ZFIN Human Disease: lymphoproliferative syndrome 2

OBO ID: DOID:0060708

Term Name:	lymphoproliferative syndrome 2		Search Ontology:
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:	ICD10CM:D47.9 OMIM:615122
Ontology:	Human Disease ( DOID:0060708 )

Relationships

is a type of:	autosomal recessive disease lymphoproliferative syndrome autosomal recessive disease lymphoproliferative syndrome Show first 5 Terms

OTHER lymphoproliferative syndrome 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CD27	cd27	Lymphoproliferative syndrome 2	615122

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None