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Hereditary Angioedema Types I and II

"Hereditary Angioedema Types I and II" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information
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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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This graph shows the total number of publications written about "Hereditary Angioedema Types I and II" by people in Harvard Catalyst Profiles by year, and whether "Hereditary Angioedema Types I and II" was a major or minor topic of these publication.
Bar chart showing 7 publications over 5 distinct years, with a maximum of 2 publications in 2017 and 2018
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.