ornithine carbamoyltransferase deficiency Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description An urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase. (Human Disease Ontology, DOID_9271)
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Genes

1 genes involed in the disease ornithine carbamoyltransferase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
OTC ornithine carbamoyltransferase