immunodeficiency 73a with defective neutrophil chemotaxis and leukocytosis

Summary
Synonym
  • IMD73A
  • neutrophil immunodeficiency syndrome
Definition
A combined immunodeficiency characterized by onset of recurrent infections in early infancy, leukocytosis, neutrophilia, decreased TCR excision circles, decreased neutrophil chemotaxis, and T-cell abnormalities that has_material_basis_in heterozygous loss of function mutation in the RAC2 gene on chromosome 22q13.1.
Super Class
autosomal dominant disease combined immunodeficiency
Disease Ontology
DOID:0112064
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
5880 RAC2 Rac family small GTPase 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024