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Metadata
ID	DOID:0112062
Name	immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia
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. https://pubmed.ncbi.nlm.nih.gov/25512081/
Xrefs	MIM:618987
Synonyms	IMD73C [EXACT]
Parent Relationships	is_a combined immunodeficiency is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance