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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 thumbnail Glycin_-_Glycine.svg?width=300.
- Glycine_encephalopathy wikiPageExternalLink glycine-encephalopathy.
- Glycine_encephalopathy wikiPageExternalLink www.nkh-network.org.
- Glycine_encephalopathy wikiPageExternalLink nonketotic-hyperglycinemia.
- Glycine_encephalopathy wikiPageID "4003388".
- Glycine_encephalopathy wikiPageLength "13074".
- Glycine_encephalopathy wikiPageOutDegree "58".
- Glycine_encephalopathy wikiPageRevisionID "669409551".
- Glycine_encephalopathy wikiPageWikiLink Amino_acid.
- Glycine_encephalopathy wikiPageWikiLink Aminomethyltransferase.
- Glycine_encephalopathy wikiPageWikiLink Ammonia.
- Glycine_encephalopathy wikiPageWikiLink Apnea.
- Glycine_encephalopathy wikiPageWikiLink Ataxia.
- Glycine_encephalopathy wikiPageWikiLink Autosomal_recessive.
- Glycine_encephalopathy wikiPageWikiLink Autosome.
- Glycine_encephalopathy wikiPageWikiLink Blood_plasma.
- Glycine_encephalopathy wikiPageWikiLink Carbon_dioxide.
- Glycine_encephalopathy wikiPageWikiLink Category:Amino_acid_metabolism_disorders.
- Glycine_encephalopathy wikiPageWikiLink Category:Autosomal_recessive_disorders.
- Glycine_encephalopathy wikiPageWikiLink Category:Inborn_errors_of_metabolism.
- Glycine_encephalopathy wikiPageWikiLink Cerebrospinal_fluid.
- Glycine_encephalopathy wikiPageWikiLink Chorea.
- Glycine_encephalopathy wikiPageWikiLink Cofactor_(biochemistry).
- Glycine_encephalopathy wikiPageWikiLink Congenital_disorders_of_amino_acid_metabolism.
- Glycine_encephalopathy wikiPageWikiLink Conjugate_gaze_palsy.
- Glycine_encephalopathy wikiPageWikiLink Dihydrolipoamide_dehydrogenase.
- Glycine_encephalopathy wikiPageWikiLink Dominance_(genetics).
- Glycine_encephalopathy wikiPageWikiLink Enzyme.
- Glycine_encephalopathy wikiPageWikiLink Epileptic_seizure.
- Glycine_encephalopathy wikiPageWikiLink Febrile.
- Glycine_encephalopathy wikiPageWikiLink Fever.
- Glycine_encephalopathy wikiPageWikiLink File:Autorecessive.svg.
- Glycine_encephalopathy wikiPageWikiLink GCSH.
- Glycine_encephalopathy wikiPageWikiLink GLDC.
- Glycine_encephalopathy wikiPageWikiLink Gaze_palsy.
- Glycine_encephalopathy wikiPageWikiLink Gene.
- Glycine_encephalopathy wikiPageWikiLink Genetic_carrier.
- Glycine_encephalopathy wikiPageWikiLink Glycine.
- Glycine_encephalopathy wikiPageWikiLink Glycine_cleavage_system.
- Glycine_encephalopathy wikiPageWikiLink Glycine_dehydrogenase_(decarboxylating).
- Glycine_encephalopathy wikiPageWikiLink Heterozygotes.
- Glycine_encephalopathy wikiPageWikiLink Hypotonia.
- Glycine_encephalopathy wikiPageWikiLink Inborn_error_of_metabolism.
- Glycine_encephalopathy wikiPageWikiLink Inborn_errors_of_metabolism.
- Glycine_encephalopathy wikiPageWikiLink Intellectual_disability.
- Glycine_encephalopathy wikiPageWikiLink Lethargy.
- Glycine_encephalopathy wikiPageWikiLink List_of_amino_acid_metabolism_disorders.
- Glycine_encephalopathy wikiPageWikiLink Mental_retardation.
- Glycine_encephalopathy wikiPageWikiLink Mitochondria.
- Glycine_encephalopathy wikiPageWikiLink Mitochondrion.
- Glycine_encephalopathy wikiPageWikiLink Movement_disorder.
- Glycine_encephalopathy wikiPageWikiLink Movement_disorders.
- Glycine_encephalopathy wikiPageWikiLink Multiprotein_complex.
- Glycine_encephalopathy wikiPageWikiLink Myoclonic_jerks.
- Glycine_encephalopathy wikiPageWikiLink Myoclonus.
- Glycine_encephalopathy wikiPageWikiLink Neurotransmitter.
- Glycine_encephalopathy wikiPageWikiLink Optic_atrophy.
- Glycine_encephalopathy wikiPageWikiLink Optic_neuropathy.
- Glycine_encephalopathy wikiPageWikiLink Organic_acidemia.
- Glycine_encephalopathy wikiPageWikiLink Organic_acidemias.
- Glycine_encephalopathy wikiPageWikiLink Phenylketonuria.
- Glycine_encephalopathy wikiPageWikiLink Propionic_acidemia.
- Glycine_encephalopathy wikiPageWikiLink Protein_complex.
- Glycine_encephalopathy wikiPageWikiLink Recessive_gene.
- Glycine_encephalopathy wikiPageWikiLink Seizures.
- Glycine_encephalopathy wikiPageWikiLink Spastic_diplegia.
- Glycine_encephalopathy wikiPageWikiLink Stereoisomerism.
- Glycine_encephalopathy wikiPageWikiLink Stereoisomers.
- Glycine_encephalopathy wikiPageWikiLink Valproate.
- Glycine_encephalopathy wikiPageWikiLink Valproic_acid.
- Glycine_encephalopathy wikiPageWikiLink Zygosity.
- Glycine_encephalopathy wikiPageWikiLinkText "Glycine encephalopathy".
- Glycine_encephalopathy wikiPageWikiLinkText "glycine encephalopathy".
- Glycine_encephalopathy caption Glycine.
- Glycine_encephalopathy hasPhotoCollection Glycine_encephalopathy.
- Glycine_encephalopathy meshid "D020158".
- Glycine_encephalopathy name "Glycine Encephalopathy".
- Glycine_encephalopathy omim "605899".
- Glycine_encephalopathy wikiPageUsesTemplate Template:Amino_acid_metabolic_pathology.
- Glycine_encephalopathy wikiPageUsesTemplate Template:For.
- Glycine_encephalopathy wikiPageUsesTemplate Template:Infobox_Disease.
- Glycine_encephalopathy wikiPageUsesTemplate Template:Reflist.
- 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 hypernym Disorder.
- Glycine_encephalopathy type Disease.
- Glycine_encephalopathy type Defect.
- Glycine_encephalopathy type Disorder.
- Glycine_encephalopathy type Error.
- Glycine_encephalopathy type Pediatric.
- 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 wasDerivedFrom Glycine_encephalopathy?oldid=669409551.
- Glycine_encephalopathy depiction Glycin_-_Glycine.svg.
- Glycine_encephalopathy isPrimaryTopicOf Glycine_encephalopathy.