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Summary Literature (0)
MIM:615978 - IMMUNODEFICIENCY 27B; IMD27B

Xenbase Genes: ifngr1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014429 - autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency

Disease Ontology (DO):
DOID:0111956 - immunodeficiency 27B