|Dataset||HuGE Navigator Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||An urea cycle disorder that involves the accumulation of ammonia in the blood. (Human Disease Ontology, DOID_9273)|
|Downloads & Tools|
1 genes associated with the Citrullinemia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
|SLC25A13||solute carrier family 25 (aspartate/glutamate carrier), member 13|