ALG10-congenital disorder of glycosylation

MONDO:0100589

Any congenital disorder of glycosylation in which the cause of the disease is a mutation in ALG10.

Also known as: ALG10-CDG, ALG10-congenital disorder of glycosylation

0 clinical trials for this condition and its sub-types, 0 tagged with ALG10-congenital disorder of glycosylation itself.

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