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

tematický
4
Termíny

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

Perzistentní odkaz   https://www.medvik.cz/link/D053632
Definice

Formy kombinované imunodeficience způsobené mutacemi genu pro společnou gama-podjednotku interleukinových receptorů. Byly identifikované podtypy onemocnění s různě závažnými klinickými projevy.

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 Prohlížeč
CUI
M0495084
Předchozí užití
Severe Combined Immunodeficiency (1991-2006)
Historická pozn.
2007
Veřejná pozn.
2007

C Nemoci
C16.320.322.030 Aicardiho syndrom
C16.320.322.068 Barthův syndrom 6
C16.320.322.092 choroideremie 3
C16.320.322.100 Dentova choroba 1
C16.320.322.108 dyskeratosis congenita 9
C16.320.322.124 Fabryho nemoc 187
C16.320.322.201 glykogenóza typu IIb 11
C16.320.322.217 glykogenóza typu VIII
C16.320.322.235 hemofilie B 214
C16.614 nemoci novorozenců 1 946