OBO ID: DOID:9631 |
Term Name: | Pelger-Huet anomaly | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:9631 ) |
OTHER Pelger-Huet anomaly PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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