This HTML5 document contains 28 embedded RDF statements represented using HTML+Microdata notation.

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Namespace Prefixes

Prefix	IRI
n5	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_14711

rdf:type

owl:Class

rdfs:subClassOf

_:vb50949725 n2:DOID_0080012 n2:DOID_225

rdfs:label

FG syndrome

rdfs:comment

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

wdrs:describedby

n5:doid.owl

obo:id

DOID:14711

obo:hasDbXref

OMIM:300422 ORDO:323 SNOMEDCT_US_2021_09_01:49984004 MESH:C537923 GARD:2317 OMIM:300581 UMLS_CUI:C0220769 ORDO:93932 OMIM:300321 OMIM:305450 OMIM:300406

obo:hasExactSynonym

Keller syndrome Opitz-Kaveggia syndrome

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_rare_slim

n2:IAO_0000115

A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern.

Subject Item

_:vb50949725

rdf:type

owl:Restriction

owl:onProperty

n2:IDO_0000664

owl:someValuesFrom

n2:GENO_0000149

wdrs:describedby

n5:doid.owl