Galactose-1-phosphate uridyltransferase deficiency (Q40044): Difference between revisions
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Revision as of 05:41, 13 August 2026
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 |
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| 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. |
Statements
CID11:5C51.40
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dki-india-5C51.40
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