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Summary Literature (0)
MIM:616622 - IMMUNODEFICIENCY 42; IMD42

Xenbase Genes: rorc

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014710 - autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency

Disease Ontology (DO):
DOID:0111940 - immunodeficiency 42