Boost Your Productivity !Translate documents (Ms-Word, Ms-Excel, ...) faster and better thanks to artificial intelligence!
https://pro.wordscope.com
https://blog. wordscope .com
Bicuspidie aortique familiale
Dysautonomie familiale
Elliptocytose familiale
Elliptocytose héréditaire
Epilepsie myoclonique bénigne familiale de l'adulte
Lipodystrophie partielle familiale type Köbberling
Urticaire familiale au froid

Translation of "Elliptocytose familiale " (French → English) :

elliptocytose familiale
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary ovalocytosis
SNOMEDCT-BE (disorder) / 191169008
SNOMEDCT-BE (disorder) / 191169008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Elliptocytose héréditaire
https://icd.who.int/browse10/2 (...) (...) [HTML]
Hereditary elliptocytosis
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]
Elliptocytose (congénitale) Ovalocytose (congénitale) (héréditaire)
https://icd.who.int/browse10/2 (...) (...) [HTML]
Elliptocytosis (congenital) Ovalocytosis (congenital)(hereditary)
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]
Fièvre méditerranéenne familiale Néphropathie amyloïde familiale
https://icd.who.int/browse10/2 (...) (...) [HTML]
Familial Mediterranean fever Hereditary amyloid nephropathy
WORLD HEALTH ORGANIZATION ICD-10: E85.0
WORLD HEALTH ORGANIZATION ICD-10: E85.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
lipodystrophie partielle familiale type Köbberling
https://browser.ihtsdotools.or (...) (...) [HTML]
A very rare form of familial partial lipodystrophy of unknown aetiology characterised by loss of adipose tissue that is confined to the limbs and a normal or increased fat distribution of the face, neck, and trunk. Arterial hypertension and diabetes
SNOMEDCT-BE (disorder) / 725035001
SNOMEDCT-BE (disorder) / 725035001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
dilatation idiopathique familiale de l'oreillette droite
https://browser.ihtsdotools.or (...) (...) [HTML]
A rare congenital heart malformation of unknown aetiology that is characterised by an extremely dilated right atrium. It is usually asymptomatic and fortuitously discovered by echocardiography or chest radiography and can be sometimes associated with
SNOMEDCT-BE (disorder) / 716773002
SNOMEDCT-BE (disorder) / 716773002
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
dysautonomie familiale
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type III
SNOMEDCT-BE (disorder) / 29159009
SNOMEDCT-BE (disorder) / 29159009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
epilepsie myoclonique bénigne familiale de l'adulte
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant cortical myoclonus and epilepsy
SNOMEDCT-BE (disorder) / 717225001
SNOMEDCT-BE (disorder) / 717225001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
urticaire familiale au froid
https://browser.ihtsdotools.or (...) (...) [HTML]
Familial cold autoinflammatory syndrome
SNOMEDCT-BE (disorder) / 238687000
SNOMEDCT-BE (disorder) / 238687000
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
bicuspidie aortique familiale
https://browser.ihtsdotools.or (...) (...) [HTML]
Familial bicuspid aortic valve
SNOMEDCT-BE (disorder) / 770435005
SNOMEDCT-BE (disorder) / 770435005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : elliptocytose ovalocytose    elliptocytose héréditaire    fièvre méditerranéenne familiale néphropathie amyloïde familiale    bicuspidie aortique familiale    dysautonomie familiale    elliptocytose familiale    lipodystrophie partielle familiale type köbberling    urticaire familiale au froid    Elliptocytose familiale    


www.wordscope.com (v4.0.br.77)

Elliptocytose familiale

Date index:2020-12-10 -

Pour agences de traduction et traducteurs - For translation agencies & translators

Paris - Brussels - Montreal - Genève - Luxembourg - Madrid

Wordscope - Professional computer-assisted translation tools (CAT tools)