immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia (DOID:0112062)
Alliance: disease page
Synonyms: IMD73C
Alt IDs: OMIM:618987
Definition: A combined immunodeficiency characterized by onset of recurrent infection in early childhood, impaired neutrophil chemotaxis, decreased B cells, hypogammaglobulinemia, and other variable features that has_material_basis_in homozygous or compound heterozygous mutation in the RAC2 gene on chromosome 22q12.