| 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: | Déficits héréditaires en complément | ||||||
| Entry term(s): |
Complement Deficiencies Complement Deficiency Inherited Complement Deficiency Diseases |
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| 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 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 |
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| Previous Indexing: |
Complement System Proteins (1971-2019) Immunologic Deficiency Syndromes (1971-2019) |
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| Public MeSH Note: | 2020 |
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| History Note: | 2020 |
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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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Hereditary Complement Deficiency Diseases
- Preferred
Complement Deficiencies
- Broader
| 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 |
| Concept UI |
M000650120 |
| Preferred term | Complement Deficiencies |
| Entry term(s) |
Complement Deficiency |
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