WORDSCOPE MESSAGE : Wordscope Server is currently unavailable (Maintenance) - Please try again in a few minutes !
Boost Your Productivity !Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
Translation of "congénitale " (French → English) :
TERMINOLOGY
see also In-Context Translations below Anomalie congénitale | Anomalies multiples congénitales | Maladie ou lésion congénitale | SAI de l'encéphale
Congenital:anomaly | deformity | disease or lesion | multiple anomalies | NOS of brain
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
tératologique | relatif à l'étude des monstruosités et des anomalies congénitales
teratological | early fetus development-related
UGENT - Medical terms -
UGENT - Medical terms -
cloaque (termerare) | malformation congénitale réalisant une cavité commune dans laquelle s'ouvrent le système uro-génital et la portion terminale du tube digestif. Le système uro-génital et la portion terminale du tube digestif
cloaca | waste passage
UGENT - Medical terms -
UGENT - Medical terms -
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 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
WORLD HEALTH ORGANIZATION ICD-10: D68.2
WORLD HEALTH ORGANIZATION ICD-10: D68.2
Elliptocytose (congénitale) Ovalocytose (congénitale) (héréditaire)
Elliptocytosis (congenital) Ovalocytosis (congenital)(hereditary)
WORLD HEALTH ORGANIZATION ICD-10: D58.1
WORLD HEALTH ORGANIZATION ICD-10: D58.1
Arthropathie+ (M03.1*) | Ostéochondropathie+ (M90.2*) | syphilitique congénitale tardive | Dents de Hutchinson Maladie de Clutton+ (M03.1*) Nez en selle attribuable à la syphilis Syphilis cardio-vasculaire congénitale tardive+ (I98.0*) Triade de Hutchinson
Clutton's joints+ (M03.1*) Hutchinson's:teeth | triad | Late congenital:cardiovascular syphilis+ (I98.0*) | syphilitic:arthropathy+ (M03.1*) | osteochondropathy+ (M90.2*) | Syphilitic saddle nose
WORLD HEALTH ORGANIZATION ICD-10: A50.5
WORLD HEALTH ORGANIZATION ICD-10: A50.5
Anémie (de):Addison | Biermer | pernicieuse (congénitale) | Carence congénitale en facteur intrinsèque
Anaemia:Addison | Biermer | pernicious (congenital) | Congenital intrinsic factor deficiency
WORLD HEALTH ORGANIZATION ICD-10: D51.0
WORLD HEALTH ORGANIZATION ICD-10: D51.0
Laryngite | Oculopathie | Ostéochondropathie | Pharyngite | Pneumopathie | Rhinite | syphilitique congénitale précoce | Syphilis congénitale précoce:cutanée | cutanéo-muqueuse | viscérale
Early congenital syphilis:cutaneous | mucocutaneous | visceral | Early congenital syphilitic:laryngitis | oculopathy | osteochondropathy | pharyngitis | pneumonia | rhinitis
WORLD HEALTH ORGANIZATION ICD-10: A50.0
WORLD HEALTH ORGANIZATION ICD-10: A50.0
Kératite interstitielle syphilitique congénitale tardive+ (H19.2*) Oculopathie syphilitique congénitale tardive NCA+ (H58.8*)
Late congenital syphilitic interstitial keratitis+ (H19.2*) Late congenital syphilitic oculopathy NEC+ (H58.8*)
WORLD HEALTH ORGANIZATION ICD-10: A50.3
WORLD HEALTH ORGANIZATION ICD-10: A50.3
Aplasie de la thyroïde (avec myxœdème) Atrophie congénitale de la thyroïde Hypothyroïdie congénitale SAI
Aplasia of thyroid (with myxoedema) Congenital:atrophy of thyroid | hypothyroidism NOS
WORLD HEALTH ORGANIZATION ICD-10: E03.1
WORLD HEALTH ORGANIZATION ICD-10: E03.1
www.wordscope.com (v4.0.br.77)
congénitale
Date index:2023-02-17 -
Pour agences de traduction et traducteurs - For translation agencies & translators
Paris - Brussels - Montreal - Genève - Luxembourg - Madrid
Wordscope - Professional computer-assisted translation tools (CAT tools)