 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.
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.
| Descriptor ID |
D056829
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| MeSH Number(s) |
C14.907.079.500.750 C17.800.862.945.066.500.750 C20.543.480.904.066.500.750
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| Concept/Terms |
Hereditary Angioedema Types I and II- Hereditary Angioedema Types I and II
- Deficiency of C1 Esterase Inhibitor
- Angioedema, Hereditary, Types I and II
- C1 Esterase Inhibitor, Deficiency Of
- Hereditary Angioedema Type 1
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Below are MeSH descriptors whose meaning is more general than "Hereditary Angioedema Types I and II".
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This graph shows the total number of publications written about "Hereditary Angioedema Types I and II" by people in this website by year, and whether "Hereditary Angioedema Types I and II" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hereditary Angioedema Types I and II" by people in Profiles.
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Zuraw BL, Bernstein JA, Lang DM, Craig T, Dreyfus D, Hsieh F, Khan D, Sheikh J, Weldon D, Bernstein DI, Blessing-Moore J, Cox L, Nicklas RA, Oppenheimer J, Portnoy JM, Randolph CR, Schuller DE, Spector SL, Tilles SA, Wallace D. A focused parameter update: hereditary angioedema, acquired C1 inhibitor deficiency, and angiotensin-converting enzyme inhibitor-associated angioedema. J Allergy Clin Immunol. 2013 Jun; 131(6):1491-3.
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