OBO ID: DOID:0081156
Term Name: common variable immunodeficiency 14 Search Ontology:
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 common variable immunodeficiency 14 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
IRF2BP2 ?Immunodeficiency, common variable, 14 617765
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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