Search Ontology:
Human Disease
common variable immunodeficiency 7
- Term ID
- DOID:0081150
- Synonyms
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- Definition
- A common variable immunodeficiency that has_material_basis_in compound heterozygous mutation in the CD21 gene (CR2) on chromosome 1q32. https://pubmed.ncbi.nlm.nih.gov/22035880/
- References
- Ontology
- Human Disease ( DOID:0081150 )
- is a type of
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Genes Involved
Zebrafish Models