Search Ontology:
Human Disease
common variable immunodeficiency 14
- Term ID
- DOID:0081156
- Synonyms
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- Definition
- A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the IRF2BP2 gene on chromosome 1q42. https://pubmed.ncbi.nlm.nih.gov/27016798/
- References
- Ontology
- Human Disease ( DOID:0081156 )
- is a type of
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