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About:
clgr:
Klippel–Feil_syndrome
Property
Value
rdf:
type
Orthopaedic eponyms
owl:
NamedIndividual
Neurological condition or disorder
Rare syndrome
Skin condition
Genodermatose
Congenital disorder of musculoskeletal system
ICD-9 codes 740–759: congenital anomaly
MeSH code (C16)
MeSH code (C05)
rdfs:
label
Klippel–Feil syndrome
owl:
sameAs
dbr:
Klippel–Feil_syndrome
prov:
wasDerivedFrom
http://en.wikipedia.org/wiki/Category:Genodermatoses
http://en.wikipedia.org/wiki/List_of_orthopaedic_eponyms
http://en.wikipedia.org/wiki/List_of_diseases_(K)
http://en.wikipedia.org/wiki/List_of_neurological_conditions_and_disorders
http://en.wikipedia.org/wiki/List_of_skin_conditions
http://en.wikipedia.org/wiki/List_of_syndromes
http://en.wikipedia.org/wiki/Category:Rare_syndromes
http://en.wikipedia.org/wiki/Congenital_mirror_movement_disorder
http://en.wikipedia.org/wiki/Webbed_toes
http://en.wikipedia.org/wiki/Category:Congenital_disorders_of_musculoskeletal_system
http://en.wikipedia.org/wiki/List_of_ICD-9_codes_740%E2%80%93759:_congenital_anomalies
http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C16)
http://en.wikipedia.org/wiki/Sprengel's_deformity
http://en.wikipedia.org/wiki/Tethered_spinal_cord_syndrome
http://en.wikipedia.org/wiki/List_of_MeSH_codes_(C05)
http://en.wikipedia.org/wiki/Wildervanck_syndrome
skos:
prefLabel
Klippel–Feil syndrome
skos:
altLabel
:Klippel–Feil syndrome
Klippel-Feil Syndrome
Klippel-Feil malformation
Klippel-Feil syndrome
Klippel–Feil syndrome recessive type
clgo:
diseasesDB
7197
clgo:
eMedicineSubject
orthoped
clgo:
eMedicineTopic
408
clgo:
icd10
Q76.1
clgo:
icd9
756.16
clgo:
medicalCause
Mutation
clgo:
meshId
D007714
clgo:
omim
118100
clgo:
symptom
Spina bifida
Congenital heart defect
Scoliosis
clgo:
medicalSpecialty
Orthopedic surgery
Pediatrics
is
clgo:
differentialDiagnosis
of
Srb's anomaly
Iniencephaly
is
clgo:
knownFor
of
Maurice Klippel