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Summary Literature (0)
MIM:614889 - IMMUNODEFICIENCY 28; IMD28

Xenbase Genes: ifngr2.1, ifngr2.2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013953 - immunodeficiency 28
MONDO:0017900 - autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency
MONDO:0017902 - autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency

Disease Ontology (DO):
DOID:0111995 - immunodeficiency 28