Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 08-06-2018

Symbol	STM
Location	17q21.2
Name	steatocystoma multiplex
Corresponding gene	KRT17
Main clinical features	round or oval cystic tumors widely distributed on the back, anterior trunk, arms, scrotum, and thighs, especially the cysts in exposed areas of the body, created serious self-image problems
Genetic determination	autosomal dominant
Function/system disorder	dermatology
Type	disease

Remark(s)

association of steatocystoma multiplex with pachyonychia congenita may represent a distinct mutation distinct