Mutations in this gene have been shown to cause developmental disorders such as Spondyloepimetaphyseal dysplasia with joint laxity.
It is due to mutations in the Bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthetase 2 (PAPSS2) gene which is located on the long arm of chromosome 10 (10q22-q24).
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Spondyloepimetaphyseal dysplasia, Pakistani type is a form of spondyloepimetaphyseal dysplasia involving PAPSS2 (also known as "ATPSK2").
Thanatophoric dysplasia | thanatophoric dysplasia | Spondyloepimetaphyseal dysplasia | spondyloepimetaphyseal dysplasia | Hip dysplasia (human) | Hip dysplasia (disambiguation) | Hip dysplasia | hip dysplasia | Fibromuscular Dysplasia Society of America | Fibromuscular dysplasia |