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GENATLAS PHENOTYPE

last update : 15-07-2013

Symbol	IMF2
Location	19p13
Name	infantile myofibromatosis-2
Corresponding gene	NOTCH3
Main clinical features	disorder of mesenchymal proliferation characterized by the development of benign tumors in the skin, muscle, bone, and viscera soft tissue lesions may regress spontaneously
Genetic determination
Function/system disorder
Type	disease

Remark(s)