Steatocystoma Multiplex Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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 https://www.disgenet.org/browser/0/1/0/C0259771
Similar Terms
Downloads & Tools

Genes

3 genes associated with the disease Steatocystoma Multiplex in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOB apolipoprotein B
KRT17 keratin 17, type I
KRT6B keratin 6B, type II