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PrefixNamespace IRI
n10http://en.wikipedia.org/wiki/List_of_diseases_(K)
n19http://dbpedia.org/resource/Klippel%E2%80%93
n2http://caligraph.org/resource/Klippel%E2%80%93
n9http://en.wikipedia.org/wiki/Category:
rdfshttp://www.w3.org/2000/01/rdf-schema#
skoshttp://www.w3.org/2004/02/skos/core#
n11http://caligraph.org/resource/Srb'
n20http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
rdfhttp://www.w3.org/1999/02/22-rdf-syntax-ns#
n15http://caligraph.org/ontology/MeSH_code_(C05)
n5http://caligraph.org/ontology/ICD-9_codes_740%E2%80%93759:
n18http://caligraph.org/ontology/MeSH_code_(C16)
owlhttp://www.w3.org/2002/07/owl#
n12http://en.wikipedia.org/wiki/List_of_ICD-9_codes_740%E2%80%93759:
clgohttp://caligraph.org/ontology/
n16http://en.wikipedia.org/wiki/Sprengel'
n14http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C05)
n4http://en.wikipedia.org/wiki/
provhttp://www.w3.org/ns/prov#
xsdhhttp://www.w3.org/2001/XMLSchema#
clgrhttp://caligraph.org/resource/
Subject Item
n11:s_anomaly
clgo:differentialDiagnosis
n2:Feil_syndrome
Subject Item
n2:Feil_syndrome
rdf:type
n5:_congenital_anomaly clgo:Orthopaedic_eponyms clgo:Skin_condition clgo:Neurological_condition_or_disorder owl:NamedIndividual n15: clgo:Genodermatose clgo:Rare_syndrome n18: clgo:Congenital_disorder_of_musculoskeletal_system
rdfs:label
Klippel–Feil syndrome
owl:sameAs
n19:Feil_syndrome
prov:wasDerivedFrom
n4:List_of_skin_conditions n4:Tethered_spinal_cord_syndrome n9:Genodermatoses n10: n12:_congenital_anomalies n14: n16:s_deformity n4:Webbed_toes n4:Wildervanck_syndrome n9:Rare_syndromes n9:Congenital_disorders_of_musculoskeletal_system n4:List_of_orthopaedic_eponyms n4:List_of_neurological_conditions_and_disorders n4:Congenital_mirror_movement_disorder n4:List_of_syndromes n20:
skos:prefLabel
Klippel–Feil syndrome
skos:altLabel
Klippel-Feil malformation Klippel-Feil syndrome :Klippel–Feil syndrome Klippel–Feil syndrome recessive type Klippel-Feil Syndrome
clgo:diseasesDB
7197
clgo:eMedicineSubject
orthoped
clgo:eMedicineTopic
408
clgo:icd10
Q76.1
clgo:icd9
756.16
clgo:medicalCause
clgr:Mutation
clgo:meshId
D007714
clgo:omim
118100
clgo:symptom
clgr:Congenital_heart_defect clgr:Spina_bifida clgr:Scoliosis
clgo:medicalSpecialty
clgr:Pediatrics clgr:Orthopedic_surgery
Subject Item
clgr:Maurice_Klippel
clgo:knownFor
n2:Feil_syndrome
Subject Item
clgr:Iniencephaly
clgo:differentialDiagnosis
n2:Feil_syndrome