OBO ID: DOID:9631
Term Name: Pelger-Huet anomaly Search Ontology:
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 Pelger-Huet anomaly PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LBR Pelger-Huet anomaly 169400
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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