Search Ontology:
Human Disease
common variable immunodeficiency 5
- Term ID
- DOID:0081148
- Synonyms
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- Definition
- A common variable immunodeficiency that has_material_basis_in homozygous mutation in the CD20 gene (MS4A1) on chromosome 11q13. https://pubmed.ncbi.nlm.nih.gov/20038800/
- References
- Ontology
- Human Disease ( DOID:0081148 )
- is a type of
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