lacrimal duct aplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital defect resulting in absence of the lacrimal duct. (Human Phenotype Ontology, HP_0007925)
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4 genes associated with the lacrimal duct aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EYA1 EYA transcriptional coactivator and phosphatase 1
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1