About: lymphoproliferative syndrome 2

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal recessive disease lymphoproliferative syndrome nodeID://b50939242
label	lymphoproliferative syndrome 2
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060708
database_cross_reference	ICD10CM:D47.9 OMIM:615122
has_exact_synonym	CD27 deficiency (en) LPFS2 (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	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.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939243

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