Steatocystoma Multiplex Gene Set

Dataset CTD 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 http://ctdbase.org/detail.go?type=disease&acc=MESH:D062685
Similar Terms
Downloads & Tools

Genes

1 genes/proteins associated with the disease Steatocystoma Multiplex from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
KRT17 keratin 17, type I 2.88009