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| Term | WHIM syndrome 2 | ID (Ontology) | DOID:0060973 (Human Disease) |
| Definition | An immunodeficiency disease that is characterized by chronic neutropenia and myelokathexis, which is impaired neutrophil mobilization from the bone marrow and that has_material_basis_in homozygous mutation in the CXCR2 gene on chromosome 2q35. | ||
| Also Known As | "WARTS, HYPOGAMMAGLOBULINEMIA, INFECTIONS, AND MYELOKATHEXIS SYNDROME 2" | ||
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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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autosomal genetic disease |__autosomal recessive disease_______ immune system disease | |__primary immunodeficiency disease__| WHIM syndrome 2 |
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autosomal recessive disease primary immunodeficiency disease |
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| MIM:619407 | |||