Search Ontology:
Human Disease

common variable immunodeficiency 11

Term ID
DOID:0081153
Synonyms
Definition
A common variable immunodeficiency that has_material_basis_in homozygous mutation in the IL21 gene on chromosome 4q27. https://pubmed.ncbi.nlm.nih.gov/24746753/
References
Ontology
Human Disease   ( DOID:0081153 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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