Human genes for WHIM syndrome
WHIM syndrome [DOID:0060591]
An immunodeficiency disease that is characterized by neutropenia, hypogammaglobulinemia, and extensive human papillomavirus infection and that has_material_basis_in heterozygous mutation in the CXCR4 gene on chromosome 2q22.
Synonyms: WHIM syndrome, DOID:0060591, WHIM disease, WHIM disorder, WHIM syndromes ...