|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
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.