bn:00069669n
Noun Concept
Categories: Rare diseases, Genetic disorders by system, Combined T and B–cell immunodeficiencies, Noninfectious immunodeficiency-related cutaneous conditions, DNA replication and repair-deficiency disorders
EN
severe combined immunodeficiency  severe combined immunodeficiency disease  SCID  alymphocytosis  Ashanthi De Silva
EN
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 WordNet 3.0
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EN
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 WordNet 3.0 & Open English WordNet
Severe combined immunodeficiency, also known as Swiss-type agammaglobulinemia, is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in differing clinical presentations. Wikipedia
Combined T cell and B cell immunodeficiency that is caused by a defect in several genes encoding for B and T lymphocytes resulting in individuals with non-functional immune systems Wikidata
A genetic disorder in which lymphocyte proliferation is inhibited and the immune system is compromised. Wiktionary
Genetic disorder in which lymphocyte proliferation is inhibited. Wiktionary (translation)