DISEASES

Disease-gene associations mined from literature

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Human genes for Holzgreve-Wagner-Rehder Syndrome

Holzgreve-Wagner-Rehder Syndrome [DOID:0060566]

A syndrome characterized by Potter sequence, heart defect, cleft palate, polydactyly, and skeletal defects.

Synonyms:  Holzgreve-Wagner-Rehder Syndrome,  DOID:0060566,  HolzgreveWagnerRehder Syndrome,  Holzgreve-Wagner-Rehder disease,  Holzgreve-Wagner-Rehder 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.