Human genes for Pelger-Huet anomaly
Pelger-Huet anomaly [DOID:9631]
A hematopoietic system disease characterized by white blood cells with unusually shaped nuclei that has_material_basis_in heterozygous mutation in LBR on chromosome 1q42.12.
Synonyms: Pelger-Huet anomaly, DOID:9631, PelgerHuet anomaly, Pelger-Huet anomalies
Linkouts: OMIM