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GENATLAS PHENOTYPE

last update : 26/06/2006

Symbol	DPYS
Location	8q22
Name	dihydropyrimidinuria associated
Corresponding gene	DPYS
Main clinical features	variable clinical phenotype
Genetic determination	autosomal recessive
Function/system disorder	endocrinology
Type	disease

Gene product

Name	dihydropyrimidinase (DPYS)