Any congenital disorder of glycosylation in which the cause of the disease is a mutation in FAM20B.
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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
Ehlers-Danlos syndrome, musculocontractural type
MONDO:0011142
temtamy preaxial brachydactyly syndrome
MONDO:0011533
progressive myoclonic epilepsy type 3
MONDO:0012721