deficiency - Genetics
  7. Argininosuccinic aciduria 
    ... to start the reaction in which the amino acid arginine, a building block of proteins, is produced from ...
    https://medlineplus.gov/genetics/condition/argininosuccinic-aciduria - Genetics
  8. Spondyloepiphyseal dysplasia with metatarsal shortening 
    ... metatarsal shortening replaces one protein building block (amino acid) known as arginine in the COL2A1 protein with another amino acid known as cysteine. This interferes with the assembly ...
    https://medlineplus.gov/...seal-dysplasia-with-metatarsal-shortening - Genetics
  9. Guanidinoacetate methyltransferase deficiency 
    ... compound creatine from the protein building blocks (amino acids) glycine, arginine, and methionine. Specifically, guanidinoacetate methyltransferase controls the second ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
  10. Miller syndrome 
    ... Citation on PubMed Brosnan ME, Brosnan JT. Orotic acid excretion and arginine metabolism. J Nutr. 2007 Jun;137(6 Suppl ...
    https://medlineplus.gov/genetics/condition/miller-syndrome - Genetics
previous · 1 · 2 · next