|Dataset||DISEASES Curated Gene-Disease Assocation Evidence Scores|
|Category||disease or phenotype associations|
|Description||An urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase. (Human Disease Ontology, DOID_9271)|
|Downloads & Tools|
1 genes involed in the disease ornithine carbamoyltransferase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.