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| Term | immunodeficiency 65 | ID (Ontology) | DOID:0111978 (Human Disease) |
| 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. | ||
| Also Known As | "IMD65" ; "immunodeficiency 65, susceptibility to viral infections" | ||
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| DO.org | |||
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autosomal genetic disease |__autosomal recessive disease_______ immune system disease | |__primary immunodeficiency disease__| immunodeficiency 65 |
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| Is a |
autosomal recessive disease primary immunodeficiency disease |
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| MIM:618648 | |||