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common variable immunodeficiency 4
Summary
- Definition
- A common variable immunodeficiency that has_material_basis_in homozygous mutation in the BAFFR gene (TNFRSF13C), which encodes the B-cell activating factor receptor, on chromosome 22q13.
- Super Class
- common variable immunodeficiency
External Links
- Disease Ontology
- DOID:0081147
- Mondo Disease Ontology
- OMIM
