Citrin deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CITRIN DEFICIENCY
C1997910MONDO:0016602
SLC25A13 Causal
10369257 10642534 11343052 11343053 11566871 14701727 18367750 18392553 19036621 21914561 24586645 31607264
ClinGen, Disgenet, GWAS catalog
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.