Hereditary Complement Deficiency Diseases [vrozený deficit komplementového systému]
topical
5
- Terms
-
komplementové deficience
vrozené deficience komplementového systému
vrozené deficience komplementu
vrozené deficity komplementového systému
vrozený deficit složek komplementu
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Complement Deficiencies
Inherited Complement Deficiency Diseases
Persistent link
https://www.medvik.cz/link/D000081208
Definition
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).
- DUI
- D000081208 MeSH Browser
- CUI
- M000650095
- Previous indexing
- Complement System Proteins (1971-2019); Immunologic Deficiency Syndromes (1971-2019)
- History note
- 2020
- Public note
- 2020
Allowable subheadings
- BL
- blood 0
- CF
- cerebrospinal fluid 0
- CI
- chemically induced 0
- CL
- classification 2
- CO
- complications 1
- DI
- diagnosis 4
- DG
- diagnostic imaging 0
- DH
- diet therapy 0
- DT
- drug therapy 1
- EC
- economics 0
- EM
- embryology 0
- EN
- enzymology 0
- EP
- epidemiology 0
- EH
- ethnology 0
- ET
- etiology 0
- GE
- genetics 1
- HI
- history 0
- IM
- immunology 1
- ME
- metabolism 0
- MI
- microbiology 0
- MO
- mortality 0
- NU
- nursing 0
- PS
- parasitology 0
- PA
- pathology 0
- PP
- physiopathology 2
- PC
- prevention & control 0
- PX
- psychology 0
- RT
- radiotherapy 0
- RH
- rehabilitation 0
- SU
- surgery 0
- TH
- therapy 3
- UR
- urine 0
- VE
- veterinary 0
- VI
- virology 0
...
Occurrences in Medvik records
C
Diseases