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Summary Literature (0)
DOID:0060706 - X-linked lymphoproliferative syndrome 2


Disease Ontology Definition:A lymphoproliferative syndrome characterized by X-linked inheritance, immune dysregulation after viral infect that may include lymphohystiocytosis, hypogammaglobulinemia and/or splenomegaly and that has_material_basis_in mutation in the XIAP gene on chromosome Xq25.

Synonyms: XIAP deficiency, XLP2

Xenbase Genes : xiap

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010385 - X-linked lymphoproliferative disease due to XIAP deficiency

OMIM:
OMIM:300635 - LYMPHOPROLIFERATIVE SYNDROME, X-LINKED, 2; XLP2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): lymphoproliferative syndrome (is_a)