papule Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A circumscribed, solid elevation of skin with no visible fluid, varying in size from a pinhead to less than 10mm in diameter at the widest point. (Human Phenotype Ontology, HP_0200034)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0200034
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Genes

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

Symbol Name
ERCC4 excision repair cross-complementation group 4
NOD2 nucleotide-binding oligomerization domain containing 2