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| Term | immunodeficiency 69 | ID (Ontology) | DOID:0112006 (Human Disease) |
| Definition | A T cell and NK cell immunodeficiency characterized by increased susceptibility to disseminated mycobacterial infection and failure of T and NK cells to produce gamma-interferon when stimulated in vitro that has_material_basis_in homozygous or compound heterozygous mutation in the IFNG gene on chromosome 12q15. | ||
| Also Known As | "IMD69" | ||
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| DO.org | |||
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autosomal genetic disease |__autosomal recessive disease__________ primary immunodeficiency disease | |__T cell and NK cell immunodeficiency__| immunodeficiency 69 |
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| Is a |
autosomal recessive disease T cell and NK cell immunodeficiency |
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| MIM:618963 | |||