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- Glycine_encephalopathy abstract "Glycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism. The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism. There are several forms of the disease, with varying severity of symptoms and time of onset. The symptoms are exclusively neurological in nature, and clinically this disorder is characterized by abnormally high levels of the amino acid glycine in bodily fluids and tissues, especially the cerebral spinal fluid. Glycine encephalopathy is sometimes referred to as "nonketotic hyperglycinemia" (NKH), as a reference to the biochemical findings seen in patients with the disorder, and to distinguish it from the disorders that cause "ketotic hyperglycinemia" (seen in propionic acidemia and several other inherited metabolic disorders). To avoid confusion, the term "glycine encephalopathy" is often used, as this term more accurately describes the clinical symptoms of the disorder.".
- Glycine_encephalopathy meshId "D020158".
- Glycine_encephalopathy omim "605899".
- Glycine_encephalopathy thumbnail Glycin_-_Glycine.svg?width=300.
- Glycine_encephalopathy wikiPageExternalLink www.nkh-network.org.
- Glycine_encephalopathy wikiPageExternalLink 70.
- Glycine_encephalopathy wikiPageID "4003388".
- Glycine_encephalopathy wikiPageRevisionID "526346132".
- Glycine_encephalopathy caption Glycine.
- Glycine_encephalopathy hasPhotoCollection Glycine_encephalopathy.
- Glycine_encephalopathy meshid "D020158".
- Glycine_encephalopathy name "Glycine Encephalopathy".
- Glycine_encephalopathy omim "605899".
- Glycine_encephalopathy subject Category:Amino_acid_metabolism_disorders.
- Glycine_encephalopathy subject Category:Autosomal_recessive_disorders.
- Glycine_encephalopathy subject Category:Inborn_errors_of_metabolism.
- Glycine_encephalopathy type Abstraction100002137.
- Glycine_encephalopathy type Act100030358.
- Glycine_encephalopathy type AminoAcidMetabolismDisorders.
- Glycine_encephalopathy type Attribute100024264.
- Glycine_encephalopathy type AutosomalRecessiveDisorders.
- Glycine_encephalopathy type Condition113920835.
- Glycine_encephalopathy type Disease114070360.
- Glycine_encephalopathy type Disorder114052403.
- Glycine_encephalopathy type Event100029378.
- Glycine_encephalopathy type IllHealth114052046.
- Glycine_encephalopathy type Illness114061805.
- Glycine_encephalopathy type InbornErrorsOfMetabolism.
- Glycine_encephalopathy type Mistake100070965.
- Glycine_encephalopathy type Nonaccomplishment100066216.
- Glycine_encephalopathy type PathologicalState114051917.
- Glycine_encephalopathy type PhysicalCondition114034177.
- Glycine_encephalopathy type PsychologicalFeature100023100.
- Glycine_encephalopathy type State100024720.
- Glycine_encephalopathy type YagoPermanentlyLocatedEntity.
- Glycine_encephalopathy type Disease.
- Glycine_encephalopathy type Situation.
- Glycine_encephalopathy comment "Glycine encephalopathy (also known as non-ketotic hyperglycinemia or NKH) is a rare autosomal recessive disorder of glycine metabolism. After phenylketonuria, glycine encephalopathy is the second most common disorder of amino acid metabolism. The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism. There are several forms of the disease, with varying severity of symptoms and time of onset.".
- Glycine_encephalopathy label "Glycine encephalopathy".
- Glycine_encephalopathy sameAs m.0bc0jz.
- Glycine_encephalopathy sameAs Q17155687.
- Glycine_encephalopathy sameAs Q17155687.
- Glycine_encephalopathy sameAs 462.
- Glycine_encephalopathy sameAs Glycine_encephalopathy.
- Glycine_encephalopathy wasDerivedFrom Glycine_encephalopathy?oldid=526346132.
- Glycine_encephalopathy depiction Glycin_-_Glycine.svg.
- Glycine_encephalopathy isPrimaryTopicOf Glycine_encephalopathy.
- Glycine_encephalopathy name "Glycine Encephalopathy (Non-ketotic Hyperglycinemia)".
