Matches in DBpedia 2014 for { <http://dbpedia.org/resource/Pelger–Huet_anomaly> ?p ?o. }
Showing items 1 to 29 of
29
with 100 items per page.
- Pelger–Huet_anomaly abstract "Pelger–Huët anomaly (pronunciation: [pel′gər hyo̅o̅′ət]) is a blood laminopathy associated with the lamin B receptor.It is characterized by a white blood cell type known as a neutrophil whose nucleus is hyposegmented. It is a genetic disorder with an autosomal dominant inheritance pattern. Heterozygotes are clinically normal, although their neutrophils may be mistaken for immature cells which may cause mistreatment in a clinical setting. Homozygotes tend to have neutrophils with rounded nuclei that do have some functional problems.".
- Pelger–Huet_anomaly thumbnail Autosomal_dominant_-_en.svg?width=300.
- Pelger–Huet_anomaly wikiPageID "13494940".
- Pelger–Huet_anomaly wikiPageRevisionID "598668989".
- Pelger–Huet_anomaly diseasesdb "29515".
- Pelger–Huet_anomaly emedicinesubj "ped".
- Pelger–Huet_anomaly emedicinetopic "1753".
- Pelger–Huet_anomaly icd "288.2".
- Pelger–Huet_anomaly icd "D72.0".
- Pelger–Huet_anomaly meshid "D010381".
- Pelger–Huet_anomaly name "Pelger–Huët anomaly".
- Pelger–Huet_anomaly omim "169400".
- Pelger–Huet_anomaly subject Category:Autosomal_dominant_disorders.
- Pelger–Huet_anomaly subject Category:Cytoskeletal_defects.
- Pelger–Huet_anomaly type Disease.
- Pelger–Huet_anomaly type Situation.
- Pelger–Huet_anomaly comment "Pelger–Huët anomaly (pronunciation: [pel′gər hyo̅o̅′ət]) is a blood laminopathy associated with the lamin B receptor.It is characterized by a white blood cell type known as a neutrophil whose nucleus is hyposegmented. It is a genetic disorder with an autosomal dominant inheritance pattern. Heterozygotes are clinically normal, although their neutrophils may be mistaken for immature cells which may cause mistreatment in a clinical setting.".
- Pelger–Huet_anomaly label "Anomalia Pelgera-Hueta".
- Pelger–Huet_anomaly label "Anomalie de Pelger-Huet".
- Pelger–Huet_anomaly label "Pelger-Huët-Anomalie".
- Pelger–Huet_anomaly label "Pelger–Huet anomaly".
- Pelger–Huet_anomaly sameAs Pelger%E2%80%93Huet_anomaly.
- Pelger–Huet_anomaly sameAs Pelger-Huët-Anomalie.
- Pelger–Huet_anomaly sameAs Anomalie_de_Pelger-Huet.
- Pelger–Huet_anomaly sameAs Anomalia_Pelgera-Hueta.
- Pelger–Huet_anomaly sameAs Q975182.
- Pelger–Huet_anomaly sameAs Q975182.
- Pelger–Huet_anomaly wasDerivedFrom Pelger–Huet_anomaly?oldid=598668989.
- Pelger–Huet_anomaly depiction Autosomal_dominant_-_en.svg.