immunodeficiency 15B

Summary
Synonym
  • IMD15B
Definition
A severe combined immunodeficiency characterized by onset in infancy of life-threatening bacterial, fungal, and viral infections, failure to thrive, impaired differentiation and activation of immune cells, and hypo- or agammaglobulinemia but relatively normal B and T cell numbers that has_material_basis_in homozygous or compound heterozygous mutation in the IKBKB gene on chromosome 8p11.21.
Super Class
autosomal recessive disease severe combined immunodeficiency
External Links
Disease Ontology
DOID:0111959
Mondo Disease Ontology
UMLS
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3551 IKBKB inhibitor of nuclear factor kappa B kinase subunit beta
Displaying 1 entry
Gene ID Gene Symbol Description Source
16150 Ikbkb inhibitor of kappaB kinase beta

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024