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| Term | immunodeficiency 79 | ID (Ontology) | DOID:0112277 (Human Disease) |
| Definition | A T cell deficiency characterized by childhood onset of recurrent and recalcitrant skin warts due to uncontrolled viral infection with human papillomavirus and absence of the CD4 antigen on T cells, monocytes, and dendritic cells that has_material_basis_in homozygous or compound heterozygous mutation in CD4 on chromosome 12p13. | ||
| Also Known As | "IMD79" | ||
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| DO.org | |||
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autosomal genetic disease |__autosomal recessive disease___ primary immunodeficiency disease | |__T cell deficiency_____________| immunodeficiency 79 |
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| Is a |
autosomal recessive disease T cell deficiency |
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| MIM:619238 | |||