DISEASES

Disease-gene associations mined from literature

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Human genes for Holt-Oram syndrome

Holt-Oram syndrome [DOID:0060468]

A syndrome characterized by congenital anomalies located_in heart and located_in upper limb.

Synonyms:  Holt-Oram syndrome,  DOID:0060468,  HoltOram syndrome,  Holt-Oram disease,  Holt-Oram disorder ...

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.