Search Ontology:
Human Disease

common variable immunodeficiency 10

Term ID
DOID:0081152
Synonyms
Definition
A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the NFKB2 gene on chromosome 10q24. https://pubmed.ncbi.nlm.nih.gov/24140114/
References
Ontology
Human Disease   ( DOID:0081152 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models