| Metadata | |
|---|---|
| ID | DOID:0060973 |
| Name | WHIM syndrome 2 |
| 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. https://pubmed.ncbi.nlm.nih.gov/24777453/ |
| Xrefs | |
| Synonyms |
WARTS, HYPOGAMMAGLOBULINEMIA, INFECTIONS, AND MYELOKATHEXIS SYNDROME 2 [EXACT] |
| Parent Relationships |