DISEASES

Disease-gene associations mined from literature

Human genes for Klippel-Feil syndrome

Klippel-Feil syndrome [DOID:10426]

A congenital disorder that has_material_basis_in abnormal segementation of the vertebra during fetal development which results_in fusion located_in cervical vertebra.

Synonyms:  Klippel-Feil syndrome,  DOID:10426,  KlippelFeil syndrome,  Klippel-Feil disease,  Klippel-Feil disorder ...

Linkouts:  OMIM #1 #2 #3