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Namespace Prefixes

PrefixIRI
n8https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/
n2http://purl.obolibrary.org/obo/
wdrshttp://www.w3.org/2007/05/powder-s#
rdfshttp://www.w3.org/2000/01/rdf-schema#
obohttp://www.geneontology.org/formats/oboInOwl#
n4http://purl.obolibrary.org/obo/doid#
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
owlhttp://www.w3.org/2002/07/owl#
xsdhhttp://www.w3.org/2001/XMLSchema#

Statements

Subject Item
n2:DOID_10595
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_440
rdfs:label
Charcot-Marie-Tooth disease
wdrs:describedby
n8:doid.owl
obo:id
DOID:10595
obo:hasDbXref
ICD10CM:G60.0 SNOMEDCT_US_2021_09_01:193158000 NCI:C75467 OMIM:PS118220 GARD:6034 UMLS_CUI:C0007959 MESH:D002607 ICD9CM:356.1
obo:hasExactSynonym
CMT - Charcot-Marie-Tooth disease
obo:hasOBONamespace
disease_ontology
obo:inSubset
n4:NCIthesaurus n4:DO_FlyBase_slim
n2:IAO_0000115
A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm.