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- 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 icd10 "D72.0".
- Pelger–Huet_anomaly icd9 "288.2".
- Pelger–Huet_anomaly meshId "D010381".
- Pelger–Huet_anomaly omim "169400".
- Pelger–Huet_anomaly thumbnail Autosomal_dominant_-_en.svg?width=300.
- Pelger–Huet_anomaly wikiPageID "13494940".
- Pelger–Huet_anomaly wikiPageLength "6800".
- Pelger–Huet_anomaly wikiPageOutDegree "32".
- Pelger–Huet_anomaly wikiPageRevisionID "695910283".
- Pelger–Huet_anomaly wikiPageWikiLink Acute_myeloid_leukemia.
- Pelger–Huet_anomaly wikiPageWikiLink Autosome.
- Pelger–Huet_anomaly wikiPageWikiLink Bandemia.
- Pelger–Huet_anomaly wikiPageWikiLink Category:Autosomal_dominant_disorders.
- Pelger–Huet_anomaly wikiPageWikiLink Category:Cytoskeletal_defects.
- Pelger–Huet_anomaly wikiPageWikiLink Cell_nucleus.
- Pelger–Huet_anomaly wikiPageWikiLink Chronic_myelogenous_leukemia.
- Pelger–Huet_anomaly wikiPageWikiLink Dominance_(genetics).
- Pelger–Huet_anomaly wikiPageWikiLink Folate_deficiency.
- Pelger–Huet_anomaly wikiPageWikiLink Genetic_disorder.
- Pelger–Huet_anomaly wikiPageWikiLink Hypopituitarism.
- Pelger–Huet_anomaly wikiPageWikiLink Kyphosis.
- Pelger–Huet_anomaly wikiPageWikiLink Lamin_B_receptor.
- Pelger–Huet_anomaly wikiPageWikiLink Laminopathy.
- Pelger–Huet_anomaly wikiPageWikiLink Leukemoid_reaction.
- Pelger–Huet_anomaly wikiPageWikiLink Malaria.
- Pelger–Huet_anomaly wikiPageWikiLink Metacarpal_bones.
- Pelger–Huet_anomaly wikiPageWikiLink Multiple_myeloma.
- Pelger–Huet_anomaly wikiPageWikiLink Muscular_dystrophy.
- Pelger–Huet_anomaly wikiPageWikiLink Myelodysplastic_syndrome.
- Pelger–Huet_anomaly wikiPageWikiLink Myxedema.
- Pelger–Huet_anomaly wikiPageWikiLink Neutrophil_granulocyte.
- Pelger–Huet_anomaly wikiPageWikiLink Pince-nez.
- Pelger–Huet_anomaly wikiPageWikiLink Polydactyly.
- Pelger–Huet_anomaly wikiPageWikiLink Valproate.
- Pelger–Huet_anomaly wikiPageWikiLink Vitamin_B12_deficiency.
- Pelger–Huet_anomaly wikiPageWikiLink White_blood_cell.
- Pelger–Huet_anomaly wikiPageWikiLink File:Autosomal_dominant_-_en.svg.
- Pelger–Huet_anomaly wikiPageWikiLinkText "Pelger–Huet anomaly".
- 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 wikiPageUsesTemplate Template:Cytoskeletal_defects.
- Pelger–Huet_anomaly wikiPageUsesTemplate Template:Fact.
- Pelger–Huet_anomaly wikiPageUsesTemplate Template:Hematology.
- Pelger–Huet_anomaly wikiPageUsesTemplate Template:Infobox_disease.
- Pelger–Huet_anomaly wikiPageUsesTemplate Template:Reflist.
- Pelger–Huet_anomaly subject Category:Autosomal_dominant_disorders.
- Pelger–Huet_anomaly subject Category:Cytoskeletal_defects.
- Pelger–Huet_anomaly hypernym Laminopathy.
- Pelger–Huet_anomaly type Disease.
- Pelger–Huet_anomaly type Defect.
- Pelger–Huet_anomaly type Disorder.
- Pelger–Huet_anomaly type Redirect.
- Pelger–Huet_anomaly type Thing.
- Pelger–Huet_anomaly type Q12136.
- 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 "Pelger–Huet anomaly".
- Pelger–Huet_anomaly sameAs Q975182.
- 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 m.03m3wmm.
- Pelger–Huet_anomaly sameAs Q975182.
- Pelger–Huet_anomaly wasDerivedFrom Pelger–Huet_anomaly?oldid=695910283.
- Pelger–Huet_anomaly depiction Autosomal_dominant_-_en.svg.
- Pelger–Huet_anomaly isPrimaryTopicOf Pelger–Huet_anomaly.
- Pelger–Huet_anomaly name "Pelger–Huët anomaly".