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Antibody deficiency syndrome
Bruton
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
Congenital hypogammaglobulinaemia
Congenital hypogammaglobulinemia
X-linked agammaglobulinaemia
X-linked agammaglobulinemia
X-linked hypogammaglobulinemia
XLA

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

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

maladie de Bruton
IATE - Health
IATE - Health


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 ]
Immunology
Immunologie


congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia

hypogammaglobulinémie congénitale
IATE - Health
IATE - Health


antibody deficiency syndrome | Bruton disease

syndrome par manque d'anticorps
IATE - Health
IATE - Health


Bruton's type agammaglobulinemia

agammaglobulinémie type Bruton
SNOMEDCT-BE (disorder) / 65880007
SNOMEDCT-BE (disorder) / 65880007


Autosomal recessive agammaglobulinaemia (Swiss type) X-linked agammaglobulinaemia [Bruton] (with growth hormone deficiency)

Agammaglobulinémie:autosomique récessive (type suisse) | liée au chromosome X [Bruton] (avec déficit de l'hormone de croissance)
WORLD HEALTH ORGANIZATION ICD-10: D80.0
WORLD HEALTH ORGANIZATION ICD-10: D80.0


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
SNOMEDCT-BE (disorder) / 724361001
SNOMEDCT-BE (disorder) / 724361001


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




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Bruton's hypogammaglobulinemia

Date index:2022-09-10 -

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