Hereditary Angioedema Types I and II

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.

Year introduced: 2010

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Tree Number(s): C14.907.079.500.750, C17.800.862.945.066.500.750, C20.543.480.904.066.500.750

MeSH Unique ID: D056829

Entry Terms:

• C1 Esterase Inhibitor, Deficiency Of
• Deficiency of C1 Esterase Inhibitor
• Hereditary Angioedema Type 1
• Angioedema, Hereditary, Types I and II
• Hereditary Angioedema Type I
• Angioedema, Hereditary, Type I
• Hereditary Angioedema Type II
• Angioedema, Hereditary, Type II

Previous Indexing:

• Angioedema (1964-2007)
• Angioedemas, Hereditary (2007-2009)

See Also:

• Complement C1 Inhibitor Protein

All MeSH Categories
Diseases Category
Cardiovascular Diseases
Vascular Diseases
Angioedema
Angioedemas, Hereditary
Hereditary Angioedema Types I and II

All MeSH Categories
Diseases Category
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Vascular
Urticaria
Angioedema
Angioedemas, Hereditary
Hereditary Angioedema Types I and II

All MeSH Categories
Diseases Category
Immune System Diseases
Hypersensitivity
Hypersensitivity, Immediate
Urticaria
Angioedema
Angioedemas, Hereditary
Hereditary Angioedema Types I and II