B3GALT6-congenital disorder of glycosylation

MONDO:0100586

Any congenital disorder of glycosylation in which the cause of the disease is a mutation in B3GALT6.

Also known as: B3GALT6-CDG, B3GALT6-congenital disorder of glycosylation, B3GALT6-related congenital disorder of glycosylation

0 clinical trials for this condition and its sub-types, 0 tagged with B3GALT6-congenital disorder of glycosylation itself.

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Sub-types of B3GALT6-congenital disorder of glycosylation

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