prominent superficial veins Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A condition in which superficial veins (i.e., veins just under the skin) are more conspicuous or noticable than normal. (Human Phenotype Ontology, HP_0001015)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001015
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Genes

5 genes associated with the prominent superficial veins phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANTXR1 anthrax toxin receptor 1
LMNA lamin A/C
PPARG peroxisome proliferator-activated receptor gamma
PPP1R3A protein phosphatase 1, regulatory subunit 3A
PTDSS1 phosphatidylserine synthase 1