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
|
| MeSH Number(s) |
C14.907.079.500.750 C17.800.862.945.066.500.750 C20.543.480.904.066.500.750
|
| 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
|
Below are MeSH descriptors whose meaning is more general than "Hereditary Angioedema Types I and II".
Below are MeSH descriptors whose meaning is more specific than "Hereditary Angioedema Types I and II".
This graph shows the total number of publications written about "Hereditary Angioedema Types I and II" by people in UAMS Profiles by year, and whether "Hereditary Angioedema Types I and II" was a major or minor topic of these publications.
![]()
To see the data from this visualization as text,
click here.
Below are the most recent publications written about "Hereditary Angioedema Types I and II" by people in Profiles over the past ten years.