primární imunodeficience [Primary Immunodeficiency Diseases]
- Termíny
-
kongenitální imunodeficience
kongenitální imunodeficitní stavy
kongenitální imunodeficity
primární imunitní deficity
primární imunodeficitní onemocnění
primární imunodeficitní stavy
primární imunodeficitní syndromy
primární imunodeficity
primární poruchy imunitního systému
primární protilátkové deficience
primární protilátkové deficity
primární protilátkové imunodeficience
primární protilátkové imunodeficity
vrozené imunodeficience
vrozené imunodeficitní stavy
vrozené imunodeficity
-
Congenital Immunodeficiency Disease
Congenital Immunodeficiency Diseases
Congenital Immunodeficiency Disorder
Congenital Immunodeficiency Disorders
Congenital Immunodeficiency Syndrome
Congenital Immunodeficiency Syndromes
Inherited Immunodeficiency Disease
Inherited Immunodeficiency Diseases
Inherited Immunodeficiency Disorder
Inherited Immunodeficiency Disorders
Inherited Immunodeficiency Syndrome
Inherited Immunodeficiency Syndromes
Primary Antibody Deficiencies
Primary Antibody Deficiency Disorder
Primary Antibody Deficiency Disorders
Primary Antibody Deficiency Syndrome
Primary Antibody Deficiency Syndromes
Primary Immune Deficiency
Primary Immune Deficiency Disease
Primary Immune Deficiency Diseases
Primary Immune Deficiency Disorder
Primary Immune Deficiency Disorders
Primary Immune Deficiency Syndrome
Primary Immune Deficiency Syndromes
Primary Immunodeficiency Disease
Primary Immunodeficiency Disorder
Primary Immunodeficiency Disorders
Primary Immunodeficiency Syndromes
Geneticky podmíněné nemoci a syndromy vyvolané mutacemi genů, které se podílejí na funkci imunitního systému. To se projevuje zvýšenou náchylností k infekčním onemocněním, často v souvislosti s autoimunitními manifestacemi.
Genetic immunologic deficiency diseases and syndromes due to mutations in genes involved in IMMUNITY generally characterized by an increased susceptibility to infectious diseases. They are often associated with AUTOIMMUNE DISEASE manifestations.
- DUI
- D000081207 MeSH Prohlížeč
- CUI
- M000650094
- Předchozí užití
- Immunologic Deficiency Syndromes (1972-2019)
- Historická pozn.
- 2020
- Veřejná pozn.
- 2020
Povolená podhesla
- CI
- chemicky indukované
- SU
- chirurgie
- HI
- dějiny
- DG
- diagnostické zobrazování
- DI
- diagnóza 21
- DH
- dietoterapie
- EC
- ekonomika
- EM
- embryologie
- EN
- enzymologie
- EP
- epidemiologie 3
- ET
- etiologie 1
- EH
- etnologie
- DT
- farmakoterapie 4
- GE
- genetika 12
- IM
- imunologie 6
- CL
- klasifikace 7
- CO
- komplikace 5
- BL
- krev
- ME
- metabolismus
- MI
- mikrobiologie 1
- UR
- moč
- MO
- mortalita
- CF
- mozkomíšní mok
- NU
- ošetřování
- PS
- parazitologie
- PP
- patofyziologie 2
- PA
- patologie 3
- PC
- prevence a kontrola
- PX
- psychologie
- RT
- radioterapie
- RH
- rehabilitace
- TH
- terapie 15
- VE
- veterinární
- VI
- virologie
Activated PI3K-delta Syndrome Disease MeSH Prohlížeč
Antibody Deficiency due to Defect in CD19 Disease MeSH Prohlížeč
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations Disease MeSH Prohlížeč
CD8 Deficiency, Familial Disease MeSH Prohlížeč
Cartilage hair hypoplasia like syndrome Disease MeSH Prohlížeč
Cartilage-hair hypoplasia Disease MeSH Prohlížeč
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant Disease MeSH Prohlížeč
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Disease MeSH Prohlížeč
Ectodermal dysplasia, hypohidrotic, with immune deficiency Disease MeSH Prohlížeč
Enteropathy, Familial, with Villous Edema and Immunoglobulin G2 Deficiency Disease MeSH Prohlížeč
Griscelli syndrome type 2 Disease MeSH Prohlížeč
IRAK4 Deficiency Disease MeSH Prohlížeč
Immune Deficiency, Familial Variable Disease MeSH Prohlížeč
Immunodeficiency due to Defect in CD3-Zeta Disease MeSH Prohlížeč
Immunodeficiency syndrome, variable Disease MeSH Prohlížeč
Immunodeficiency, Hypogammaglobulinemia, and Reduced B Cells Disease MeSH Prohlížeč
Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein Disease MeSH Prohlížeč
Kotzot-Richter syndrome Disease MeSH Prohlížeč
MYD88 Deficiency Disease MeSH Prohlížeč
NEMO mutation with immunodeficiency Disease MeSH Prohlížeč
Neutrophil Immunodeficiency Syndrome Disease MeSH Prohlížeč
Purine Nucleoside Phosphorylase Deficiency Disease MeSH Prohlížeč
Riddle Syndrome Disease MeSH Prohlížeč
Roifman syndrome Disease MeSH Prohlížeč
Roifman-Chitayat Syndrome Disease MeSH Prohlížeč
Schimke immunoosseous dysplasia Disease MeSH Prohlížeč
Splenic Hypoplasia Disease MeSH Prohlížeč
T cell immunodeficiency primary Disease MeSH Prohlížeč
Thumb Agenesis, Short Stature, And Immunodeficiency Disease MeSH Prohlížeč
Tuftsin Deficiency Disease MeSH Prohlížeč
WHIM syndrome Disease MeSH Prohlížeč