Search Ontology:
Human Disease

immunodeficiency 15B

Term ID
DOID:0111959
Synonyms
  • 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. https://pubmed.ncbi.nlm.nih.gov/24369075/
References
Ontology
Human Disease   ( DOID:0111959 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models