Search Ontology:
Human Disease

common variable immunodeficiency 13

Term ID
DOID:0081155
Synonyms
Definition
A common variable immunodeficiency that is characterized by recurrent bacterial infections, mainly affecting the respiratory tract, and associated with hypogammaglobulinemia and decreased numbers of B cells and that has_material_basis_in heterozygous mutation in the IKZF1 gene on chromosome 7p12. https://pubmed.ncbi.nlm.nih.gov/26981933/
References
Ontology
Human Disease   ( DOID:0081155 )
Relationships
is a type of
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Genes Involved
Zebrafish Models