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Results 1 - 10 of 10 for GLYCINE
  1. Arginine:glycine amidinotransferase deficiency 
    Arginine:glycine amidinotransferase deficiency is an inherited disorder that primarily affects the brain. People with this disorder have mild ... when they have a fever.Children with arginine:glycine amidinotransferase deficiency may not gain weight and grow ...
    https://medlineplus.gov/...nineglycine-amidinotransferase-deficiency - Genetics
  2. 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
  3. Hypermethioninemia 
    ... GNMT gene provides instructions for making the enzyme glycine N-methyltransferase. This enzyme starts the next step ... parent with the condition. Deficiency of methionine adenosyltransferase Glycine N-methyltransferase deficiency GNMT deficiency Hepatic methionine adenosyltransferase ...
    https://medlineplus.gov/genetics/condition/hypermethioninemia - Genetics
  4. Hereditary hyperekplexia 
    ... the response of neurons to a molecule called glycine. This molecule is an amino acid, which is a building block of proteins. Glycine also acts as a neurotransmitter, which is a ...
    https://medlineplus.gov/genetics/condition/hereditary-hyperekplexia - Genetics
  5. Multiple mitochondrial dysfunctions syndrome 
    ... also have high levels of a molecule called glycine (hyperglycinemia) or elevated levels of sugar (hyperglycemia) in ... is also critical to the function of the glycine cleavage system, a set of proteins that breaks ...
    https://medlineplus.gov/...tiple-mitochondrial-dysfunctions-syndrome - Genetics
  6. Distal hereditary motor neuropathy, type V 
    ... gene provides instructions for making an enzyme called glycine--tRNA ligase, which is involved in the production ... V. The mutations probably reduce the activity of glycine--tRNA ligase. A reduction in the activity of ...
    https://medlineplus.gov/...distal-hereditary-motor-neuropathy-type-v - Genetics
  7. Spondyloepimetaphyseal dysplasia, Strudwick type 
    ... G, Cole T, Chapman S, Pope FM. A glycine to aspartic acid substitution of COL2A1 in a ...
    https://medlineplus.gov/...loepimetaphyseal-dysplasia-strudwick-type - Genetics
  8. Weissenbacher-Zweymüller syndrome 
    ... Wiesbauer P, Spranger J, Ala-Kokko L. Heterozygous glycine substitution in the COL11A2 gene in the original ...
    https://medlineplus.gov/.../weissenbacher-zweymuller-syndrome - Genetics
  9. Guanidinoacetate methyltransferase deficiency 
    ... creatine from the protein building blocks (amino acids) glycine, arginine, and methionine. Specifically, guanidinoacetate methyltransferase controls the ...
    https://medlineplus.gov/...idinoacetate-methyltransferase-deficiency - Genetics
  10. Amish lethal microcephaly 
    ... acid) alanine is substituted for the amino acid glycine at position 177 of the SLC25A19 protein, written ...
    https://medlineplus.gov/genetics/condition/amish-lethal-microcephaly - Genetics