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GENATLAS PHENOTYPE

last update : 17-10-2018

Symbol	DSAP1
Location	12q24.1
Name	porokeratosis, disseminated superficial actinic, 1
Corresponding gene	SART3
Other symbol(s)	PPPD, DSAP
Main clinical features	chronic disorder of keratinization characterized by a cornoid lamella with parakeratosis, hyperkeratosis and loss of granular layers
Genetic determination	autosomal dominant
Related entries	including porokeratosis palmaris et plantaris disseminata, dyskeratotic disorder
Function/system disorder	dermatology
Type	disease

Remark(s)