Search Ontology:
Human Disease
common variable immunodeficiency 11
- Term ID
- DOID:0081153
- Synonyms
-
- Definition
- A common variable immunodeficiency that has_material_basis_in homozygous mutation in the IL21 gene on chromosome 4q27. https://pubmed.ncbi.nlm.nih.gov/24746753/
- References
- Ontology
- Human Disease ( DOID:0081153 )
- is a type of
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