This HTML5 document contains 19 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n8	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2	http://purl.obolibrary.org/obo/
wdrs	http://www.w3.org/2007/05/powder-s#
rdfs	http://www.w3.org/2000/01/rdf-schema#
skos	http://www.w3.org/2004/02/skos/core#
obo	http://www.geneontology.org/formats/oboInOwl#
n4	http://purl.obolibrary.org/obo/doid#
rdf	http://www.w3.org/1999/02/22-rdf-syntax-ns#
owl	http://www.w3.org/2002/07/owl#
xsdh	http://www.w3.org/2001/XMLSchema#

Statements

Subject Item

n2:DOID_9120

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0014667

rdfs:label

amyloidosis

rdfs:comment

amyloidosis has both inherited and aquired subtypes [LS].

skos:exactMatch

MESH:D000686

wdrs:describedby

n8:doid.owl

obo:id

DOID:9120

obo:hasDbXref

ICD9CM:277.3 SNOMEDCT_US_2021_09_01:154769007 ICD10CM:E85 MESH:D000686 NCI:C2868 UMLS_CUI:C0002726

obo:hasExactSynonym

amyloid disease

obo:hasOBONamespace

disease_ontology

obo:inSubset

n4:NCIthesaurus n4:DO_MGI_slim n4:DO_FlyBase_slim

n2:IAO_0000115

A disease of metabolsism that is characterized by extracellular tissue deposition of mis-folded amyloid fibrils built up by twisted protofilaments, deposited in the spaces between the cells of vital organs, causing disruption of organ tissue structure and function. These deposits may result in a wide range of clinical manifestations depending upon their type, location, and the amount of deposition.