DISEASES

Disease-gene associations mined from literature

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Human genes for Klippel-Feil syndrome

Klippel-Feil syndrome [DOID:10426]

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

Linkouts:  OMIM #1 #2 #3

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.