Pelger-Huet Anomaly, also known as pelger-huët anomaly, is related to osteochondrodysplasia and muscular dystrophy. An important gene associated with Pelger-Huet Anomaly is LBR (Lamin B Receptor), and among its related pathways/superpathways are Cell Cycle, Mitotic and Golgi-to-ER retrograde transport. Affiliated tissues include neutrophil and bone marrow, and related phenotypes are abnormality of neutrophils and abnormality of chromosome segregation