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Namespace Prefixes

Prefix	IRI
n7	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#
obo	http://www.geneontology.org/formats/oboInOwl#
n8	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_0050541

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_10595

rdfs:label

Charcot-Marie-Tooth disease type 4

rdfs:comment

Xref MGI. OMIM mapping confirmed by DO. [SN].

wdrs:describedby

n7:doid.owl

obo:id

DOID:0050541

obo:hasAlternativeId

DOID:0050582

obo:hasDbXref

GARD:12440 ORDO:64749

obo:hasExactSynonym

hereditary motor and sensory neuropathy

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_rare_slim

n2:IAO_0000115

A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.