Hyper-IgM Immunodeficiency Syndrome [imunodeficience s hyper-IgM]

topical
4
Terms

hyper IgM syndrom
hyper-IgM syndrom
imunodeficience s hyper IgM
imunodeficience s hyper-IgM, typ 2
imunodeficience s hyper-IgM, typ 3
imunodeficience s hyper-IgM, typ 5
syndrom HIGM2
syndrom HIGM3
syndrom HIGM5
syndrom imunodeficience s hyper IgM, typ 3
syndrom imunodeficience s hyper-IgM
syndrom imunodeficience s hyper-IgM - typ 2
syndrom imunodeficience s hyper-IgM - typ 3
syndrom imunodeficience s hyper-IgM - typ 5
syndrom imunodeficience s hyper-IgM, typ 2
syndrom imunodeficience s hyper-IgM, typ 3
syndrom imunodeficience s hyper-IgM, typ 5

 

HIGM2 Syndrome
HIGM3 Syndrome
HIGM5 Syndrome
Hyper-IgM Immunodeficiency Syndrome Type 2
Hyper-IgM Immunodeficiency Syndrome Type 3
Hyper-IgM Immunodeficiency Syndrome Type 5
Hyper-IgM Immunodeficiency Syndrome, Type 2
Hyper-IgM Immunodeficiency Syndrome, Type 3
Hyper-IgM Immunodeficiency Syndrome, Type 5
Hyper-IgM Syndrome
Hyper-IgM Syndrome 2
Hyper-IgM Syndrome 3
Hyper-IgM Syndrome 5
Immunodeficiency with Hyper-IgM Syndrome
Immunodeficiency with Hyper-IgM, Type 2
Immunodeficiency with Hyper-IgM, Type 3
Immunodeficiency with Hyper-IgM, Type 5

Persistent link   https://www.medvik.cz/link/D053306
Definition

A rare inherited immunodeficiency syndrome characterized by normal or elevated serum IMMUNOGLOBULIN M levels with absence of IMMUNOGLOBULIN G; IMMUNOGLOBULIN A; and IMMUNOGLOBULIN E. It results in a profound susceptibility to BACTERIAL INFECTIONS and an increased susceptibility to OPPORTUNISTIC INFECTIONS. Several subtypes of hyper-IgM immunodeficiency syndrome exist depending upon the location of genetic mutation.

DUI
D053306 MeSH Browser
CUI
M0492421
Previous indexing
Immunoglobulin A (1995-2006); Immunoglobulin E (1995-2006); Immunoglobulin G (1995-2006); Immunoglobulin M (1995-2006); Immunologic Deficiency Syndromes (1995-2006)
History note
2007
Public note
2007

Allowable subheadings

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

C Diseases
C15 Hemic and Lymphatic Diseases 91
C15.378 Hematologic Diseases 975
C15.378.147 Blood Protein Disorders 126
C15.378.147.333 Dysgammaglobulinemia 10
C15.378.147.333.249 Hyper-IgM Immunodeficiency Syndrome 4
C15.378.147.333.249.500 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C15.378.147.333.500 IgA Deficiency 62
C15.378.147.333.750 IgG Deficiency 16
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
C16.320.798.250 Ataxia Telangiectasia 47
C16.320.798.313 Bloom Syndrome 11
C16.320.798.375 Chediak-Higashi Syndrome 4
C16.320.798.500 Hereditary Complement Deficiency Diseases 5
C16.320.798.625 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.798.625.500 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C16.320.798.688 Job Syndrome 15
C16.320.798.719 Leukocyte-Adhesion Deficiency Syndrome 3
C16.320.798.750 Severe Combined Immunodeficiency 63
C16.320.798.875 Wiskott-Aldrich Syndrome 20
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
C20.673 Immunologic Deficiency Syndromes 1 106
C20.673.430 Dysgammaglobulinemia 10
C20.673.430.250 Hyper-IgM Immunodeficiency Syndrome 4
C20.673.430.250.500 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C20.673.430.500 IgA Deficiency 62
C20.673.430.750 IgG Deficiency 16
C20.673.795 Primary Immunodeficiency Diseases 46
C20.673.795.250 Ataxia Telangiectasia 47
C20.673.795.313 Bloom Syndrome 11
C20.673.795.375 Chediak-Higashi Syndrome 4
C20.673.795.500 Hereditary Complement Deficiency Diseases 5
C20.673.795.625 Hyper-IgM Immunodeficiency Syndrome 4
C20.673.795.625.500 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C20.673.795.688 Job Syndrome 15
C20.673.795.719 Leukocyte-Adhesion Deficiency Syndrome 3
C20.673.795.750 Severe Combined Immunodeficiency 63
C20.673.795.875 Wiskott-Aldrich Syndrome 20

Immunodeficiency With Hyper-Igm, Type 4 Disease MeSH Browser

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