Autoimmune Lymphoproliferative Syndrome [autoimunitní lymfoproliferativní syndrom]

topical
2
Terms

ALPS
ALPS asociovaný s mutací kaspáz 8
autoimunitní lymfoproliferativní syndrom typ 1 - autozomálně dominantní
autoimunitní lymfoproliferativní syndrom typ 2B
autoimunitní lymfoproliferativní syndrom typu 1, autozomálně dominantní
autoimunitní lymfoproliferativní syndrom typu 2B
Canalové-Smithův syndrom
deficience kaspázy 8
deficit kaspázy 8
kaspasa 8 - deficience
kaspáza 8 - deficit
syndrom Canalové-Smithův

 

Autoimmune Lymphoproliferative Syndrome Type 1, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B (ALPS2B)
Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Dominant
Autoimmune Lymphoproliferative Syndrome, Type IIb
Canale Smith Syndrome
Canale-Smith Syndrome
Caspase 8 Deficiency
Caspase-8 Deficiency

Persistent link   https://www.medvik.cz/link/D056735
Definition

Rare congenital lymphoid disorder due to mutations in certain Fas-Fas ligand pathway genes. Known causes include mutations in FAS, TNFSF6, NRAS, CASP8, and CASP10 proteins. Clinical features include LYMPHADENOPATHY; SPLENOMEGALY; and AUTOIMMUNITY.

DUI
D056735 MeSH Browser
CUI
M0528916
Previous indexing
Autoimmune Diseases (1997-2009); Lymphoproliferative Disorders (1983-2009)
History note
2010
Public note
2010

Allowable subheadings

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

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.604 Lymphatic Diseases 444
C15.604.515 Lymphoproliferative Disorders 182
C15.604.515.032 Agammaglobulinemia 113
C15.604.515.138 Autoimmune Lymphoproliferative Syndrome 2
C15.604.515.245 Castleman Disease 61
C15.604.515.292 Granuloma 236
C15.604.515.435 Heavy Chain Disease 8
C15.604.515.509 Immunoblastic Lymphadenopathy 10
C15.604.515.516 Infectious Mononucleosis 191
C15.604.515.553 Leukemia, Hairy Cell 95
C15.604.515.560 Leukemia, Lymphoid 477
C15.604.515.562 Lymphangiomyoma 1
C15.604.515.569 Lymphoma 1 119
C15.604.515.700 Marek Disease 7
C15.604.515.827 Sarcoidosis 500
C15.604.515.841 Sezary Syndrome 43
C15.604.515.880 Tumor Lysis Syndrome 38
C15.604.515.925 Waldenstrom Macroglobulinemia 112
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.033 Adrenal Hyperplasia, Congenital 225
C16.320.051 Alagille Syndrome 19
C16.320.060 alpha 1-Antitrypsin Deficiency 83
C16.320.070 Anemia, Hemolytic, Congenital 48
C16.320.077 Anemia, Hypoplastic, Congenital 3
C16.320.080 Ataxia Telangiectasia 47
C16.320.089 Autoimmune Lymphoproliferative Syndrome 2
C16.320.099 Blood Coagulation Disorders, Inherited 61
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.144 Camurati-Engelmann Syndrome 6
C16.320.160 Cardiomyopathy, Hypertrophic, Familial 32
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 259
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 328
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 97
C16.320.290 Eye Diseases, Hereditary 57
C16.320.298 Familial Multiple Lipomatosis
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 1
C16.320.322 Genetic Diseases, X-Linked 59
C16.320.338 Genetic Diseases, Y-Linked 1
C16.320.355 Hajdu-Cheney Syndrome 6
C16.320.365 Hemoglobinopathies 68
C16.320.382 Hereditary Autoinflammatory Diseases 46
C16.320.400 Heredodegenerative Disorders, Nervous System 45
C16.320.413 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.427 Hyperthyroxinemia, Familial Dysalbuminemic 1
C16.320.447 Imprinting Disorders
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.495 Lennox Gastaut Syndrome 5
C16.320.510 Loeys-Dietz Syndrome 7
C16.320.540 Marfan Syndrome 105
C16.320.565 Metabolism, Inborn Errors 711
C16.320.577 Muscular Dystrophies 140
C16.320.590 Myasthenic Syndromes, Congenital 20
C16.320.600 Nail-Patella Syndrome 8
C16.320.700 Neoplastic Syndromes, Hereditary 143
C16.320.709 Oculocerebrorenal Syndrome 9
C16.320.714 Orofaciodigital Syndromes 7
C16.320.718 Osteoarthropathy, Primary Hypertrophic 127
C16.320.728 Osteochondrodysplasias 123
C16.320.737 Osteogenesis Imperfecta 106
C16.320.775 Pain Insensitivity, Congenital 10
C16.320.784 Pelger-Huet Anomaly 7
C16.320.798 Primary Immunodeficiency Diseases 46
C16.320.812 Pycnodysostosis 2
C16.320.831 Renal Tubular Transport, Inborn Errors 36
C16.320.850 Skin Diseases, Genetic 89
C16.320.925 Werner Syndrome 14
C16.320.962 Yellow Nail Syndrome
C20 Immune System Diseases 746
C20.111 Autoimmune Diseases 1 934
C20.111.163 Addison Disease 128
C20.111.175 Anemia, Hemolytic, Autoimmune 89
C20.111.190 Anti-Glomerular Basement Membrane Disease 47
C20.111.193 Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis 119
C20.111.197 Antiphospholipid Syndrome 281
C20.111.198 Arthritis, Juvenile 474
C20.111.199 Arthritis, Rheumatoid 3 116
C20.111.258 Autoimmune Diseases of the Nervous System 94
C20.111.273 Autoimmune Hypophysitis 7
C20.111.288 Autoimmune Lymphoproliferative Syndrome 2
C20.111.296 Autoimmune Pancreatitis 16
C20.111.303 Birdshot Chorioretinopathy
C20.111.318 Dermatitis Herpetiformis 87
C20.111.327 Diabetes Mellitus, Type 1 3 002
C20.111.525 Glomerulonephritis, IGA 210
C20.111.535 Glomerulonephritis, Membranous 79
C20.111.555 Graves Disease 255
C20.111.567 Hepatitis, Autoimmune 83
C20.111.572 Immunoglobulin G4-Related Disease 26
C20.111.576 Latent Autoimmune Diabetes in Adults 15
C20.111.585 Linear IgA Bullous Dermatosis 15
C20.111.590 Lupus Erythematosus, Systemic 1 091
C20.111.709 Ophthalmia, Sympathetic 17
C20.111.730 Pemphigoid, Bullous 87
C20.111.736 Pemphigus 208
C20.111.750 Polyendocrinopathies, Autoimmune 110
C20.111.759 Purpura, Thrombocytopenic, Idiopathic 171
C20.111.809 Thyroiditis, Autoimmune 365
C20.111.904 Undifferentiated Connective Tissue Diseases 3
C20.683 Immunoproliferative Disorders 19
C20.683.515 Lymphoproliferative Disorders 182
C20.683.515.124 Autoimmune Lymphoproliferative Syndrome 2
C20.683.515.250 Castleman Disease 61
C20.683.515.501 Immunoblastic Lymphadenopathy 10
C20.683.515.507 Immunoglobulin Light-chain Amyloidosis 37
C20.683.515.512 Immunoproliferative Small Intestinal Disease 3
C20.683.515.515 Infectious Mononucleosis 191
C20.683.515.517 Leukemia, Hairy Cell 95
C20.683.515.528 Leukemia, Lymphoid 477
C20.683.515.710 Lymphangiomyoma 1
C20.683.515.761 Lymphoma 1 119
C20.683.515.800 Macrophage Activation Syndrome 7
C20.683.515.840 Marek Disease 7
C20.683.515.845 Multiple Myeloma 1 782
C20.683.515.880 Plasmacytoma 179
C20.683.515.920 Sezary Syndrome 43
C20.683.515.950 Tumor Lysis Syndrome 38

Autoimmune Lymphoproliferative Syndrome, Type I, Autosomal Recessive Disease MeSH Browser

Autoimmune Lymphoproliferative Syndrome, Type IA Disease MeSH Browser

Autoimmune Lymphoproliferative Syndrome, Type IB Disease MeSH Browser

Autoimmune Lymphoproliferative Syndrome, Type IIA Disease MeSH Browser

Dianzani autoimmune lymphoproliferative syndrome Disease MeSH Browser

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