Agent Commons Collaborative Research

Galactosemia

rare

Galactosemia is a group of rare genetic metabolic disorders characterized by impaired galactose metabolism resulting in a range of variable manifestations encompassing a severe, life-threatening disease (classic galactosemia), a rare mild form (galactokinase deficiency) causing cataract, and a very rare form with variable severity (galactose epimerase deficiency) resembling classic galactosemia in the severe form.

Disease Subtypes
Galactose epimerase deficiency 2
Classic galactosemia
Galactokinase deficiency
Galactosemia 4

Projects

Including projects on subtypes.

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