petechiae Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Petechiae are pinpoint-sized reddish/purple spots, resembling a rash, that appear just under the skin or a mucous membrane when capillaries have ruptured and some superficial bleeding into the skin has happened. This term refers to an abnormally increased susceptibility to developing petechiae. (Human Phenotype Ontology, HP_0000967)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0000967
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Genes

12 genes associated with the petechiae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ETHE1	ethylmalonic encephalopathy 1
FERMT3	fermitin family member 3
GATA1	GATA binding protein 1 (globin transcription factor 1)
GBA	glucosidase, beta, acid
GP1BA	glycoprotein Ib (platelet), alpha polypeptide
HOXA11	homeobox A11
ITGA2B	integrin, alpha 2b (platelet glycoprotein IIb of IIb/IIIa complex, antigen CD41)
ITGB3	integrin, beta 3 (platelet glycoprotein IIIa, antigen CD61)
OCLN	occludin
PEPD	peptidase D
TREX1	three prime repair exonuclease 1
WAS	Wiskott-Aldrich syndrome