ornithine carbamoyltransferase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Ornithine carbamoyltransferase deficiency
OTC Causal
9143919 3170748 2474822 7951259 1671317 10502831 8956045 10070627 7474905 8081398 9286441 8112735 1721894 8019569 2347583 8081373 8530002 1480464 9065786 10737985 9452024 8830175 2556444 9266388 9452065 8956038 11793483 8807340 8099056 9452049
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with ornithine carbamoyltransferase deficiency.
5 View disease cluster →
Urea cycle disorder 1 shared geneOTC Related via 1 shared gene including OTC. Hyperammonemia 1 shared geneOTC Related via 1 shared gene including OTC. Brain disease 1 shared geneOTC Related via 1 shared gene including OTC. Cognition disorder 1 shared geneOTC Related via 1 shared gene including OTC. Delirium, dementia, and cognitive disorders 1 shared geneOTC Related via 1 shared gene including OTC.