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Related to glycogen-storage disease: glycogen storage disease Ib


n. pl. gly·co·ge·no·ses (-sēz′)
References in periodicals archive ?
The African origin of the common mutation in African American patients with glycogen-storage disease type II.
Molecular genetics of glycogen-storage disease type 1a in Chinese patients of Taiwan.
Conversely, he cites genetic diseases frequently found among Sephardic Jewish, Arab and other Mediterranean people--such as Mediterranean fever, glucose-6-phosphate dehydrogenate deficiency and Type III glycogen-storage disease as being rare among the Ashkenazi.