Term Name:	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
Synonyms:	IMD73C
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.
Ontology:	Human Disease [DOID:0112062]   ( DOID:0112062 )