Ornithine carbamoyltransferase deficiency Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase. (Human Disease Ontology, DOID_9271)
External Link http://www.omim.org/entry/311250
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Genes

1 genes associated with the Ornithine carbamoyltransferase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
OTC ornithine carbamoyltransferase