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Acquired agammaglobulinemia
Common variable agammaglobulinemia
Common variable hypogammaglobulinemia
Common variable immunodeficiency
Common variable unclassifiable immunodeficiency
Variable common cost
X-linked lymphoproliferative disease
X-linked lymphoproliferative syndrome

Translation of "Common variable immunodeficiency " (English → French) :

common variable immunodeficiency [ common variable unclassifiable immunodeficiency | acquired agammaglobulinemia | common variable agammaglobulinemia | common variable hypogammaglobulinemia ]

hypogammaglobulinémie à expression variable
Immunology
Immunologie


common variable immunodeficiency | common variable unclassifiable immunodeficiency | acquired agammaglobulinemia | common variable agammaglobulinemia | common variable hypogammaglobulinemia

hypogammaglobulinémie à expression variable
médecine > allergologie | biologie > immunologie
médecine > allergologie | biologie > immunologie


Common variable immunodeficiency

Déficit immunitaire commun variable
WORLD HEALTH ORGANIZATION ICD-10: D83
WORLD HEALTH ORGANIZATION ICD-10: D83


Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function

Déficit immunitaire commun variable avec anomalies prédominantes du nombre et de la fonction des lymphocytes B
WORLD HEALTH ORGANIZATION ICD-10: D83.0
WORLD HEALTH ORGANIZATION ICD-10: D83.0


Common variable immunodeficiency with predominant immunoregulatory T-cell disorders

Déficit immunitaire commun variable avec anomalies prédominantes des lymphocytes T immunorégulateurs
WORLD HEALTH ORGANIZATION ICD-10: D83.1
WORLD HEALTH ORGANIZATION ICD-10: D83.1


A rare genetic endocrine disease characterized by the association of common variable immunodeficiency manifesting with hypogammaglobulinemia and recurrent or severe childhood-onset sinopulmonary infections, followed, possibly many years later, by sym

syndrome d'insuffisance antéhypophysaire-déficit immunitaire variable
SNOMEDCT-BE (disorder) / 773664005
SNOMEDCT-BE (disorder) / 773664005


X-linked lymphoproliferative disease [ X-linked lymphoproliferative syndrome | X-linked immunodeficiency with undue susceptibility to Epstein-Barr virus | X-linked progressive combined variable immunodeficiency ]

syndrome lymphoprolifératif relié au chromosome X [ déficit immunitaire avec réponse anormale vis-à-vis du virus d'Epstein-Barr ]
Immunology
Immunologie


A rare form of diffuse large B-cell lymphoma occurring most commonly in patients over the age of 50 (usually between 70-75 years of age), without overt immunodeficiency, and presenting with nodal and extranodal involvement (in sites such as the stoma

lymphome B diffus à grandes cellules positif au virus Epstein-Barr chez les personnes âgées
SNOMEDCT-BE (usually between 70-75 years of age), without overt immunodeficiency, and presenting with nodal and extranodal involvement (in sites such as the stoma / 716788007
SNOMEDCT-BE (disorder) / 716788007


A rare benign nail tumor originating in the nail matrix characterized by localized pachyonychia and variable degrees of pigmentation: pigmented, melanocytic (common, longitudinal melanonychia that may simulate a foreign body) or hypopigmented. Histop

matricome onychocytique
SNOMEDCT-BE (common, longitudinal melanonychia that may simulate a foreign body) or hypopigmented. Histop / 773641008
SNOMEDCT-BE (disorder) / 773641008


variable common cost

coût commun variable
Accounting
Comptabilité




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'Common variable immunodeficiency'

Date index:2023-11-05 -

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