DISEASES

Disease-gene associations mined from literature

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 ...