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
Similar Terms
Downloads & Tools


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