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Hereditary angioedema with C1Inh deficiency
Forms of hereditary angioedema that occur due to mutations in the gene for complement C1 inhibitor protein. Type I hereditary angioedema is associated with reduced serum levels of complement C1 inhibitor protein. Type II hereditary angioedema is associated with the production of a non-functional complement C1 inhibitor protein.
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Hereditary angioedema type 1 26 trials
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Hereditary angioedema type 2 26 trials