MeSH Browser

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

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

X-Linked Combined Immunodeficiency Diseases MeSH Descriptor Data 2025