Search Ontology:
Human Disease
immunodeficiency 116
- Term ID
- DOID:0061082
- Synonyms
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- Definition
- A T cell deficiency that is characterized by the onset of recurrent upper and lower respiratory tract infections in infancy or early childhood and that has_material_basis_in homozygous mutation in the CD8-alpha gene on chromosome 2p12. https://pubmed.ncbi.nlm.nih.gov/26563160/
- References
- Ontology
- Human Disease ( DOID:0061082 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models