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- Q975182 subject Q6853345.
- Q975182 subject Q7216519.
- Q975182 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.".
- Q975182 icd10 "D72.0".
- Q975182 icd9 "288.2".
- Q975182 meshId "D010381".
- Q975182 omim "169400".
- Q975182 thumbnail Autosomal_dominant_-_en.svg?width=300.
- Q975182 wikiPageWikiLink Q1137767.
- Q975182 wikiPageWikiLink Q12156.
- Q975182 wikiPageWikiLink Q14911836.
- Q975182 wikiPageWikiLink Q186380.
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- Q975182 wikiPageWikiLink Q244570.
- Q975182 wikiPageWikiLink Q264118.
- Q975182 wikiPageWikiLink Q2915477.
- Q975182 wikiPageWikiLink Q3216770.
- Q975182 wikiPageWikiLink Q3234995.
- Q975182 wikiPageWikiLink Q371520.
- Q975182 wikiPageWikiLink Q40260.
- Q975182 wikiPageWikiLink Q42395.
- Q975182 wikiPageWikiLink Q467635.
- Q975182 wikiPageWikiLink Q478389.
- Q975182 wikiPageWikiLink Q4854514.
- Q975182 wikiPageWikiLink Q6531938.
- Q975182 wikiPageWikiLink Q6534506.
- Q975182 wikiPageWikiLink Q6853345.
- Q975182 wikiPageWikiLink Q7216519.
- Q975182 wikiPageWikiLink Q729735.
- Q975182 wikiPageWikiLink Q922411.
- Q975182 wikiPageWikiLink Q954625.
- Q975182 wikiPageWikiLink Q966229.
- Q975182 icd "288.2".
- Q975182 icd "D72.0".
- Q975182 meshid "D010381".
- Q975182 name "Pelger–Huët anomaly".
- Q975182 omim "169400".
- Q975182 type Disease.
- Q975182 type Thing.
- Q975182 type Q12136.
- Q975182 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.".
- Q975182 label "Pelger–Huet anomaly".
- Q975182 depiction Autosomal_dominant_-_en.svg.
- Q975182 name "Pelger–Huët anomaly".