haemolytic anaemia secondary to G6PD deficiency | haemolytic anaemia secondary to glucose-6-phosphate dehydrogenase deficiency | hemolytic anemia secondary to G6PD deficiency | hemolytic anemia secondary to glucose-6-phosphate dehydrogenase deficiency

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

anémie hémolytique par déficit en G6PD

IATE - Health

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

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

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

maladie d'Andersen [ glycogénose musculaire type IV ]

Endocrine System and Metabolism | Liver and Biliary Ducts

Systèmes endocrinien et métabolique | Foie et voies biliaires

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

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

congenital antithrombin III deficiency | congenital deficiency of antithrombin III | inherited antithrombin III deficiency | inherited deficiency in AT III

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

déficit congénital en antithrombine III

médecine > anatomopathologie | médecine > hématologie et sérologie

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

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

deficiency disease | nutrition deficiency disease | nutritional deficiency disease

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

maladie de carence | maladie par carence alimentaire

médecine > diététique et nutrition

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

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

secondary granule deficiency | specific granule deficiency | neutrophil specific granule deficiency

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

déficit en granules secondaires

médecine > sémiologie et pathologie | biologie > immunologie | biologie > génétique

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

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

Melanocortin 4 receptor (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child

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

obésité par déficit du récepteur de la mélanocortine 4

SNOMEDCT-BE (MC4R) deficiency is the commonest form of monogenic obesity identified so far. MC4R deficiency is characterized by severe obesity, an increase in lean body mass and bone mineral density, increased linear growth in early child / 717269008

SNOMEDCT-BE (disorder) / 717269008

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

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

Others have searched : andersen disease andersen's disease g6pd deficiency gsd iv najjar-andersen syndrome amylopectinosis amylopectinosis brancher deficiency apertura thoracis inferior apertura thoracis superior brancher deficiency brancher enzyme deficiency congenital antithrombin iii deficiency congenital deficiency of antithrombin iii deficiency disease deficiency in thorax familia g-6-p-d deficiency glucose 6-dehydrogenase deficiency glucose-6-phosphate dehydrogenase deficiency glycogen storage disease type iv glycogenosis iv inferior aperture of thorax inferior thoracic aperture inferior thoracic opening inherited antithrombin iii deficiency inherited deficiency in at iii inlet of thorax lower thoracic opening neutrophil specific granule deficiency nutrition deficiency disease nutritional deficiency disease outlet of thorax secondary granule deficiency specific granule deficiency superior aperture of thorax superior thoracic aperture superior thoracic opening thoracic inlet thoracic outlet upper thoracic opening

www.wordscope.com (v4.0.br.77)

'deficiency in thorax'

Date index:2021-12-10 -

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Translation of "deficiency in thorax " (English → French) :

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