Search Ontology:
Human Disease

immunodeficiency 33

Term ID
DOID:0112003
Synonyms
  • IMD33
  • X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
  • X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency
  • X-linked MSMD due to IKBKG deficiency
  • X-linked MSMD due to NEMO deficiency
Definition
A combined immunodeficiency characterized by early-onset severe infection and variable immunological abnormalities that has_material_basis_in hemizygous mutation in the IKBKG gene on chromosome Xq28. (2)
References
Ontology
Human Disease   ( DOID:0112003 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models