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Summary Literature (0)
MIM:618131 - IMMUNODEFICIENCY 58; IMD58

Xenbase Genes: carmil2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0029134 - severe combined immunodeficiency due to CARMIL2 deficiency

Disease Ontology (DO):
DOID:0111984 - immunodeficiency 58