lacrimal gland aplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital defect of development characterized by absence of the lacrimal gland. (Human Phenotype Ontology, HP_0007656)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007656
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Genes

3 genes associated with the lacrimal gland aplasia 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