nasolacrimal duct obstruction Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	any impediment or blockage of the paired channels leading from the lacrimal sacs to the inferior meatus of the nose, through which tears are conducted through the nasal cavity; may be either congenital or acquired; obstruction of the nasolacrimal duct leads to the excess overflow of tears called epiphora (Mammalian Phenotype Ontology, MP_0013451)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000579
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Genes

13 genes associated with the nasolacrimal duct obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CD151	CD151 molecule (Raph blood group)
CREBBP	CREB binding protein
EYA1	EYA transcriptional coactivator and phosphatase 1
FGF10	fibroblast growth factor 10
FGFR2	fibroblast growth factor receptor 2
FGFR3	fibroblast growth factor receptor 3
FREM1	FRAS1 related extracellular matrix 1
NOP10	NOP10 ribonucleoprotein
PAX1	paired box 1
PTDSS1	phosphatidylserine synthase 1
TCOF1	Treacher Collins-Franceschetti syndrome 1
TFAP2A	transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63	tumor protein p63