Citrin deficiency

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CITRIN DEFICIENCY, ADOLESCENT OR ADULT ONSET
603471
SLC25A13 Unknown — HPO
CITRIN DEFICIENCY, NEONATAL OR INFANTILE ONSET
605814
SLC25A13 Unknown — HPO, ClinGen
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Citrin deficiency.
5 View disease cluster →
Citrullinemia 1 shared geneSLC25A13 Related via 1 shared gene including SLC25A13. Urea cycle disorder 1 shared geneSLC25A13 Related via 1 shared gene including SLC25A13. Lung cancer 1 shared geneSLC25A13 Related via 1 shared gene including SLC25A13. Osteoarthritis 1 shared geneSLC25A13 Related via 1 shared gene including SLC25A13. Squamous cell carcinoma 1 shared geneSLC25A13 Related via 1 shared gene including SLC25A13.