DISEASES

Disease-gene associations mined from literature

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Human genes for thiamine deficiency disease

Thiamine deficiency disease [DOID:0070313]

A nutritional deficiency disease that is characterized by low levels of thiamine.

Synonyms:  thiamine deficiency disease,  DOID:0070313,  thiamine deficiency disorder,  thiamine deficiency syndrome,  thiamine deficiency diseases

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.