Term Name:	immunodeficiency 32B
Synonyms:	autosomal recessive IRF8 deficiency, IMD32B, immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive
Definition:	A monocyte, dendritic cell, and NK cell deficiency characterized by defects in monocyte, dendritic cell, and natural killer (NK) cell development or function resulting recurrent infections particularly viral nfections that has_material_basis_in homozygous or compound heterozygous mutation in the IRF8 gene on chromosome 16q24.1.
Ontology:	Human Disease [DOID:0111985]   ( DOID:0111985 )