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Descriptor English: Hereditary Complement Deficiency Diseases
Descriptor Spanish: Enfermedades por Deficiencia de Complemento Hereditario
Descriptor Portuguese: Doenças da Deficiência Hereditária de Complemento
Descriptor French: Without translation
Entry term(s): Complement Deficiencies
Complement Deficiency
Inherited Complement Deficiency Diseases
Tree number(s): C16.320.798.500
C20.673.795.500
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D000081208
Scope note: Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).
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: Complement System Proteins (1971-2019)
Immunologic Deficiency Syndromes (1971-2019)
Public MeSH Note: 2020
History Note: 2020
DeCS ID: 59119
Unique ID: D000081208
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2020/01/01
Date of Entry: 2019/07/08
Revision Date: 2019/06/17
Hereditary Complement Deficiency Diseases - Preferred
Concept UI M000650095
Scope note Genetic disorders due to mutations in genes involved in COMPLEMENT SYSTEM PROTEINS. They are often classified into distinct pathway of complement activation where causative mutations are found (e.g., classical pathway, lectin pathway, alternative pathway, and terminal complement pathway).
Preferred term Hereditary Complement Deficiency Diseases
Entry term(s) Inherited Complement Deficiency Diseases
Complement Deficiencies - Broader
Concept UI M000650120
Preferred term Complement Deficiencies
Entry term(s) Complement Deficiency



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