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Namespace Prefixes

PrefixIRI
n7https://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#
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_0112107
rdf:type
owl:Class
rdfs:subClassOf
n2:DOID_0050765 n2:DOID_0050735 _:vb50946094
rdfs:label
McLeod syndrome
wdrs:describedby
n7:doid.owl
obo:id
DOID:0112107
obo:hasDbXref
ORDO:59306 OMIM:300842 MESH:C564038 SNOMEDCT_US_2021_09_01:234411007 GARD:10731 UMLS_CUI:C0398568
obo:hasExactSynonym
X-linked McLeod syndrome McLeod neuroacanthocytosis syndrome McLeod syndrome with or without chronic granulomatous disease McLeod type neuroacanthocytosis MLS
obo:hasOBONamespace
disease_ontology
n2:IAO_0000115
A neuroacanthocytosis characterized by absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, compensated hemolysis, and involuntary movements that has_material_basis_in mutation in XK on chromosome Xp21.1.
Subject Item
_:vb50946094
rdf:type
owl:Restriction
owl:onProperty
n2:IDO_0000664
owl:someValuesFrom
n2:GENO_0000936
wdrs:describedby
n7:doid.owl