About: immunodeficiency 19

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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 severe combined immunodeficiency nodeID://b50945838
label	immunodeficiency 19
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111972
database_cross_reference	OMIM:615617 UMLS_CUI:C3810147
has_exact_synonym	SCID T cell-negative, B cell-positive, NK cell-positive CD3-delta deficiency IMD19 severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A severe combined immunodeficiency characterized by onset in early infancy of recurrent bacterial, viral, and fungal infections with a T cell-negative, B cell-positive, natural killer cell-positive immune cell phenotype that has_material_basis_in homozygous or compound heterozygous mutation in CD3D on chromosome 11q23.3.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50945839

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