Citrullinemia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An urea cycle disorder that involves the accumulation of ammonia in the blood. (Human Disease Ontology, DOID_9273)
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Genes

1 genes associated with the Citrullinemia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13