Klippel-Feil Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A physical disorder that has_material_basis_in abnormal segmentation of the vertebra during fetal development which results_in fusion located_in cervical vertebra. (Human Disease Ontology, DOID_10426)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D007714
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Genes

1 genes/proteins associated with the disease Klippel-Feil Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
GDF6 growth differentiation factor 6 2.88009