Structured Summary
Abstract
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.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
See Also
MeSH Record
Synonyms
8 entry terms
- Angioedema, Hereditary, Types I and II
- C1 Esterase Inhibitor, Deficiency Of
- Deficiency of C1 Esterase Inhibitor
- Hereditary Angioedema Type 1
- Angioedema, Hereditary, Type I
- Angioedema, Hereditary, Type II
- Hereditary Angioedema Type I
- Hereditary Angioedema Type II
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2010
MeSH Record
Previous Indexing
- Angioedema (1964-2007)
- Angioedemas, Hereditary (2007-2009)
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Hereditary Angioedema Types I and II. Medical Subject Headings (MeSH). 2026. Unique ID D056829. http://id.nlm.nih.gov/mesh/2026/D056829
- Hereditary Angioedema Types I and II. In: Wikidata. https://www.wikidata.org/wiki/Q55082403