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Summary Literature (1)
DOID:9631 - Pelger-Huet anomaly

Disease Ontology Definition: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:

Xenbase Genes : lbr

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008214 - Pelger-Huet anomaly


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), hematopoietic system disease (is_a)