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Summary Literature (0)
MIM:603554 - OMENN SYNDROME

Xenbase Genes: rag2, dclre1c, rag1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011225 - severe combined immunodeficiency due to DCLRE1C deficiency
MONDO:0011338 - Omenn syndrome

Disease Ontology (DO):
DOID:0060010 - Omenn syndrome