facial erythema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Redness of the skin of the face, caused by hyperemia of the capillaries in the lower layers of the skin. (Human Phenotype Ontology, HP_0001041)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001041
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Genes

3 genes associated with the facial erythema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
MBTPS2 membrane-bound transcription factor peptidase, site 2
SAT1 spermidine/spermine N1-acetyltransferase 1