DISEASES

Disease-gene associations mined from literature

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Human genes for citrullinemia

Citrullinemia [DOID:9273]

An inherited urea cycle disorder that involves the accumulation of ammonia and other toxic substances in the blood.

Synonyms:  citrullinemia,  citrullinemias,  DOID:9273,  ASS deficiency,  deficiency of citrulline-aspartate ligase ...

Linkouts:  OMIM #1 #2 #3

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.