<https://averbis.com/icd_10_cm_2017/e74-21-classical-galactosemia-heterozygous-type-disorder/#webpage>
<http://schema.org/description>
"Classical galactosaemia|Classical galactosaemia, heterozygous type|Classical galactosaemia, homozygous Duarte-type|Classical galactosaemia, homozygous Negro-type|Classical galactosemia|Classical galactosemia, heterozygous type|Classical galactosemia, heterozygous type (disorder)|Classical galactosemia, homozygous Duarte-type|Classical galactosemia, homozygous Duarte-type (disorder)|Classical galactosemia, homozygous Negro-type|Classical galactosemia, homozygous Negro-type (disorder)|Deficiency of UDPglucose-hexose-1-phosphate uridylyltransferase|Deficiency of galactose-1-phosphate uridyl transferase|Deficiency of hexose-1-phosphate uridylyltransferase|Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase|Deficiency of uridine diphosphate-glucose-hexose-1-phosphate uridylyltransferase (disorder)|Deficiency of uridyl transferase|Epimerase deficiency|Erythrocyte uridine diphosphate galactose-4-epimerase deficiency|Erythrocyte uridine diphosphate galactose-4-epimerase deficiency (disorder)|GALE|GALT deficiency|Galactosaemia|Galactosaemia - epimerase deficiency|Galactosaemia III|Galactose epimerase deficiency|Galactosemia (disorder)|Galactosemia - epimerase deficiency|Galactosemia III|Generalised uridine diphosphate galactose-4-epimerase deficiency|Generalized uridine diphosphate galactose-4-epimerase deficiency|Generalized uridine diphosphate galactose-4-epimerase deficiency (disorder)|Perinatal jaundice due to galactosaemia|Perinatal jaundice due to galactosemia|Perinatal jaundice due to galactosemia (disorder)|Transferase deficiency galactosaemia|Transferase deficiency galactosemia|UDPgalactose-4-epimerase deficiency|UDPglucose-4-epimerase deficiency|Uridine diphosphate (UDP) glucose-4-epimerase deficiency|Uridine diphosphate galactose-4 epimerase deficiency|Uridine diphosphate galactose-4-epimerase deficiency|Uridine diphosphate glucose-4-epimerase deficiency|Uridine diphosphate glucose-4-epimerase deficiency (disorder)"
<https://averbis.com/icd_10_cm_2017/e74-21-classical-galactosemia-heterozygous-type-disorder/>