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| Term | immunodeficiency 127 | ID (Ontology) | DOID:0061092 (Human Disease) |
| Definition | A primary immunodeficiency disease that is characterized by increased susceptibility to recurrent pulmonary infection with Mycobacterium tuberculosis and that has_material_basis_in homozygous mutation in the TNF gene on chromosome 6p21. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease_______ immune system disease | |__primary immunodeficiency disease__| immunodeficiency 127 |
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| Is a |
autosomal recessive disease primary immunodeficiency disease |
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External Crossreferences & Linkouts
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| MIM:620977 | |||