Search Ontology:
Human Disease
immunodeficiency 15B
- Term ID
- DOID:0111959
- Synonyms
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- 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
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- MIM:615592
- UMLS_CUI:C4747743
- Ontology
- Human Disease ( DOID:0111959 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models