citrullinemia Gene Set

Dataset DISEASES Text-mining Gene-Disease Association Evidence Scores
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)
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Genes

5 genes co-occuring with the disease citrullinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
ASS1 argininosuccinate synthase 1 2.30707
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13 1.60681
ASL argininosuccinate lyase 1.19834
OTC ornithine carbamoyltransferase 0.955779
BECN1 beclin 1, autophagy related 0.670732