X-Linked Combined Immunodeficiency Diseases [kombinované imunodeficience vázané na chromozom X]

topical
4
Terms

imunodeficience 4
imunodeficience 6
imunodeficience vázaná na chromozóm X
kombinované imunodeficience vázané na chromozóm X
SCIDX
SCIDX1
těžké kombinované imunodeficience vázané na chromozóm X
X-SCID
XSCID

 

Combined Immunodeficiency, X-Linked
Immunodeficiency 4
Immunodeficiency 6
Immunodeficiency Diseases, X-Linked Combined
SCID, X-Linked
SCIDX
SCIDX1
Severe Combined Immunodeficiency, X-Linked
Severe Combined Immunodeficiency, X-Linked, T Cell Negative, B Cell Positive, NK Cell Negative
Severe Combined Immunodeficiency, X-Linked, T Cell-Negative, B Cell-Positive, NK Cell-Negative
X-Linked Combined Immunodeficiency
X-Linked Immunodeficiency Disease
X-Linked Immunodeficiency Syndrome
X-Linked SCID
X-Linked Severe Combined Immunodeficiency
X-SCID
XSCID

Persistent link   https://www.medvik.cz/link/D053632
Definition

Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.

DUI
D053632 MeSH Browser
CUI
M0495084
Previous indexing
Severe Combined Immunodeficiency (1991-2006)
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 1
NU
nursing
PS
parasitology
PA
pathology
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 3
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 219
C16.320.322 Genetic Diseases, X-Linked 61
C16.320.322.030 Aicardi Syndrome
C16.320.322.061 Androgen-Insensitivity Syndrome 57
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 192
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 221
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 18
C16.320.322.562 Muscular Dystrophy, Duchenne 136
C16.320.322.625 Muscular Dystrophy, Emery-Dreifuss 18
C16.320.322.750 Oculocerebrorenal Syndrome 9
C16.320.322.828 Ornithine Carbamoyltransferase Deficiency Disease 20
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 51
C16.320.798.750 Severe Combined Immunodeficiency 65
C16.320.798.750.500 X-Linked Combined Immunodeficiency Diseases 4
C16.614 Infant, Newborn, Diseases 1 952
C16.614.815 Severe Combined Immunodeficiency 65
C16.614.815.500 X-Linked Combined Immunodeficiency Diseases 4
C20 Immune System Diseases 749
C20.673 Immunologic Deficiency Syndromes 1 112
C20.673.795 Primary Immunodeficiency Diseases 51
C20.673.795.750 Severe Combined Immunodeficiency 65
C20.673.795.750.500 X-Linked Combined Immunodeficiency Diseases 4

Woods Black Norbury syndrome Disease MeSH Browser

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