nevus flammeus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A congenital vascular malformation consisting of superficial and deep dilated capillaries in the skin which produce a reddish to purplish discolouration of the skin. (Human Phenotype Ontology, HP_0001052)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001052
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Genes

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

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
GNAQ guanine nucleotide binding protein (G protein), q polypeptide
RBM8A RNA binding motif protein 8A
ROR2 receptor tyrosine kinase-like orphan receptor 2
WNT5A wingless-type MMTV integration site family, member 5A