ALG12, ALG12 alpha-1,6-mannosyltransferase, 79087

N. diseases: 49; N. variants: 12
Disease: Congenital disorder of glycosylation type 1G ×
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C2931001
Disease: Congenital disorder of glycosylation type 1G
Congenital disorder of glycosylation type 1G 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases Disease or Syndrome 1 10 0.710 None 1.000 7 10 2002 2016