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Descriptor English: | Hereditary Complement Deficiency Diseases | ||||||
Descriptor Spanish: |
Enfermedades por Deficiencia de Complemento Hereditario
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Descriptor Portuguese: | Doenças da Deficiência Hereditária de Complemento | ||||||
Descriptor French: | Without translation | ||||||
Tree number(s): |
C16.320.798.500 C20.673.795.500 |
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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). |
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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 |
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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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