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

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

hypogammaglobulinémie à expression variable

médecine > allergologie | biologie > immunologie

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

hypogammaglobulinemia | hypogammaglobulinaemia | agammaglobulineamia

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

agammaglobulinémie

médecine

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

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

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

hypogammaglobulinémie à expression variable

Immunology

Immunologie

http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]

http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]

antibody deficiency syndrome | Bruton disease

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

syndrome par manque d'anticorps

IATE - Health

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

Bruton's type agammaglobulinemia

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

agammaglobulinémie type Bruton

SNOMEDCT-BE (disorder) / 65880007

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

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

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome d'insuffisance antéhypophysaire-déficit immunitaire variable

SNOMEDCT-BE (disorder) / 773664005

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

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

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

syndrome de maladie veino-occlusive hépatique-immunodéficience

SNOMEDCT-BE (disorder) / 724361001

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

Others have searched : bruton disease bruton type agammaglobulinemia bruton's x-linked agammaglobulinemia bruton's agammaglobulinemia bruton's disease bruton's type agammaglobulinemia x-linked agammaglobulinaemia x-linked agammaglobulinemia acquired agammaglobulinemia agammaglobulineamia antibody deficiency syndrome common variable agammaglobulinemia common variable immunodeficiency common variable unclassifiable immunodeficiency Bruton hypogammaglobulinemia

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'Bruton hypogammaglobulinemia'

Date index:2021-05-01 -

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

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