|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A moderate delay in the achievement of motor or mental milestones in the domains of development of a child. (Human Phenotype Ontology, HP_0011343)|
|Downloads & Tools|
1 genes associated with the moderate global developmental delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|IRX5||iroquois homeobox 5|