Search Ontology:
Human Disease

lymphoproliferative syndrome 2

Term ID
DOID:0060708
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. (2)
References
Ontology
Human Disease   ( DOID:0060708 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models