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DO Term : X-linked lymphoproliferative syndrome 2 [DOID:0060706] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  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:
  • GARD:10916,
  • XIAP deficiency,
  • ICD10CM:D82.3,
  • 300635,
  • XLP2,
  • OMIM:300635
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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