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Metadata
ID	DOID:0112061
Name	immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia
Definition	A combined immunodeficiency characterized by onset of recurrent infections in infancy or early childhood and variable immune system abnormalities including B- and T-cell lymphopenia, decreased immunoglobulin subsets, decreased TCR excision circles and dysfunctional T cells, decreased NK cells, neutropenia, and impaired neutrophil chemotaxis that has_material_basis_in heterozygous gain-of-function mutation in the RAC2 gene on chromosome 22q13.1. https://pubmed.ncbi.nlm.nih.gov/32542921/, https://pubmed.ncbi.nlm.nih.gov/30723080/
Xrefs	MIM:618986
Synonyms	IMD73B [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a combined immunodeficiency
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance