Category
page 1Serpinopathies
alpha-1-antitrypsin deficiency
genetic disorder that may result in lung disease or liver disease
hereditary angioedema
genetic disease characterized by the occurrence of transitory and recurrent subcutaneous and/or submucosal edemas resulting in swelling and/or abdominal pain
antithrombin III deficiency
inherited blood coagulation disease characterized by the tendency to form clots in the veins