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Adhesions
Adhesive bands
Anaemia Addison
Biermer
Congenital
Congenital afibrinogenaemia Deficiency AC globulin
Congenital intrinsic factor deficiency
Deficiency of factor I
Diaphragm
Early congenital syphilis cutaneous
Early congenital syphilitic laryngitis
Fibrin-stabilizing
Fibrinogen
From birth
Hageman
II
Intestine
Labile
Male pelvis
Mesenteric
Mucocutaneous
Oculopathy
Omentum
Osteochondropathy
Pernicious
Pharyngitis
Pneumonia
Proaccelerin
Prothrombin
Rhinitis
Stable
Stomach
Stuart-Prower
V
VII
Visceral
X
XII
XIII

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
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
congenital | from birth
http://users.ugent.be/~rvdstic (...) (...) [HTML]
congénital | présent à la naissance
UGENT - Medical terms -
UGENT - Medical terms -
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http://users.ugent.be/~rvdstic (...) [HTML]
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
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syndrome de McDonough
SNOMEDCT-BE (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def / 715441004
SNOMEDCT-BE (disorder) / 715441004
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https://browser.ihtsdotools.or (...) [HTML]
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
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hypothyroïdie congénitale idiopathique
SNOMEDCT-BE (disorder) / 717334008
SNOMEDCT-BE (disorder) / 717334008
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https://browser.ihtsdotools.or (...) [HTML]
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.
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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
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https://browser.ihtsdotools.or (...) [HTML]
Early congenital syphilis:cutaneous | mucocutaneous | visceral | Early congenital syphilitic:laryngitis | oculopathy | osteochondropathy | pharyngitis | pneumonia | rhinitis
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Late congenital syphilitic interstitial keratitis+ (H19.2*) Late congenital syphilitic oculopathy NEC+ (H58.8*)
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Elliptocytosis (congenital) Ovalocytosis (congenital)(hereditary)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Elliptocytose (congénitale) Ovalocytose (congénitale) (héréditaire)
WORLD HEALTH ORGANIZATION ICD-10: D58.1
WORLD HEALTH ORGANIZATION ICD-10: D58.1
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
Anaemia:Addison | Biermer | pernicious (congenital) | Congenital intrinsic factor deficiency
https://icd.who.int/browse10/2 (...) (...) [HTML]
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
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
IN-CONTEXT TRANSLATIONS


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'Congenital adhesions'

Date index:2020-12-17 -

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