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Congenital Factor VIII deficiency
Congenital afibrinogenaemia Deficiency AC globulin
Congenital antithrombin III deficiency
Congenital atransferrinemia
Congenital clotting factor deficiency
Congenital coagulation factor deficiency
Congenital deficiency of antithrombin III
Congenital lactase deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
Hageman
II
Inherited antithrombin III deficiency
Inherited deficiency in AT III
Labile
Lactase deficiency
Proaccelerin
Prothrombin
Secondary lactase deficiency
Stable
Stuart-Prower
Transferrin deficiency syndrome
V
VII
X
XII
XIII

Traduction de «Congenital lactase deficiency » (Anglais → Français) :

Congenital lactase deficiency

Déficit congénital en lactase


lactase deficiency

déficience en lactase [ carence en lactase | insuffisance en lactase ]




Secondary lactase deficiency

ficit secondaire en lactase


Congenital afibrinogenaemia Deficiency:AC globulin | proaccelerin | Deficiency of factor:I [fibrinogen] | II [prothrombin] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [fibrin-stabilizing] | Dysfibrinogenaemia (congenital) Hypoproconvertinaemia Owren's disease

Afibrinogénémie congénitale Carence en:AC-globuline | proaccélérine | Carence en facteur:I [fibrinogène] | II [prothrombine] | V [labile] | VII [stable] | X [Stuart-Prower] | XII [Hageman] | XIII [stabilisant de la fibrine] | Disfibrinogénémie (congénitale) Hypoproconvertinémie Maladie de Owren


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

déficit congénital en antithrombine III


congenital clotting factor deficiency | congenital coagulation factor deficiency

déficit constitutionnel en facteur plasmatique de la coagulation


congenital Factor VIII deficiency

déficit congénital en facteur antihémophilique A | déficit congénital en facteur VIII


congenital atransferrinemia | transferrin deficiency syndrome

manque congénital de transferrine


Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t

déficits hypohysaires multiples de cause génétique identifée


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