Search Ontology:
Human Disease
common variable immunodeficiency 3
- Term ID
- DOID:0081146
- Synonyms
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- Definition
- A common variable immunodeficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CD19 gene on chromosome 16p11.2. https://pubmed.ncbi.nlm.nih.gov/16672701/
- References
- Ontology
- Human Disease ( DOID:0081146 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models