carbamoyl phosphate synthetase i deficiency disease Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An amino acid metabolic disorder that involves accumulation of ammonia in the blood. (Human Disease Ontology, DOID_9280)
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Genes

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

Symbol Name Standardized Value
CPS1 carbamoyl-phosphate synthase 1, mitochondrial 2.4959
OTC ornithine carbamoyltransferase 1.80201
NAGS N-acetylglutamate synthase 1.46495
ROM1 retinal outer segment membrane protein 1 1.17078
HMOX2 heme oxygenase 2 1.08495