About: nephrotic syndrome type 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 familial nephrotic syndrome nodeID://b50940840
label	nephrotic syndrome type 2
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0080379
database_cross_reference	OMIM:600995
has_exact_synonym	steroid-resistant autosomal recessive nephrotic syndrome (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A familial nephrotic syndrome characterized by steroid resistance and childhood onset of proteinuria, hypoalbuminemia, hyperlipidemia, and edema that has_material_basis_in homozygous or compound heterozygous mutation in the NPHS2 gene encoding podocin on chromosome 1q25-q31.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50940841

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