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Up to: B3GALT6-congenital disorder of glycosylation · Ehlers-Danlos syndrome, spondylodysplastic type
Ehlers-Danlos syndrome, spondylodysplastic type, 2
Any Ehlers-Danlos syndrome, spondylodysplastic type in which the cause of the disease is a mutation in the B3GALT6 gene.
This condition has no sub-types.