Search Ontology:
Human Disease
common variable immunodeficiency 10
- Term ID
- DOID:0081152
- Synonyms
-
- Definition
- A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24. https://pubmed.ncbi.nlm.nih.gov/24140114/
- References
- Ontology
- Human Disease ( DOID:0081152 )
- is a type of
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