moderate global developmental delay Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011343
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Genes

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.

Symbol Name
IRX5 iroquois homeobox 5