About: nephrotic syndrome type 7

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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 familial nephrotic syndrome nodeID://b50940858
label	nephrotic syndrome type 7
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080388
database_cross_reference	OMIM:615008 ORDO:329903
has_exact_synonym	Ig-mediated MPGN (en) Immunoglobulin-mediated MPGN (en) nephrotic syndrome type 7 with membranoptoliferative glomerulonephritis (en) immunoglobulin-mediated membranoproliferative glomerulonephritis (en) Ig-mediated membranoproliferative glomerulonephritis (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A familial nephrotic syndrome characterized by onset in the first decade of life of progressive renal disease with proteinuria and membranoproliferative glomerulonephritis that has_material_basis_in homozygous or compound heterozygous mutation in the DGKE gene on chromosome 17q22.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50940859

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