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Anaemia Addison
Biermer
Congenital Factor VIII deficiency
Congenital afibrinogenaemia Deficiency AC globulin
Congenital clotting factor deficiency
Congenital coagulation factor deficiency
Congenital intrinsic factor deficiency
Deficiency of factor I
Fibrin-stabilizing
Fibrinogen
Hageman
II
Labile
Pernicious
Proaccelerin
Prothrombin
Stable
Stuart-Prower
V
VII
X
XII
XIII

Translation of "Congenital intrinsic factor deficiency " (English → French) :

TERMINOLOGY
see also In-Context Translations below
Anaemia:Addison | Biermer | pernicious (congenital) | Congenital intrinsic factor deficiency

Anémie (de):Addison | Biermer | pernicieuse (congénitale) | Carence congénitale en facteur intrinsèque
WORLD HEALTH ORGANIZATION ICD-10: D51.0
WORLD HEALTH ORGANIZATION ICD-10: D51.0


congenital clotting factor deficiency | congenital coagulation factor deficiency

déficit constitutionnel en facteur plasmatique de la coagulation
IATE - Health
IATE - Health


Vitamin B12 deficiency anaemia due to intrinsic factor deficiency

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


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
WORLD HEALTH ORGANIZATION ICD-10: D68.2
WORLD HEALTH ORGANIZATION ICD-10: D68.2


congenital Factor VIII deficiency

déficit congénital en facteur antihémophilique A | déficit congénital en facteur VIII
IATE - Health
IATE - Health


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
SNOMEDCT-BE (disorder) / 718182008
SNOMEDCT-BE (disorder) / 718182008
IN-CONTEXT TRANSLATIONS
Plasma is required to produce vital medicines such as coagulation factor 8 and coagulation factor 7 for haemophiliacs, and immunoglobulins to prevent infection in patients with congenital immune deficiency.

Le plasma sanguin est nécessaire pour la fabrication de médicaments indispensables à la vie, comme par exemple le facteur de coagulation 8 et le facteur de coagulation 7 pour les hémophiles, ou l’immunoglobuline empêchant les infections chez des patients souffrant d’une déficience congénitale des défenses immunitaires.




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'Congenital intrinsic factor deficiency'

Date index:2024-05-12 -

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