This HTML5 document contains 64 embedded RDF statements represented using HTML+Microdata notation.

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PrefixNamespace IRI
n5http://caligraph.org/resource/Cartilage%E2%80%93
n17http://caligraph.org/resource/Dominance_(genetics)
n7http://en.wikipedia.org/wiki/Category:
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
n8http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n10http://caligraph.org/ontology/MeSH_code_(C05)
owlhttp://www.w3.org/2002/07/owl#
n14http://caligraph.org/ontology/MeSH_code_(C16)
clgohttp://caligraph.org/ontology/
n12http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C05)
n9http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
dbrhttp://dbpedia.org/resource/
n13http://en.wikipedia.org/wiki/List_of_diseases_(A)
clgrhttp://caligraph.org/resource/
Subject Item
clgr:Spinal_stenosis
clgo:medicalCause
clgr:Achondroplasia
Subject Item
clgr:Achondroplasia
rdf:type
n10: clgo:Cell_surface_receptor_deficiency clgo:Fetal_abnormality n14: clgo:Connective_tissue_disease owl:NamedIndividual clgo:Rare_disease clgo:Growth_disorder
rdfs:label
Achondroplasia
owl:sameAs
dbr:Achondroplasia
prov:wasDerivedFrom
n7:Rare_diseases n8: n9:Mendelian_traits_in_humans n9:Megalencephaly n9:Chromosome_4 n12: n7:Connective_tissue_diseases n13: n9:List_of_fetal_abnormalities n7:Cell_surface_receptor_deficiencies n9:Hypotonia n7:Growth_disorders n9:Fontanelle n9:Cartilage n9:Atelosteogenesis_type_I n9:Skull_bossing n9:Macrocephaly n9:Chondropathy n9:Pseudoachondroplasia
skos:prefLabel
Achondroplasia
skos:altLabel
achondroplastic dwarf Achondroplastic dwarves congenital dwarfism dwarf achondroplastic Achondroplastic dwarfism achondroplasia achondroplasic additional dwarf characteristics achondroplasiac achondroplasia dwarfism
clgo:complications
Ear infections,hyperlordosis,back pain,spinal stenosis,hydrocephalus
clgo:differentialDiagnosis
n5:hair_hypoplasia clgr:Pseudoachondroplasia clgr:Thanatophoric_dysplasia clgr:Hypochondroplasia
clgo:diseasesDB
80
clgo:eMedicineSubject
article
clgo:eMedicineTopic
1258401-overview
clgo:icd10
Q77.4
clgo:icd9
756.4
clgo:medicalCause
clgr:Fibroblast_growth_factor_receptor_3 n17:
clgo:medicalDiagnosis
clgr:Genetic_testing
clgo:medlinePlus
001577
clgo:meshId
D000130
clgo:omim
100800
clgo:orpha
15
clgo:symptom
clgr:Skull_bossing clgr:Macrocephaly
clgo:treatment
clgr:Growth_hormone_therapy clgr:Support_group