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

 

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
CF
cerebrospinal fluid
CI
chemically induced
CL
classification 2
CO
complications 1
DI
diagnosis 4
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy 1
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology
GE
genetics 1
HI
history
IM
immunology 1
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology 2
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 3
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 215
C16.320.798 Primary Immunodeficiency Diseases 48
C16.320.798.250 Ataxia Telangiectasia 48
C16.320.798.313 Bloom Syndrome 11
C16.320.798.375 Chediak-Higashi Syndrome 4
C16.320.798.500 Hereditary Complement Deficiency Diseases 5
C16.320.798.500.500 Angioedemas, Hereditary 86
C16.320.798.625 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.798.688 Job Syndrome 16
C16.320.798.719 Leukocyte-Adhesion Deficiency Syndrome 3
C16.320.798.750 Severe Combined Immunodeficiency 64
C16.320.798.875 Wiskott-Aldrich Syndrome 20
C20 Immune System Diseases 748
C20.673 Immunologic Deficiency Syndromes 1 110
C20.673.795 Primary Immunodeficiency Diseases 48
C20.673.795.250 Ataxia Telangiectasia 48
C20.673.795.313 Bloom Syndrome 11
C20.673.795.375 Chediak-Higashi Syndrome 4
C20.673.795.500 Hereditary Complement Deficiency Diseases 5
C20.673.795.500.500 Angioedemas, Hereditary 86
C20.673.795.625 Hyper-IgM Immunodeficiency Syndrome 4
C20.673.795.688 Job Syndrome 16
C20.673.795.719 Leukocyte-Adhesion Deficiency Syndrome 3
C20.673.795.750 Severe Combined Immunodeficiency 64
C20.673.795.875 Wiskott-Aldrich Syndrome 20

C6 Deficiency, Subtotal Disease MeSH Browser

C9 Deficiency Disease MeSH Browser

C9 Deficiency with Dermatomyositis Disease MeSH Browser

Complement Component 3 Deficiency, Autosomal Recessive Disease MeSH Browser

Complement Component 4, Partial Deficiency Of Disease MeSH Browser

Complement Component 4a Deficiency Disease MeSH Browser

Complement Component 6 Deficiency Disease MeSH Browser

Complement Component 7 Deficiency Disease MeSH Browser

Complement Component C1s Deficiency Disease MeSH Browser

Complement Factor D Deficiency Disease MeSH Browser

Complement Factor H Deficiency Disease MeSH Browser

Complement Factor I Deficiency Disease MeSH Browser

Complement component 5 deficiency Disease MeSH Browser

MASP2 Deficiency Disease MeSH Browser

Properdin Deficiency, Type II Disease MeSH Browser

Properdin Deficiency, Type III Disease MeSH Browser

Properdin deficiency, X-linked Disease MeSH Browser

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