TubeTalk Pronunciation
How to pronounce “severe combined immunodeficiency”
Hear “severe combined immunodeficiency” in real YouTube speech, then study definitions and example sentence snippets.
Pronunciation guide for severe combined immunodeficiency
- Learning goal
- Practice the English pronunciation of severe combined immunodeficiency with real speech in context.
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- Definition summary
- (pathology) A genetic disorder characterized by the disturbed development of functional T cells and B cells, resulting in extreme vulnerability to infectious diseases.
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A Deep Dive Into “severe combined immunodeficiency”
Meaning
- [Noun]
- (pathology) A genetic disorder characterized by the disturbed development of functional T cells and B cells, resulting in extreme vulnerability to infectious diseases.
Practice Nearby Words
mastocytosis, leukocyte adhesion deficiency, fanconi anemia, common variable immunodeficiency, sanfilippo syndrome, waardenburg syndrome, cold agglutinin disease, granulomatosis with polyangiitis, tuberous sclerosis, primary immunodeficiency, chédiak-higashi syndrome, wiskott-aldrich syndrome, hyperimmunoglobulin e syndrome, meckel-gruber syndrome, ataxia telangiectasia, dyskeratosis congenita, hemophagocytic lymphohistiocytosis, light chain deposition disease, canavan disease, lafora disease, alexander disease, opsoclonus myoclonus syndrome, familial dysautonomia, griscelli syndrome, felty's syndrome, camurati-engelmann disease, mixed connective tissue disease, gray platelet syndrome, pelizaeus-merzbacher disease, agranulocytosis, immunodeficiency, morquio syndrome, atypical hemolytic uremic syndrome, aceruloplasminemia, galactosemia, goodpasture syndrome, krabbe disease, mcleod syndrome, timothy syndrome, keutel syndrome, pyruvate dehydrogenase deficiency, aspartylglucosaminuria, chronic granulomatous disease, hunter syndrome, addison's disease, delta-beta thalassemia, faciodigitogenital dysplasia, sitosterolemia, aplastic anemia, gaucher's disease, evans syndrome, farber disease, haemophilia, cancer syndrome, systemic lupus erythematosus, erdheim-chester disease, leigh syndrome, primary ciliary dyskinesia, lennox-gastaut syndrome, methylmalonic acidemia, neurofibromatosis type ii, alkaptonuria, metachromatic leukodystrophy, bubble boy disease, cohen syndrome, 1p36 deletion syndrome, aicardi syndrome, alymphocytosis, essential thrombocythemia, crigler-najjar syndrome, histidinemia, feingold syndrome, urbach-wiethe disease, schnitzler syndrome, charge syndrome, stickler syndrome, myelodysplastic syndrome, agammaglobulinemia, caroli disease, bloom's syndrome, carpenter syndrome, menkes disease, eczema herpeticum, castleman disease, cowden syndrome, congenital myasthenic syndrome, lupus, lig4 syndrome, shwachman-diamond syndrome, wolf-hirschhorn syndrome, mast cell activation syndrome, type 1 diabetes, hypogammaglobulinemia, myotonic dystrophy, hereditary elliptocytosis, tyrosinemia type i, giant platelet disorder, robinow syndrome, schwannomatosis
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