Search Ontology:
Human Disease
immunodeficiency 119
- Term ID
- DOID:0061085
- Synonyms
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- Definition
- A T cell, B cell, and NK cell deficiency that is characterized by the onset of recurrent upper and lower respiratory infections and warts in childhood and that has_material_basis_in homozygous mutation in the ICOSLG gene on chromosome 21q22. Affected individuals are susceptible to chronic DNA-based viral infections, including HPV and HSV. https://pubmed.ncbi.nlm.nih.gov/30498080/
- References
- Ontology
- Human Disease ( DOID:0061085 )
- is a type of
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Genes Involved
Zebrafish Models