DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Froelich syndrome

Froelich syndrome [DOID:6676]

A hypothalamic disease that is characterized by endocrine dysfunction of the hypothalamic gland resulting in delayed puberty, small testes, and obesity.

Synonyms:  Froelich syndrome,  DOID:6676,  Froelich disease,  Froelich disorder,  Froelich syndromes ...

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.