Diabetes, permanent neonatal, with or without neurologic features

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Diabetes, permanent neonatal, with or without neurologic features
MONDO_0100165
KCNJ11 Unknown
15115830 15292329 15448106 15448107 15580558 15583126 16609879 16670688 16731833 17065345 17213273 17652641 17855752 20022885 24896178 25529582 25678012 27181099 27681997 28842488 28943513
Open Targets
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Diabetes, permanent neonatal, with or without neurologic features.
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Diazoxide-resistant focal hyperinsulinism due to kir6.2 deficiency 1 shared geneKCNJ11 Related via 1 shared gene including KCNJ11. Hyperinsulinemic hypoglycemia, familial, 2 1 shared geneKCNJ11 Related via 1 shared gene including KCNJ11. Dend syndrome 1 shared geneKCNJ11 Related via 1 shared gene including KCNJ11. Congenital hyperinsulinism 1 shared geneKCNJ11 Related via 1 shared gene including KCNJ11. Transient neonatal diabetes mellitus 1 shared geneKCNJ11 Related via 1 shared gene including KCNJ11.