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

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

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

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

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

Anaemia:haemolytic nonspherocytic (hereditary), type II | hexokinase deficiency | pyruvate kinase [PK] deficiency | triose-phosphate isomerase deficiency

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Anémie (due à):déficit en:hexokinase | pyruvate kinase [PK] | triose-phosphate isomérase | hémolytique non sphérocytaire (héréditaire), type II

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

Anémie par carence en vitamine B12 due à une carence en facteur intrinsèque

https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]

https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]

CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

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

acidurie 3-méthylglutaconique type 7

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

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

D'autres ont cherché : g6pd deficiency pnp deficiency purine nucleoside phosphorylase congenital antithrombin iii deficiency congenital deficiency of antithrombin iii deficiency deficiency disease g-6-p-d deficiency glucose 6-dehydrogenase deficiency glucose-6-phosphate dehydrogenase deficiency hexokinase deficiency inherited antithrombin iii deficiency inherited deficiency in at iii nutrition deficiency disease nutritional deficiency disease purine nucleoside phosphorylase deficiency pyruvate kinase triose-phosphate isomerase deficiency PNP deficiency

datacenter (1): www.wordscope.fr (v4.0.br)

'PNP deficiency' ->

Date index: 2022-01-23