|OBO ID: DOID:0060708|
|Term Name:||lymphoproliferative syndrome 2||Search Ontology:|
|Definition:||A lymphoproliferative syndrome characterized by autosomal recessive inheritance, persistent symptomatic Epstein-Barr virus-associated viremia, hypogammaglobulinemia, and impairment in specific antibody function and that has_material_basis_in homozygous mutation in the CD27 gene on chromosome 12p13. (2)|
|Ontology:||Human Disease (DOID:0060708)|
|is a type of:||
OTHER lymphoproliferative syndrome 2 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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