60 - autosomal dominant disorders

Achondroplasia

Antithrombin III deficiency

C1 esterase inhibitor deficiency

Ehlers-Danlos syndrome

Familial hypercholesterolaemia

Gilbert's disease

hereditary haemorrhagic telangiectasia

hereditary elliptocysis,

hereditary spherocytosis

Huntington's disease

idiopathic hypoparathyroidism

intestinal polyposis

marble bone disease

Marfan's syndrome

neurofibromatosis

Peutz Jegher’s syndrome

polycystic kidney disease (adult)

protein C deficiency

osteogenesis imperfecta

Treacher Collins syndrome

Tuberous sclerosis

Von Willebrand's disease