This HTML5 document contains 31 embedded RDF statements represented using HTML+Microdata notation.

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PrefixNamespace IRI
n2http://caligraph.org/resource/Cartilage%E2%80%93
skoshttp://www.w3.org/2004/02/skos/core#
rdfshttp://www.w3.org/2000/01/rdf-schema#
n5http://en.wikipedia.org/wiki/Category:
n9http://en.wikipedia.org/wiki/Hirschsprung'
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n11http://dbpedia.org/resource/Cartilage%E2%80%93
n12http://en.wikipedia.org/wiki/List_of_diseases_(C)
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#
clgrhttp://caligraph.org/resource/
Subject Item
n2:hair_hypoplasia
rdf:type
clgo:Autosomal_recessive_disorder clgo:Skin_condition clgo:Noninfectious_immunodeficiency-related_cutaneous_condition owl:NamedIndividual clgo:Rare_genetic_syndrome clgo:Radiographic_finding_associated_with_cutaneous_conditions clgo:Primary_immunodeficiency clgo:Genodermatose
rdfs:label
Cartilage–hair hypoplasia
owl:sameAs
n11:hair_hypoplasia
prov:wasDerivedFrom
n5:Rare_genetic_syndromes n6:List_of_radiographic_findings_associated_with_cutaneous_conditions n6:List_of_skin_conditions n9:s_disease n5:Genodermatoses n6:List_of_primary_immunodeficiencies n5:Noninfectious_immunodeficiency-related_cutaneous_conditions n6:Finnish_heritage_disease n12: n5:Autosomal_recessive_disorders
skos:prefLabel
Cartilage–hair hypoplasia
skos:altLabel
Cartilage hair hypoplasia like syndrome Cartilage hair hypoplasia cartilage–hair hypoplasia dwarfism cartilage–hair hypoplasia
clgo:icd10
Q78.8
clgo:meshId
C535916
clgo:omim
250250
clgo:orpha
175
clgo:symptom
clgr:Neutropenia
Subject Item
clgr:Achondroplasia
clgo:differentialDiagnosis
n2:hair_hypoplasia