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 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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