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GENATLAS PHENOTYPE

last update : 05-07-2013

Symbol	FMST
Location	4q12
Name	mastocytosis
Corresponding gene	KIT
Main clinical features	urticaria pigmentosa and cutaneous mastocytosis, bullous mastocytosis with associated hematologic conditions or urticaria pigmentosa (somatic mutations of KIT in peripheral blood mononuclear cells)
Genetic determination	autosomal dominant
Function/system disorder	dermatology
Type	malignancy

Remark(s)