steatocystoma multiplex Gene Set

Dataset OMIM 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://www.omim.org/entry/184500
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Genes

1 genes associated with the steatocystoma multiplex phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KRT17 keratin 17, type I