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Congenital antithrombin III deficiency
Congenital deficiency of antithrombin III
Deficiency
Deficiency disease
G-6-p-d deficiency
G6PD 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
PK
PNP
PNP deficiency
Purine nucleoside phosphorylase
Purine nucleoside phosphorylase deficiency
Pyruvate kinase
Triose-phosphate isomerase deficiency

Translation of "PNP deficiency " (English → French) :

PNP deficiency
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
déficit en PNP (purine nucléoside phosphorylase)
SNOMEDCT-BE (disorder) / 60743005
SNOMEDCT-BE (disorder) / 60743005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
purine nucleoside phosphorylase deficiency | PNP deficiency
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
déficit en purine nucléoside phosphorylase | déficit en purine-nucléoside phosphorylase | déficit en PNP
médecine > sémiologie et pathologie | biologie > immunologie | biologie > génétique
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]
Purine nucleoside phosphorylase [PNP] deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Déficit en purine nucléoside phosphorylase [PNP]
WORLD HEALTH ORGANIZATION ICD-10: D81.5
WORLD HEALTH ORGANIZATION ICD-10: D81.5
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
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
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
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]
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]
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
WORLD HEALTH ORGANIZATION ICD-10: D55.2
WORLD HEALTH ORGANIZATION ICD-10: D55.2
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
WORLD HEALTH ORGANIZATION ICD-10: D51.0
WORLD HEALTH ORGANIZATION ICD-10: D51.0
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
SNOMEDCT-BE (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency / 764860006
SNOMEDCT-BE (disorder) / 764860006
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


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'PNP deficiency'

Date index:2023-07-25 -

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