mild global developmental delay Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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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.

Symbol Name
ACTB actin, beta
RBBP8 retinoblastoma binding protein 8
RNF168 ring finger protein 168, E3 ubiquitin protein ligase