- Concept UI
- M0025206
- Scope Note
- 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.
- Terms
-
Mice, SCID
Preferred Term
Term UI
T049390
Date01/01/1999
LexicalTag
ACX
ThesaurusID
NLM (1992)
-
Immunodeficient Mice, Severe Combined
Term UI
T049386
Date10/24/1990
LexicalTag
NON
ThesaurusID
NLM (1992)
-
Severe Combined Immunodeficient Mice
Term UI
T049387
Date08/27/1990
LexicalTag
NON
ThesaurusID
NLM (1992)
-
Mouse, SCID
Term UI
T049388
Date08/27/1990
LexicalTag
NON
ThesaurusID
NLM (1992)
-
SCID Mice
Term UI
T049389
Date08/28/1990
LexicalTag
NON
ThesaurusID
NLM (1992)