Human genes for lymphoproliferative syndrome 2
Lymphoproliferative syndrome 2 [DOID:0060708]
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.
Synonyms: lymphoproliferative syndrome 2, DOID:0060708, CD27 deficiency, LPFS2