|OBO ID: DOID:0111978|
|Term Name:||immunodeficiency 65||Search Ontology:|
|Definition:||A primary immunodeficiency disease characterized by onset in early infancy of recurrent and severe viral infections, impaired cellular type I interferon response, and poor outcomes after vaccination with live attenuated vaccines that has_material_basis_in homozygous or compound heterozygous mutation in IRF9 on chromosome 14q12. (2)|
|Ontology:||Human Disease (DOID:0111978)|
|is a type of:||
OTHER immunodeficiency 65 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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