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bn:01245626n
Noun Concept
Categories: Articles with short description, Rare syndromes, Genodermatoses, Congenital disorders of musculoskeletal system
EN
Klippel-Feil syndrome  Klippel–Feil syndrome  Andre Feil  autosomal dominant Klippel-Feil syndrome  Cervical vertebral fusion
EN
Klippel–Feil syndrome, also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any two of the seven bones in the neck. Wikipedia
Definitions
Relations
Sources
EN
Klippel–Feil syndrome, also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any two of the seven bones in the neck. Wikipedia
A rare congenital condition Wikipedia Disambiguation
Physical disorder that has material basis in abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra Wikidata
IS A
rare disease
birth defect
syndrome
dorsopathy
HAS KIND
Wildervanck syndrome
ANATOMICAL LOCATION
spinal curvature
GENETIC ASSOCIATION
GDF3
GDF6
MEOX1
HEALTH SPECIALTY
medical genetics
NAMED AFTER
Maurice Klippel
Wikipedia
EN
Klippel–Feil syndrome
Wikidata
EN
Klippel-Feil syndrome
Wikipedia Redirections
EN
Andre Feil, cervical vertebral fusion, Cervical vertebral fusion, congenital, Congenital cervical vertebral fusion, Congenital fused cervical segments, Feil-Klippel syndrome, Frontonasal dysplasia Klippel-Feil syndrome, Frontonasal dysplasia klippel feil syndrome, Frontonasal dysplasia Klippel–Feil syndrome, Fused cervical segments, congenital, Klippel-Feil anomalad, Klippel-Feil anomaly, Klippel-Feil deformity, Klippel-Feil malformation, Klippel-Feil phenotype, Klippel-Feil sequence, Klippel-Feil syndrome, Klippel-Feil Syndrome, Klippel-feil syndrome, Klippel-Feil syndrome dominant type, Klippel-Feil syndrome recessive type, Klippel Feil, Klippel Feil syndrome, Klippel Feil Syndrome, Klippel Feil syndrome dominant type, Klippel Feil syndrome recessive type, Klippel–Feil Syndrome, Klippel–Feil syndrome dominant type, Klippel–Feil syndrome recessive type, Short neck syndrome
Wikidata Alias
EN
autosomal dominant Klippel-Feil syndrome, Cervical vertebral fusion, congenital dystrophia brevicollis, congenital synostosis of cervical vertebrae, Klippel-Feil and Turner syndrome, Klippel-Feil deformity, deafness and facial asymmetry, Klippel Feil syndrome

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