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bn:00069669n
Noun Concept
SYL
No term available
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
Relations
Sources
IS A
EN
immunodeficiency
EN
monogenic disorder
EN
lymphocytopenia
EN
combined immunodeficiencies
HAS KIND
EN
ADA-SCID
EN
X-linked SCID
EN
Omenn syndrome
EN
janus kinase-3 deficiency
EN
Reticular dysgenesis
+3 relations
HEALTH SPECIALTY
EN
immunology
SAID TO BE THE SAME AS
EN
severe combined immunodeficiency

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