Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Enolase_deficiency> ?p ?o. }
Showing items 1 to 39 of
39
with 100 items per page.
- 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 wikiPageRevisionID "603013617".
- Enolase_deficiency hasPhotoCollection Enolase_deficiency.
- Enolase_deficiency icd "E74.0".
- Enolase_deficiency name "Enolase deficiency".
- Enolase_deficiency omim "172430".
- Enolase_deficiency subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Enolase_deficiency type Abstraction100002137.
- Enolase_deficiency type Act100030358.
- Enolase_deficiency type Attribute100024264.
- Enolase_deficiency type Condition113920835.
- Enolase_deficiency type Disease114070360.
- Enolase_deficiency type Event100029378.
- Enolase_deficiency type IllHealth114052046.
- Enolase_deficiency type Illness114061805.
- Enolase_deficiency type InbornErrorsOfCarbohydrateMetabolism.
- Enolase_deficiency type Mistake100070965.
- Enolase_deficiency type Nonaccomplishment100066216.
- Enolase_deficiency type PathologicalState114051917.
- Enolase_deficiency type PhysicalCondition114034177.
- Enolase_deficiency type PsychologicalFeature100023100.
- Enolase_deficiency type State100024720.
- Enolase_deficiency type YagoPermanentlyLocatedEntity.
- Enolase_deficiency type Disease.
- Enolase_deficiency type AilmentCondition.
- Enolase_deficiency type Situation.
- 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 m.0520rty.
- Enolase_deficiency sameAs Q5379381.
- Enolase_deficiency sameAs Q5379381.
- Enolase_deficiency sameAs 366.
- Enolase_deficiency sameAs Enolase_deficiency.
- Enolase_deficiency wasDerivedFrom Enolase_deficiency?oldid=603013617.
- Enolase_deficiency isPrimaryTopicOf Enolase_deficiency.
- Enolase_deficiency name "Enolase deficiency".