decreased lacrimation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormally decreased lacrimation, that is, reduced ability to produce tears. (Human Phenotype Ontology, HP_0000633)
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12 genes associated with the decreased lacrimation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AAAS achalasia, adrenocortical insufficiency, alacrimia
DST dystonin
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
GMPPA GDP-mannose pyrophosphorylase A
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
PAX1 paired box 1
SETBP1 SET binding protein 1
SOX10 SRY (sex determining region Y)-box 10