Search Ontology:
Human Disease
common variable immunodeficiency 6
- Term ID
- DOID:0081149
- Synonyms
-
- Definition
- A common variable immunodeficiency that has_material_basis_in homozygous mutation in the CD81 gene on chromosome 11p. https://pubmed.ncbi.nlm.nih.gov/20237408/
- References
- Ontology
- Human Disease ( DOID:0081149 )
- is a type of
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