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Up to: B3GALT6-congenital disorder of glycosylation · Spondyloepimetaphyseal dysplasia with joint laxity
Spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
Any spondyloepimetaphyseal dysplasia with joint laxity in which the cause of the disease is a mutation in the B3GALT6 gene.
This condition has no sub-types.