DISEASES

Disease-gene associations mined from literature

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Human genes for pyrimidine metabolic disorder

Pyrimidine metabolic disorder [DOID:0050832]

An inherited metabolic disorder involving dysfunction of pyrimidine metabolism.

Synonyms:  pyrimidine metabolic disorder,  DOID:0050832,  pyrimidine metabolic disease,  pyrimidine metabolic syndrome,  pyrimidine metabolic disorders

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.