Grange Syndrome (GRNG)

Alias:

Arterial Occlusive Disease, Progressive, with Hypertension, Heart Defects, Bone Fragility, and Brachysyndactyly

Grange Occlusive Arterial Syndrome

Grng

Progressive Arterial Occlusive Disease-Hypertension-Heart Defects-Bone Fragility-Brachysyndactyly Syndrome

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

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

Related ID：

MALACARDS：GRN034

OMIM：602531

MESH：D001157