Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Enolase_deficiency> ?p ?o }
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- Enolase_deficiency abstract "Enolase Deficiency is a rare genetic disorder of glucose metabolism. Partial deficiencies have been observed in several caucasian families. The deficiency is transmitted through an autosomal dominant inheritance pattern. The gene for Enolase 1 has been localized to Chromosome 1 in humans. Enolase deficiency, like other glycolytic enzyme deficiences, usually manifests in red blood cells as they rely entirely on anaerobic glycolysis. Enolase deficiency is associated with a spherocytic phenotype and can result in hemolytic anemia, which is responsible for the clinical signs of Enolase deficiency.".
- Enolase_deficiency icd10 "E74.0".
- Enolase_deficiency omim "172430".
- Enolase_deficiency wikiPageID "20685304".
- Enolase_deficiency wikiPageLength "5523".
- Enolase_deficiency wikiPageOutDegree "18".
- Enolase_deficiency wikiPageRevisionID "671033944".
- Enolase_deficiency wikiPageWikiLink Alpha-enolase.
- Enolase_deficiency wikiPageWikiLink Amino_acid.
- Enolase_deficiency wikiPageWikiLink Anaerobic_glycolysis.
- Enolase_deficiency wikiPageWikiLink Carbohydrate_metabolism.
- Enolase_deficiency wikiPageWikiLink Category:Inborn_errors_of_carbohydrate_metabolism.
- Enolase_deficiency wikiPageWikiLink Caucasian_race.
- Enolase_deficiency wikiPageWikiLink Chromosome_1_(human).
- Enolase_deficiency wikiPageWikiLink Dissociation_(chemistry).
- Enolase_deficiency wikiPageWikiLink Dominance_(genetics).
- Enolase_deficiency wikiPageWikiLink Embryo.
- Enolase_deficiency wikiPageWikiLink Genetic_disorder.
- Enolase_deficiency wikiPageWikiLink Glycolysis.
- Enolase_deficiency wikiPageWikiLink Hemolytic_anemia.
- Enolase_deficiency wikiPageWikiLink Human.
- Enolase_deficiency wikiPageWikiLink Mutation.
- Enolase_deficiency wikiPageWikiLink Myalgia.
- Enolase_deficiency wikiPageWikiLink Phenotype.
- Enolase_deficiency wikiPageWikiLink Red_blood_cell.
- Enolase_deficiency wikiPageWikiLinkText "Enolase deficiency".
- Enolase_deficiency icd "E74.0".
- Enolase_deficiency name "Enolase deficiency".
- Enolase_deficiency omim "172430".
- Enolase_deficiency wikiPageUsesTemplate Template:Carbohydrate_metabolic_pathology.
- Enolase_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- Enolase_deficiency wikiPageUsesTemplate Template:Reflist.
- Enolase_deficiency subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Enolase_deficiency hypernym Disorder.
- Enolase_deficiency type Disease.
- Enolase_deficiency type Error.
- Enolase_deficiency type Thing.
- Enolase_deficiency type Q12136.
- Enolase_deficiency comment "Enolase Deficiency is a rare genetic disorder of glucose metabolism. Partial deficiencies have been observed in several caucasian families. The deficiency is transmitted through an autosomal dominant inheritance pattern. The gene for Enolase 1 has been localized to Chromosome 1 in humans. Enolase deficiency, like other glycolytic enzyme deficiences, usually manifests in red blood cells as they rely entirely on anaerobic glycolysis.".
- Enolase_deficiency label "Enolase deficiency".
- Enolase_deficiency sameAs Q5379381.
- Enolase_deficiency sameAs m.0520rty.
- Enolase_deficiency sameAs Q5379381.
- Enolase_deficiency wasDerivedFrom Enolase_deficiency?oldid=671033944.
- Enolase_deficiency isPrimaryTopicOf Enolase_deficiency.
- Enolase_deficiency name "Enolase deficiency".