|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A mild delay in the achievement of motor or mental milestones in the domains of development of a child. (Human Phenotype Ontology, HP_0011342)|
|Downloads & Tools|
3 genes associated with the mild global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.