chilblain lesions Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Chilblains are acral ulcers. (Human Phenotype Ontology, HP_0009710)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009710
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Genes

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

Symbol Name
SAMHD1 SAM domain and HD domain 1
TREX1 three prime repair exonuclease 1