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Descriptor English: Hereditary Angioedema Types I and II
Descriptor Spanish: Angioedema Hereditario Tipos I y II
Descriptor angioedema hereditario de los tipos I y II
Scope note: Formas de angioedema hereditario que se producen debido a mutaciones en el gen de la PROTEÍNA INHIBIDORA DEL COMPLEMENTO C1. El angioedema hereditario tipo I se asocia con concentraciones séricas reducidas de proteína inhibidora del complemento C1. El angioedema hereditario de tipo II se asocia con la producción de una proteína inhibidora del complemento C1 disfuncional. 
Descriptor Portuguese: Angioedema Hereditário Tipos I e II
Descriptor French: Angioedèmes héréditaires de types I et II
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
Tree number(s): C14.907.079.500.750
C17.800.862.945.066.500.750
C20.543.480.904.066.500.750
RDF Unique Identifier: https://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.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Angioedema (1964-2007)
Angioedemas, Hereditary (2007-2009)
Public MeSH Note: 2010
History Note: 2010
Related: Complement C1 Inhibitor Protein MeSH
DeCS ID: 53541
Unique ID: D056829
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2010/01/01
Date of Entry: 2009/07/06
Revision Date: 2012/07/03
Hereditary Angioedema Types I and II - Preferred
Concept UI M0529318
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.
Preferred term Hereditary Angioedema Types I and II
Entry term(s) Angioedema, Hereditary, Types I and II
C1 Esterase Inhibitor, Deficiency Of
Deficiency of C1 Esterase Inhibitor
Hereditary Angioedema Type 1
Hereditary Angioedema Type I - Narrower
Concept UI M0529319
Preferred term Hereditary Angioedema Type I
Entry term(s) Angioedema, Hereditary, Type I
Hereditary Angioedema Type II - Narrower
Concept UI M0529320
Preferred term Hereditary Angioedema Type II
Entry term(s) Angioedema, Hereditary, Type II



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