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Summary Literature (0)
DOID:10426 - Klippel-Feil syndrome

Disease Ontology Definition:A physical disorder that has_material_basis_in 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,

Echinobase Genes :

OMIM:118100 - klippel-feil syndrome 1, autosomal dominant; kfs1
OMIM:613702 - klippel-feil syndrome 3, autosomal dominant; kfs3

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)