This HTML5 document contains 17 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_0060383

rdf:type

owl:Class

rdfs:subClassOf

n2:DOID_0060379

rdfs:label

acrofacial dysostosis Rodriguez type

wdrs:describedby

n5:doid.owl

obo:id

DOID:0060383

obo:created_by

elvira

obo:creation_date

2015-09-21T15:30:41Z

obo:hasDbXref

GARD:496 SNOMEDCT_US_2021_09_01:720430002 MESH:C538183 ORDO:1788 UMLS_CUI:C1860119 OMIM:201170

obo:hasExactSynonym

acrofacial dysostosis, syndrome of Rodriguez

obo:hasOBONamespace

disease_ontology

obo:inSubset

n8:DO_rare_slim

n2:IAO_0000115

An acrofacial dysostosis that is characterized by CNS malformations, lung anomalies, congenital heart defects, dysmorphic facies and limb reduction, and has_material_basis_in autosomal recessive inheritance.