Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Infant, Newborn, Diseases
Severe Combined Immunodeficiency
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Severe Combined Immunodeficiency
Preferred term
X-Linked Combined Immunodeficiency Diseases
Type
-
Topical Descriptor
Broader concept
Entry terms
- Combined Immunodeficiency, X Linked
- Combined Immunodeficiency, X-Linked
- Immunodeficiency 4
- Immunodeficiency 6
- Immunodeficiency Diseases, X-Linked
- Immunodeficiency Diseases, X Linked Combined
- Immunodeficiency Diseases, X-Linked Combined
- Immunodeficiency Disease, X-Linked
- Immunodeficiency Syndromes, X-Linked
- Immunodeficiency Syndrome, X-Linked
- Immunodeficiency, X-Linked Combined
- SCIDs, X-Linked
- SCIDX
- SCIDX1
- SCID, X Linked
- SCID, X-Linked
- Severe Combined Immunodeficiency, X Linked
- 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 Immunodeficiencies
- X Linked Combined Immunodeficiency
- X-Linked Combined Immunodeficiency
- X Linked Immunodeficiency Disease
- X-Linked Immunodeficiency Disease
- X-Linked Immunodeficiency Diseases
- X Linked Immunodeficiency Syndrome
- X-Linked Immunodeficiency Syndrome
- X-Linked Immunodeficiency Syndromes
- X Linked SCID
- X-Linked SCID
- X-Linked SCIDs
- X Linked Severe Combined Immunodeficiency
- X-Linked Severe Combined Immunodeficiency
- X-SCID
- XSCID
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.
History note
- 2007
In other languages
-
Finnish
-
X-kromosomaalinen kombinoitunut immuunivajaussairaus
-
Immunbrist 4
Swedish
URI
http://www.yso.fi/onto/mesh/D053632
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