Hyper-IgM Immunodeficiency Syndrome, Type 1 [imunodeficience s hyper-IgM, typ 1]

topical
2
Terms

syndrom HIGM1
syndrom imunodeficience s hyper-IgM - typ 1
syndrom imunodeficience s hyper-IgM, typ 1
X-vázaná imunodeficience s hyper IgM

 

HIGM1
HIGM1 Syndrome
Hyper-IgM Immunodeficiency, X-Linked
Hyper-IgM Syndrome 1
Immunodeficiency with Hyper-IgM, Type 1
X-Linked Hyper IgM Syndrome

Persistent link   https://www.medvik.cz/link/D053307
Definition

An X-linked hyper-IgM immunodeficiency subtype resulting from mutation in the gene encoding CD40 LIGAND.

DUI
D053307 MeSH Browser
CUI
M0492429
Previous indexing
Immunologic Deficiency Syndromes (1995-2006); CD40 Ligand (2000-2006)
History note
2007
Public note
2007

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 1
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
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
C15.378 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
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.322 Genetic Diseases, X-Linked 59
C16.320.322.030 Aicardi Syndrome
C16.320.322.061 Androgen-Insensitivity Syndrome 56
C16.320.322.068 Barth Syndrome 6
C16.320.322.076 Bulbo-Spinal Atrophy, X-Linked 8
C16.320.322.092 Choroideremia 3
C16.320.322.100 Dent Disease 1
C16.320.322.108 Dyskeratosis Congenita 9
C16.320.322.116 Ectodermal Dysplasia 1, Anhidrotic 3
C16.320.322.124 Fabry Disease 187
C16.320.322.186 Focal Dermal Hypoplasia 6
C16.320.322.201 Glycogen Storage Disease Type IIb 11
C16.320.322.217 Glycogen Storage Disease Type VIII
C16.320.322.233 Granulomatous Disease, Chronic 54
C16.320.322.235 Hemophilia B 214
C16.320.322.237 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
C16.320.322.241 Ichthyosis, X-Linked 9
C16.320.322.370 Isolated Noncompaction of the Ventricular Myocardium 11
C16.320.322.500 X-Linked Intellectual Disability 17
C16.320.322.562 Muscular Dystrophy, Duchenne 133
C16.320.322.625 Muscular Dystrophy, Emery-Dreifuss 18
C16.320.322.750 Oculocerebrorenal Syndrome 9
C16.320.322.828 Ornithine Carbamoyltransferase Deficiency Disease 19
C16.320.322.906 Pelizaeus-Merzbacher Disease 11
C16.320.322.937 Wiskott-Aldrich Syndrome 20
C16.320.322.968 X-Linked Combined Immunodeficiency Diseases 4
C16.320.798 Primary Immunodeficiency Diseases 46
C16.320.798.625 Hyper-IgM Immunodeficiency Syndrome 4
C16.320.798.625.500 Hyper-IgM Immunodeficiency Syndrome, Type 1 2
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
C20.673.795 Primary Immunodeficiency Diseases 46
C20.673.795.625 Hyper-IgM Immunodeficiency Syndrome 4
C20.673.795.625.500 Hyper-IgM Immunodeficiency Syndrome, Type 1 2

Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic Disease MeSH Browser

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