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Hereditary Angioedema Types I and II MeSH Descriptor Data 2022


MeSH Heading
Hereditary Angioedema Types I and II
Tree Number(s)
C14.907.079.500.750
C17.800.862.945.066.500.750
C20.543.480.904.066.500.750
Unique ID
D056829
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D056829
Scope Note
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.
Entry Term(s)
Angioedema, Hereditary, Type I
Angioedema, Hereditary, Type II
Angioedema, Hereditary, Types I and II
C1 Esterase Inhibitor, Deficiency Of
Deficiency of C1 Esterase Inhibitor
Hereditary Angioedema Type 1
Hereditary Angioedema Type I
Hereditary Angioedema Type II
Previous Indexing
Angioedema (1964-2007)
Angioedemas, Hereditary (2007-2009)
See Also
Complement C1 Inhibitor Protein
Public MeSH Note
2010
History Note
2010
Date Established
2010/01/01
Date of Entry
2009/07/06
Revision Date
2012/07/03
Hereditary Angioedema Types I and II Preferred
Hereditary Angioedema Type I Narrower
Hereditary Angioedema Type II Narrower
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