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Summary Literature (0)
MIM:209950 - IMMUNODEFICIENCY 27A; IMD27A

Xenbase Genes: il12b, stat1, ifngr2.1, ifngr2.2, ifngr1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008856 - immunodeficiency 27A
MONDO:0017901 - autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency
MONDO:0020530 - Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency

Disease Ontology (DO):
DOID:0111955 - immunodeficiency 27A