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.
See also reference (FX) in Slovak
proteín inhibujúci komplement C1
See also reference (FX) in English
Complement C1 Inhibitor Protein
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(11) - ARTICLES
(1) - MeSH descriptor
(1) - CiBaMed
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