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Summary Literature (1)
DOID:10426 - Klippel-Feil syndrome

Disease Ontology Definition:A physical disorder that is characterized by abnormal segmentation of the vertebra during fetal development which results in fusion located in cervical vertebra.

Synonyms: Klippel-Feil and Turner syndrome, Klippel-Feil deformity, deafness and facial asymmetry, autosomal dominant Klippel-Feil syndrome, congenital dystrophia brevicollis, congenital synostosis of cervical vertebrae,

Xenbase Genes : gdf3, myo18b, gdf6

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0001029 - Klippel-Feil syndrome

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): physical disorder (is_a), spinal disease (is_a), syndrome (is_a)