DISEASES

Disease-gene associations mined from literature

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