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Acquired agammaglobulinemia
Agammaglobulineamia
Antibody deficiency syndrome
Bruton disease
Bruton hypogammaglobulinemia
Bruton type agammaglobulinemia
Bruton's X-linked agammaglobulinemia
Bruton's agammaglobulinemia
Bruton's disease
Bruton's hypogammaglobulinemia
Bruton's type agammaglobulinemia
Common variable agammaglobulinemia
Common variable hypogammaglobulinemia
Common variable immunodeficiency
Common variable unclassifiable immunodeficiency
Congenital hypogammaglobulinaemia
Congenital hypogammaglobulinemia
Hypogammaglobulinaemia
Hypogammaglobulinemia
X-linked agammaglobulinaemia
X-linked agammaglobulinemia
X-linked hypogammaglobulinemia
XLA

Translation of "Bruton hypogammaglobulinemia " (English → French) :

Bruton's agammaglobulinemia [ Bruton's disease | congenital hypogammaglobulinemia | Bruton hypogammaglobulinemia | X-linked hypogammaglobulinemia | Bruton type agammaglobulinemia | X-linked agammaglobulinemia ]

maladie de Bruton [ agammaglobulinémie liée au sexe | agammaglobulinémie liée à l'X | agammaglobulinémie de Bruton ]


Bruton's disease | Bruton's hypogammaglobulinemia | Bruton's X-linked agammaglobulinemia | X-linked agammaglobulinaemia | XLA [Abbr.]

maladie de Bruton


congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia

hypogammaglobulinémie congénitale


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

hypogammaglobulinémie à expression variable


hypogammaglobulinemia | hypogammaglobulinaemia | agammaglobulineamia

agammaglobulinémie


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

hypogammaglobulinémie à expression variable


antibody deficiency syndrome | Bruton disease

syndrome par manque d'anticorps


Bruton's type agammaglobulinemia

agammaglobulinémie type Bruton


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


Syndrome that is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding

syndrome de maladie veino-occlusive hépatique-immunodéficience


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