Any congenital disorder of glycosylation in which the cause of the disease is a mutation in B3GALT6.
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congenital disorder of glycosylation type I
MONDO:0005500
congenital disorder of glycosylation type II
MONDO:0005501
Larsen-like syndrome, B3GAT3 type
MONDO:0009511
spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures
MONDO:0010075
Ehlers-Danlos syndrome, musculocontractural type
MONDO:0011142
temtamy preaxial brachydactyly syndrome
MONDO:0011533