ornithine translocase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
ornithine translocase deficiency
SLC25A15 Unknown — ClinGen
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with ornithine translocase deficiency.
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Citrullinemia 1 shared geneSLC25A15 Related via 1 shared gene including SLC25A15. Urea cycle disorder 1 shared geneSLC25A15 Related via 1 shared gene including SLC25A15. Amino acid metabolism disorder 1 shared geneSLC25A15 Related via 1 shared gene including SLC25A15. Cardiac arrhythmia 1 shared geneSLC25A15 Related via 1 shared gene including SLC25A15. Intellectual developmental disorder 1 shared geneSLC25A15 Related via 1 shared gene including SLC25A15.