DISEASES

Disease-gene associations mined from literature

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Human genes for Cornelia de Lange syndrome

Cornelia de Lange syndrome [DOID:11725]

A syndrome that is characterized by slow growth before and after birth, intellectual disability that is usually severe to profound, skeletal abnormalities involving the arms and hands, and distinctive facial features.

Synonyms:  Cornelia de Lange syndrome,  Cornelia de Lange disease,  Cornelia de Lange disorder,  Cornelia de Lange syndromes,  DOID:11725 ...

Linkouts:  OMIM #1 #2 #3 #4 #5

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.