DISEASES

Disease-gene associations mined from literature

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Human genes for short chain acyl-CoA dehydrogenase deficiency

Short chain acyl-CoA dehydrogenase deficiency [DOID:0080154]

A lipid metabolism disorder that is characterized by deficiency of the enzyme short chain acyl-CoA dehydrogenase that results in the inability to convert short chain fatty acids.

Synonyms:  short chain acyl-CoA dehydrogenase deficiency,  DOID:0080154,  short chain acylCoA dehydrogenase deficiency,  short chain acyl-CoA dehydrogenase deficiencies

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.