Severe Combined Immunodeficiency
Of monogenic disorder and immunodeficiency. May also be referred to as SCID and severe combined immunodeficiency disease.
A congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of life.
This concept's ID is @1~71167
Contains
- X-linked SCID
SCID in male children resulting from mutation of a gene that codes for a protein on...
- ADA-SCID
SCID resulting from mutation of a gene that codes for adenosine deaminase.