Search Ontology:
Human Disease

common variable immunodeficiency 14

Term ID
DOID:0081156
Synonyms
Definition
A common variable immunodeficiency that has_material_basis_in heterozygous mutation in the IRF2BP2 gene on chromosome 1q42. https://pubmed.ncbi.nlm.nih.gov/27016798/
References
Ontology
Human Disease   ( DOID:0081156 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models