Citrullinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An urea cycle disorder that involves the accumulation of ammonia in the blood. (Human Disease Ontology, DOID_9273)
External Link https://www.disgenet.org/browser/0/1/0/C4721769
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Genes

7 genes associated with the disease Citrullinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AASS aminoadipate-semialdehyde synthase
ARSD arylsulfatase D
ASS1 argininosuccinate synthase 1
OTC ornithine carbamoyltransferase
PRMT7 protein arginine methyltransferase 7
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SLC25A33 solute carrier family 25 (pyrimidine nucleotide carrier), member 33