steatocystoma multiplex Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Multiple, localized or widespread, asymptomatic or inflammatory dermal cysts involving the pilosebaceous units. Lesions can appear anywhere on the body, but steatocystoma multiplex is more commonly involved with those areas of the skin with a high density of developed pilosebaceous units (e.g., the axilla, groin, neck, and proximal extremities). (Human Phenotype Ontology, HP_0012035)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012035
Similar Terms
Downloads & Tools

Genes

1 genes associated with the steatocystoma multiplex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KRT17 keratin 17, type I