DISEASES

Disease-gene associations mined from literature

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Human genes for cortisone reductase deficiency

Cortisone reductase deficiency [DOID:0090139]

An endocrine system disease characterized by failure to regenerate the active glucocorticoid cortisol from cortisone resulting in adrenal hyperandrogenism.

Synonyms:  cortisone reductase deficiency,  cortisone reductase deficiencies,  DOID:0090139,  CORTRD,  CORTRDs

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.