abnormality of the vasculature of the conjunctiva Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Any abnormality of the blood vessels of the conjunctiva. (Human Phenotype Ontology, HP_0008054)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0008054
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Genes

13 genes associated with the abnormality of the vasculature of the conjunctiva phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ACVRL1	activin A receptor type II-like 1
ATM	ATM serine/threonine kinase
CTSA	cathepsin A
ENG	endoglin
FUCA1	fucosidase, alpha-L- 1, tissue
GDF2	growth differentiation factor 2
GLA	galactosidase, alpha
GNAQ	guanine nucleotide binding protein (G protein), q polypeptide
MANBA	mannosidase, beta A, lysosomal
MASP1	mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
PCNA	proliferating cell nuclear antigen
SETX	senataxin
SMAD4	SMAD family member 4