Term Name: lymphoproliferative syndrome 2
Synonyms: CD27 deficiency, LPFS2
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.
Ontology: Human Disease [DOID:0060708]   ( DOID:0060708 )

Relationships
is a type of: autosomal recessive disease lymphoproliferative syndrome