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X-Linked Combined Immunodeficiency Diseases MeSH Descriptor Data 2021


MeSH Heading
X-Linked Combined Immunodeficiency Diseases
Tree Number(s)
C16.320.322.968
C16.320.798.750.500
C16.614.815.500
C20.673.795.750.500
Unique ID
D053632
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D053632
Scope Note
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.
Entry Term(s)
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
NLM Classification #
QW 740
Previous Indexing
Severe Combined Immunodeficiency (1991-2006)
Public MeSH Note
2007
History Note
2007
Date Established
2007/01/01
Date of Entry
2006/07/05
Revision Date
2019/06/17
X-Linked Combined Immunodeficiency Diseases Preferred
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