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| Term | immunodeficiency 116 | ID (Ontology) | DOID:0061082 (Human Disease) |
| Definition | A T cell deficiency that is characterized by the onset of recurrent upper and lower respiratory tract infections in infancy or early childhood and that has_material_basis_in homozygous mutation in the CD8-alpha gene on chromosome 2p12. | ||
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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___ primary immunodeficiency disease | |__T cell deficiency_____________| immunodeficiency 116 |
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| Is a |
autosomal recessive disease T cell deficiency |
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External Crossreferences & Linkouts
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| MIM:608957 | |||