transient neonatal diabetes mellitus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A neonatal diabetes mellitus characterized by hyperglycemia during the neonatal period that remits during infancy but recurs in later life in most patients. (Human Disease Ontology, DOID_0060334)
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3 genes associated with the transient neonatal diabetes mellitus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
ZFP57 ZFP57 zinc finger protein