Term Name:	immunodeficiency 32A
Synonyms:	IMD32A, immunodeficiency 32A, mycobacteriosis, autosomal dominant, Mendelian susceptibility to mycobacterial diseases due to partial interferon regulatory factor 8 deficiency, Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency, MSMD due to partial interferon regulatory factor 8 deficiency, MSMD due to partial IRF8 deficiency
Definition:	A dendritic cell deficiency characterized by marked loss of CD11C-positive/CD1C dendritic cells and increased susceptibility to mycobacterial infections that has_material_basis_in heterozygous mutation in the IRF8 gene on chromosome 16q24.1.
Ontology:	Human Disease [DOID:0111986]   ( DOID:0111986 )