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Q34789899-CA2BF5F3-CA05-4975-BE75-A53E9E327544
Q34789899-CA2BF5F3-CA05-4975-BE75-A53E9E327544
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34789899-CA2BF5F3-CA05-4975-BE75-A53E9E327544
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.
P921
Q34789899-CA2BF5F3-CA05-4975-BE75-A53E9E327544
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34789899-CA2BF5F3-CA05-4975-BE75-A53E9E327544
rank
NormalRank
type
BestRank
Statement
P921
congenital disorder of glycosylation type IId