Inborn disorder in which the enzyme galactose-1-phosphate uridyl transferase, that converts galactose-1-phosphate into glucose-1-phosphate, is absent. Excess galactose-1-phosphate accumulates in the blood and a variety of problems result.
<biochemistry> A rare genetic (autosomal recessive) disorder characterised by the inability a defect in the enzyme (galactose 1 phosphate uridyl transferase) that converts galactose 1 phosphate into glucose 1 phosphate is absent. ... Excess galactose 1 phosphate accumulates in the blood and a variety of problems result. ... Inheritance: autos...Found on http://www.encyclo.co.uk/local/20973
a genetic disorder in which galactose cannot be converted into glucose Found on http://www.medichecks.com/glossary.cfm?ltr=G
No exact match found