FAM20B-congenital disorder of glycosylation

MONDO:0100588

Any congenital disorder of glycosylation in which the cause of the disease is a mutation in FAM20B.

Also known as: FAM20B-CDG, FAM20B-congenital disorder of glycosylation

0 clinical trials for this condition and its sub-types, 0 tagged with FAM20B-congenital disorder of glycosylation itself.

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