Grange Syndrome (GRNG)

Grange Syndrome, also known as arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly, is related to learning disability and chromosome 2q35 duplication syndrome. An important gene associated with Grange Syndrome is YY1AP1 (YY1 Associated Protein 1). Affiliated tissues include heart and bone, and related phenotypes are specific learning disability and arterial stenosis