vrozený deficit komplementového systému [Hereditary Complement Deficiency Diseases]

tematický
5
Termíny

komplementové deficience
vrozené deficience komplementového systému
vrozené deficience komplementu
vrozené deficity komplementového systému
vrozený deficit složek komplementu

 

Complement Deficiencies
Inherited Complement Deficiency Diseases

Perzistentní odkaz   https://www.medvik.cz/link/D000081208
Definice

Genetické poruchy způsobené mutacemi genů pro proteiny komplementu. Jsou často klasifikované podle odlišné dráhy aktivace komplementu.

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 Prohlížeč
CUI
M000650095
Předchozí užití
Complement System Proteins (1971-2019); Immunologic Deficiency Syndromes (1971-2019)
Historická pozn.
2020
Veřejná pozn.
2020

C6 Deficiency, Subtotal Disease MeSH Prohlížeč

C9 Deficiency Disease MeSH Prohlížeč

C9 Deficiency with Dermatomyositis Disease MeSH Prohlížeč

Complement Component 3 Deficiency, Autosomal Recessive Disease MeSH Prohlížeč

Complement Component 4, Partial Deficiency Of Disease MeSH Prohlížeč

Complement Component 4a Deficiency Disease MeSH Prohlížeč

Complement Component 6 Deficiency Disease MeSH Prohlížeč

Complement Component 7 Deficiency Disease MeSH Prohlížeč

Complement Component C1s Deficiency Disease MeSH Prohlížeč

Complement Factor D Deficiency Disease MeSH Prohlížeč

Complement Factor H Deficiency Disease MeSH Prohlížeč

Complement Factor I Deficiency Disease MeSH Prohlížeč

Complement component 5 deficiency Disease MeSH Prohlížeč

MASP2 Deficiency Disease MeSH Prohlížeč

Properdin Deficiency, Type II Disease MeSH Prohlížeč

Properdin Deficiency, Type III Disease MeSH Prohlížeč

Properdin deficiency, X-linked Disease MeSH Prohlížeč