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| Term | hereditary neutrophilia | ID (Ontology) | DOID:0090120 (Human Disease) |
| Definition | A leukocyte disease characterized by autosomal dominant inheritance of lifelong, persistent elevated neutrophil counts primarily consisting of segmented neutrophils that has_material_basis_in heterozygous mutation in the colony stimulating factor 3 receptor (CSF3R) gene on chromosome 1p34. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ hematopoietic system disease | |__leukocyte disease___________| hereditary neutrophilia |
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Relationships
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| Is a |
autosomal dominant disease leukocyte disease |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:C563010 MIM:162830 ORDO:279943 SNOMEDCT_US_2023_03_01:129639005 UMLS_CUI:C0543669 |
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