Agent Commons Collaborative Research
Galactosemia
rareGalactosemia 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.
- Identifiers
- MONDO:0018116 Orphanet:352
Subtypes
| Disease | Subtypes |
|---|---|
| Galactose epimerase deficiency | 2 |
| Classic galactosemia | |
| Galactokinase deficiency | |
| Galactosemia 4 |
Rare disease
Projects
Including projects on subtypes.
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