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 91 for ALANINE OR ARGININE OR DEXTROSE OR GLYCINE OR HISTIDINE OR ISOLEUCINE OR LEUCINE OR LYSINE OR METHIONINE OR PHENYLALANINE OR PROLINE OR SERINE OR THREONINE OR TRYPTOPHAN OR TYROSINE OR VALINE
  1. Arginine:glycine amidinotransferase deficiency 
    Arginine:glycine amidinotransferase deficiency is an inherited disorder that primarily affects the brain. People with this disorder have mild to moderate intellectual ...
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency - Genetics
  2. Tyrosine hydroxylase deficiency 
    Tyrosine hydroxylase (TH) deficiency is a disorder that primarily affects movement. There are three forms of tyrosine hydroxylase deficiency, and they are categorized ...
    https://medlineplus.gov/.../tyrosine-hydroxylase-deficiency - Genetics
  3. Phenylketonuria 
    ... that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a protein building block (an amino acid) ... some artificial sweeteners. If PKU is not treated, phenylalanine can build up to harmful levels in the ...
    https://medlineplus.gov/genetics/condition/phenylketonuria - Genetics
  4. Hyperlysinemia 
    ... by elevated blood levels of the amino acid lysine, a building block of most proteins. Hyperlysinemia is ... shortage (deficiency) of the enzyme that breaks down lysine. Hyperlysinemia typically causes no health problems, and most ...
    https://medlineplus.gov/genetics/condition/hyperlysinemia - Genetics
  5. Tyrosinemia 
    ... characterized by problems breaking down the amino acid tyrosine, which is a building block of most proteins. If the condition is untreated, tyrosine and its byproducts build up in tissues and ...
    https://medlineplus.gov/genetics/condition/tyrosinemia - Genetics
  6. Hyperprolinemia 
    ... a particular protein building block (amino acid), called proline, in the blood. This condition generally occurs when proline is not broken down properly by the body. ...
    https://medlineplus.gov/genetics/condition/hyperprolinemia - Genetics
  7. Histidinemia 
    ... by elevated blood levels of the amino acid histidine, a building block of most proteins. Histidinemia is ... shortage (deficiency) of the enzyme that breaks down histidine. Histidinemia typically causes no health problems, and most ...
    https://medlineplus.gov/genetics/condition/histidinemia - Genetics
  8. Nonketotic hyperglycinemia 
    ... by abnormally high levels of a molecule called glycine in the body (hyperglycinemia). The excess glycine builds up in tissues and organs, particularly the ...
    https://medlineplus.gov/.../condition/nonketotic-hyperglycinemia - Genetics
  9. Phosphoglycerate dehydrogenase deficiency 
    ... production of the protein building block (amino acid) serine. Specifically, the enzyme converts a substance called 3- ... to 3-phosphohydroxypyruvate in the first step in serine production. Serine is necessary for the development and ...
    https://medlineplus.gov/...phosphoglycerate-dehydrogenase-deficiency - Genetics
  10. Beta-ureidopropionase deficiency 
    ... carbamyl-beta-aminoisobutyric acid and N-carbamyl-beta-alanine to be released in the urine. Neurological problems ... acid and also breaks down N-carbamyl-beta-alanine to beta-alanine, ammonia, and carbon dioxide. Both ...
    https://medlineplus.gov/.../beta-ureidopropionase-deficiency - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next