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Concept information

disease > genetic disease > hereditary disease > Pelger-Huet anomaly
disease > immunopathology > leukocyte disease > Pelger-Huet anomaly
disease > hemopathy > leukocyte disease > Pelger-Huet anomaly

Preferred term

Pelger-Huet anomaly  

Definition

  • Pelger–Huët anomaly 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. (Wikipedia)

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URI

http://data.loterre.fr/ark:/67375/VH8-X9VP93T2-D

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