Classic galactosemia

Disease Export to PDF
Name:
Classic galactosemia
Description:
A life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease.
ORPHAcode:
79239
Synonyms:
GALT deficiency
Galactose-1-phosphate uridyltransferase deficiency
Galactosemia type 1
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14