OBO ID: DOID:0081145
Term Name: common variable immunodeficiency 2 Search Ontology:
Synonyms:
Definition: A common variable immunodeficiency that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the TNFRSF13B gene, which encodes the transmembrane activator and CAML interactor (TACI), on chromosome 17p11.2. https://pubmed.ncbi.nlm.nih.gov/16007087/
References:
Ontology: Human Disease   ( DOID:0081145 )
Relationships
is a type of:
OTHER common variable immunodeficiency 2 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TNFRSF13B Immunodeficiency, common variable, 2
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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