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Acquired agammaglobulinemia
CVAgamma
Common variable agammaglobulinemia
Common variable hypogammaglobulinemia
Common variable immunodeficiency
Common variable unclassifiable immunodeficiency
Hypogammaglobulinaemia NOS
Variable common cost
Variable common current cost

Translation of "common variable agammaglobulinemia " (English → French) :

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

hypogammaglobulinémie à expression variable


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

hypogammaglobulinémie à expression variable


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


Common variable immunodeficiency

Déficit immunitaire commun variable


Agammaglobulinaemia with immunoglobulin-bearing B-lymphocytes Common variable agammaglobulinaemia [CVAgamma] Hypogammaglobulinaemia NOS

Agammaglobulinémie:avec lymphocytes B porteurs d'immunoglobulines | commune variable | Hypogammaglobulinémie SAI


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


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


A newly described syndrome associated with a variable clinical phenotype including developmental delay, facial dysmorphism, short neck and diverse malformations. Eight cases have been reported to date. The most common facial features include eye anom

syndrome de microdélétion 6p22




variable common current cost

coût commun variable actualisé




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'common variable agammaglobulinemia' ->

Date index: 2021-01-29
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