developmental stagnation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A cessation of the development of a child in the areas of motor skills, speech and language, cognitive skills, and social and/or emotional skills. (Human Phenotype Ontology, HP_0007281)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007281
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Genes

4 genes associated with the developmental stagnation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GLB1 galactosidase, beta 1
MCOLN1 mucolipin 1
NUP62 nucleoporin 62kDa
ST3GAL5 ST3 beta-galactoside alpha-2,3-sialyltransferase 5