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Descriptor English: Hereditary Complement Deficiency Diseases
Descriptor Spanish: Enfermedades por Deficiencia de Complemento Hereditario
Descriptor enfermedades de deficiencia hereditaria del complemento
Entry term(s) deficiencias del complemento
Scope note: Trastornos genéticos debidos a mutaciones en genes relacionados con PROTEÍNAS DEL SISTEMA DEL COMPLEMENTO. A menudo se clasifican según la vía específica en la que se encuentran localizadas las mutaciones causales (p. ej., vía clásica, vía de las lectinas, vía alternativa y vía terminal del complemento).
Descriptor Portuguese: Doenças da Deficiência Hereditária de Complemento
Descriptor French: Without translation
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 sang
CF liquide cérébrospinal
CI induit chimiquement
CL classification
CO complications
DG imagerie diagnostique
DH diétothérapie
DI diagnostic
DT traitement médicamenteux
EC économie
EH ethnologie
EM embryologie
EN enzymologie
EP épidémiologie
ET étiologie
GE génétique
HI histoire
IM immunologie
ME métabolisme
MI microbiologie
MO mortalité
NU soins infirmiers
PA anatomopathologie
PC prévention et contrôle
PP physiopathologie
PS parasitologie
PX psychologie
RH rééducation et réadaptation
RT radiothérapie
SU chirurgie
TH thérapie
UR urine
VE médecine vétérinaire
VI virologie
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



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