This HTML5 document contains 41 embedded RDF statements represented using HTML+Microdata notation.

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PrefixNamespace IRI
n14http://en.wikipedia.org/wiki/Cole%E2%80%93
n10http://en.wikipedia.org/wiki/Category:
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
n5http://en.wikipedia.org/wiki/Saethre%E2%80%93
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n11http://en.wikipedia.org/wiki/List_of_diseases_(P)
owlhttp://www.w3.org/2002/07/owl#
clgohttp://caligraph.org/ontology/
n6http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
dbrhttp://dbpedia.org/resource/
n12http://en.wikipedia.org/wiki/List_of_diseases_(M)
clgrhttp://caligraph.org/resource/
Subject Item
clgr:Pfeiffer_syndrome
rdf:type
clgo:Skin_condition clgo:Congenital_disorder clgo:Syndrome_with_dysmelia owl:NamedIndividual clgo:Rare_syndrome clgo:Cell_surface_receptor_deficiency
rdfs:label
Pfeiffer syndrome
owl:sameAs
dbr:Pfeiffer_syndrome
prov:wasDerivedFrom
n5:Chotzen_syndrome n6:List_of_syndromes n6:Exophthalmos n6:List_of_congenital_disorders n10:Cell_surface_receptor_deficiencies n11: n12: n6:Fibroblast_growth_factor_receptor_2 n10:Rare_syndromes n6:Chromosome_10 n10:Congenital_disorders n6:The_Resilience_Project n6:Webbed_toes n6:Chromosome_8 n14:Carpenter_syndrome n6:List_of_skin_conditions n10:Syndromes_with_dysmelia n6:Dysmelia n6:Craniosynostosis n6:Skull_bossing n6:Acrocephalosyndactyly
skos:prefLabel
Pfeiffer syndrome
skos:altLabel
Pfeiffer syndrome type 2 Pfeiffer type acrocephalosyndactyly Pfeiffer Syndrome Mesomelic syndrome Pfeiffer type
clgo:diseasesDB
32145
clgo:icd10
Q87.0
clgo:icd9
755.55
clgo:medicalCause
clgr:Genetics
clgo:meshId
D000168
clgo:omim
101600
clgo:orpha
710