DISEASES

Disease-gene associations mined from literature

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Human genes for cranioectodermal dysplasia

Cranioectodermal dysplasia [DOID:0050577]

A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.

Synonyms:  cranioectodermal dysplasia,  cranioectodermal dysplasias,  DOID:0050577,  Levin syndrome,  Sensenbrenner syndrome ...

Linkouts:  OMIM #1 #2 #3 #4

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.