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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

Traduction de «PNP deficiency » (Anglais → Français) :

PNP deficiency

déficit en PNP (purine nucléoside phosphorylase)


purine nucleoside phosphorylase deficiency | PNP deficiency

déficit en purine nucléoside phosphorylase | déficit en purine-nucléoside phosphorylase | déficit en PNP


Purine nucleoside phosphorylase [PNP] deficiency

Déficit en purine nucléoside phosphorylase [PNP]


G6PD deficiency | g-6-p-d deficiency | glucose 6-dehydrogenase deficiency | glucose-6-phosphate dehydrogenase deficiency

déficit en G6PD | déficit en glucose-6-phosphate-déshydrogénase


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

déficit congénital en antithrombine III


deficiency disease | nutrition deficiency disease | nutritional deficiency disease

maladie de carence | maladie par carence alimentaire


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

obésité par déficit du récepteur de la mélanocortine 4


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

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


Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

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


CLBP (ClpB homolog, mitochondrial AAA ATPase chaperonin) deficiency

acidurie 3-méthylglutaconique type 7


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