OBO ID: DOID:0111978 |
Term Name: | immunodeficiency 65 | Search Ontology: | |
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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 the IRF9 gene on chromosome 14q12. (2) | ||
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Ontology: | Human Disease ( DOID:0111978 ) |
OTHER immunodeficiency 65 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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