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Translation of "congenital adhesions " (English → French) :
TERMINOLOGY
see also In-Context Translations below Adhesions (of):abdominal (wall) | diaphragm | intestine | male pelvis | mesenteric | omentum | stomach | Adhesive bands
Adhérences (de):diaphragmatiques | épiploïques | gastriques | intestinales | mésentériques | paroi abdominale | pelviennes, chez l'homme | Brides d'adhérence
WORLD HEALTH ORGANIZATION ICD-10: K66.0
WORLD HEALTH ORGANIZATION ICD-10: K66.0
congenital | from birth
congénital | présent à la naissance
UGENT - Medical terms -
UGENT - Medical terms -
Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def
syndrome de McDonough
SNOMEDCT-BE (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def / 715441004
SNOMEDCT-BE (disorder) / 715441004
Idiopathic congenital hypothyroidism is a type of primary congenital hypothyroidism whose cause and prevalence are unknown. Clinical manifestations are those of other forms of congenital hypothyroidism. Goiter is always absent. Ultrasound examination
hypothyroïdie congénitale idiopathique
SNOMEDCT-BE (disorder) / 717334008
SNOMEDCT-BE (disorder) / 717334008
A very rare syndrome with characteristics of the association of Mobius syndrome (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic.
syndrome de Moebius-neuropathie axonale-hypogonadisme hypogonadotrope
SNOMEDCT-BE (congenital facial palsy with impaired ocular abduction) with peripheral axonal neuropathy and hypogonadotropic hypogonadism. All of the reported cases were sporadic. / 724174003
SNOMEDCT-BE (disorder) / 724174003
Early congenital syphilis:cutaneous | mucocutaneous | visceral | Early congenital syphilitic:laryngitis | oculopathy | osteochondropathy | pharyngitis | pneumonia | rhinitis
Laryngite | Oculopathie | Ostéochondropathie | Pharyngite | Pneumopathie | Rhinite | syphilitique congénitale précoce | Syphilis congénitale précoce:cutanée | cutanéo-muqueuse | viscérale
WORLD HEALTH ORGANIZATION ICD-10: A50.0
WORLD HEALTH ORGANIZATION ICD-10: A50.0
Late congenital syphilitic interstitial keratitis+ (H19.2*) Late congenital syphilitic oculopathy NEC+ (H58.8*)
Kératite interstitielle syphilitique congénitale tardive+ (H19.2*) Oculopathie syphilitique congénitale tardive NCA+ (H58.8*)
WORLD HEALTH ORGANIZATION ICD-10: A50.3
WORLD HEALTH ORGANIZATION ICD-10: A50.3
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
Elliptocytosis (congenital) Ovalocytosis (congenital)(hereditary)
Elliptocytose (congénitale) Ovalocytose (congénitale) (héréditaire)
WORLD HEALTH ORGANIZATION ICD-10: D58.1
WORLD HEALTH ORGANIZATION ICD-10: D58.1
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
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'congenital adhesions'
Date index:2021-01-30 -
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