Galactose-1-phosphate uridyltransferase deficiency (Q40044)
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Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C51.40 |
||
| English | Galactose-1-phosphate uridyltransferase deficiency |
Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease. |
