periorbital fullness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Increase in periorbital soft tissue. (Human Phenotype Ontology, HP_0000629)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000629
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Genes

7 genes associated with the periorbital fullness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DOCK7 dedicator of cytokinesis 7
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
NRAS neuroblastoma RAS viral (v-ras) oncogene homolog
TWIST2 twist family bHLH transcription factor 2