expressive language delay Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A delay in the acquisition of the ability to use language to communicate needs, wishes, or thoughts. (Human Phenotype Ontology, HP_0002474)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002474
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Genes

2 genes associated with the expressive language delay phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NSD1 nuclear receptor binding SET domain protein 1
SRCAP Snf2-related CREBBP activator protein