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GENATLAS PHENOTYPE

last update : 26/09/2005

Symbol	CAMT
Location	1p34.2
Name	congenital amegakaryocytic thrombocytopenia
Corresponding gene	MPL
Main clinical features	potentially preleukemic condition
Genetic determination	autosomal dominant
Function/system disorder	hematology
Type	disease

Gene product

Name	thrombopoietin receptor (MPL)

Remark(s)