Inosine triphosphate pyrophosphohydrolase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Inosine triphosphatase deficiency
MONDO_0013461
ITPA Causal
27604308
Open Targets
Inosine triphosphate pyrophosphohydrolase deficiency
MONDO_0013461
ITPA Unknown
12384777 12436200
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Inosine triphosphate pyrophosphohydrolase deficiency.
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Epileptic encephalopathy, early infantile, 35 1 shared geneITPA Related via 1 shared gene including ITPA. Corneal dystrophy 1 shared geneITPA Related via 1 shared gene including ITPA. Genetic developmental and epileptic encephalopathy 1 shared geneITPA Related via 1 shared gene including ITPA. Hemolytic anemia 1 shared geneITPA Related via 1 shared gene including ITPA. Anemia 1 shared geneITPA Related via 1 shared gene including ITPA.