Search Ontology:
Human Disease

Pelger-Huet anomaly

Term ID
DOID:9631
Synonyms
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. https://www.ncbi.nlm.nih.gov/pubmed/12118250
References
Ontology
Human Disease   ( DOID:9631 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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