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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)