Structured Summary
Abstract
Mice homozygous for the mutant autosomal recessive gene scid which is located on the centromeric end of chromosome 16. These mice lack mature, functional lymphocytes and are thus highly susceptible to lethal opportunistic infections if not chronically treated with antibiotics. The lack of B- and T-cell immunity resembles severe combined immunodeficiency (SCID) syndrome in human infants. SCID mice are useful as animal models since they are receptive to implantation of a human immune system producing SCID-human (SCID-hu) hematochimeric mice.
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Classification
Broader headings
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Synonyms
11 entry terms
- Immunodeficient Mice, Severe Combined
- Mice, SCID
- Mouse, SCID
- Severe Combined Immunodeficient Mice
- SCID Mouse
- Mouse, SCID-hu
- SCID-hu Mice
- Mice, SCID-hu
- Mouse, SCID hu
- SCID hu Mice
- SCID-hu Mouse
MeSH Record
Aspects Covered
18 allowable subheadings
Indexed with the subheadings abnormalities, anatomy & histology, blood, cerebrospinal fluid, classification, embryology, genetics, growth & development, immunology, injuries, metabolism, microbiology, parasitology, physiology, psychology, surgery, urine, virology.
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Indexing Annotation
NIM with no qualifiers when experimental animal
MeSH Record
History Note
92
MeSH Record
Previous Indexing
- Mice, Mutant Strains (1983-1991)
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AMA Style
References
- National Library of Medicine. SCID Mice. Medical Subject Headings (MeSH). 2026. Unique ID D016513. http://id.nlm.nih.gov/mesh/2026/D016513
- SCID Mice. In: Wikipedia. https://en.wikipedia.org/wiki/Severe_combined_immunodeficient_mice
- SCID Mice. In: Wikidata. https://www.wikidata.org/wiki/Q30324043