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Summary Literature (0)
MIM:613500 - AGAMMAGLOBULINEMIA 2, AUTOSOMAL RECESSIVE; AGM2

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011096 - lacrimal nerve
MONDO:0013287 - agammaglobulinemia 2, autosomal recessive
MONDO:0016462 - periorbital skin

Disease Ontology (DO):
DOID:0081135 - agammaglobulinemia 2
DOID:2583 - agammaglobulinemia