SCID


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SCIDSCID
  • noun

Synonyms for SCID

nouna congenital disease affecting T cells that can result from a mutation in any one of several different genes

Based on WordNet 3.0, Farlex clipart collection. © 2003-2012 Princeton University, Farlex Inc.
References in periodicals archive ?
A bone-marrow transplant from a genetically matched sibling can cure SCID, but most people lack a suitable donor.
In recipients from other donor types, which represent 86 per cent of cases, the data showed that the SCID genotype had a strong influence on survival and immune reconstitution.
So PHQ-9 positive/negative and SCID depression/non-depression can be summarized in the following 2x2 table with the R codes.
The genetic variant has previously been reported as disease-causing in a patient from a patient cohort with radiosensitive SCID and Omenn syndrome [12].
Although there was no chronic (>5 years) poliovirus excreter among the participants, we identified 1 patient with SCID as a long-term (>6 months) VDPV3 excreter who was excreting VDPV for 2 years.
The screening test for SCID and other causes of T cell lymphopenia is performed on dried blood spots, just as all other RUSP tests are.
A girl aged 6 months with severe combined immunodeficiency (SCID), who received OPV in March 2015, developed AFP in September 2015.
En estos estudios de calibracion clinica del CIDI, en comparacion con las entrevistas de reevaluacion clinica utilizando la Entrevista Diagnostica Estructurada SCID para el DSM-IV, reportan buena validez general.
A 1-year-old child known case of SCID (Diagnosed outside by peripheral blood cytometry] since 8 months of age presented to our hospital with septic shock.
Samuel Roberts was born with a severe combined immunodeficiency (SCID), which means his body cannot fight off infections.
GlobalData's clinical trial report, "Severe Combined Immune Deficiency (SCID) Global Clinical Trials Review, H2, 2015" provides an overview of Severe Combined Immune Deficiency (SCID) clinical trials scenario.
According to the FDA, newborns with severe combined immunodeficiency (SCID) typically have zero or low amounts of TREC DNA.
The most recent condition added to the US Recommended Uniform Screening Panel for newborn blood spot screening (NBS) is severe combined immunodeficiency (SCID) (9), a congenital disorder with severe impairment of cellular and humoral immune function due to a profound deficiency in T cells (10).