Categories: Haematopoietic system phene

Possible human homologue (MIM number): 610007 (gene)

Links to MONDO diseases: No links.

Cross-species summary: This phenotype is characterized by hyposegmented nuclei of granulocytes. The phenotype resembles Pelger-Huët anomaly, but is caused by variants in the LMBR1L gene.

Species in which this phene is found:
dog (Canis lupus familiaris)