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GENATLAS PHENOTYPE

last update : 26/09/2005

Symbol	APOA2
Location	1q21-q23
Name	apolipoprotein A-II deficiency
Corresponding gene	APOA2
Main clinical features	systemic amyloidosis hereditary (nephropathy)
Genetic determination
Function/system disorder	metabolism/lipoprotein-lipid
Type	disease

Gene product

Name	apolipoprotein A-II (APOA2)