Search Ontology:
Human Disease

X-linked lymphoproliferative syndrome 2

Term ID
DOID:0060706
Synonyms
  • XIAP deficiency
  • XLP2
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. https://www.ncbi.nlm.nih.gov/pubmed/17080092
References
Ontology
Human Disease   ( DOID:0060706 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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