Search Ontology:
Human Disease

common variable immunodeficiency 3

Term ID
DOID:0081146
Synonyms
Definition
A common variable immunodeficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CD19 gene on chromosome 16p11.2. https://pubmed.ncbi.nlm.nih.gov/16672701/
References
Ontology
Human Disease   ( DOID:0081146 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models