aplasia of the parotid gland Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the parotid gland. (Human Phenotype Ontology, HP_0009740)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009740
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Genes

3 genes associated with the aplasia of the parotid gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3