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Chronic congestive splenomegaly
Congenital
Cyclic
Drug-induced
Neutropenic disorder
Neutropenic fever
Neutropenic splenomegaly
Periodic
Spleen enlargement
Splenic
Splenomegaly
Splenomegaly associated with AIDS
Toxic

Translation of "Neutropenic splenomegaly " (English → French) :

Agranulocytic angina Infantile genetic agranulocytosis Kostmann's disease Neutropenia:NOS | congenital | cyclic | drug-induced | periodic | splenic (primary) | toxic | Neutropenic splenomegaly

Agranulocytose génétique infantile Angine agranulocytaire Neutropénie:SAI | congénitale | cyclique | médicamenteuse | périodique | splénique (primaire) | toxique | Splénomégalie neutropénique Syndrome de Kostmann
WORLD HEALTH ORGANIZATION ICD-10: D70
WORLD HEALTH ORGANIZATION ICD-10: D70


splenomegaly | spleen enlargement

splénomegalie | augmentation du volume de la rate
UGENT - Medical terms -
UGENT - Medical terms -


Neutropenic fever

neutropénie fébrile
SNOMEDCT-BE (disorder) / 409089005
SNOMEDCT-BE (disorder) / 409089005


Neutropenic disorder

trouble neutropénique
SNOMEDCT-BE (disorder) / 303011007
SNOMEDCT-BE (disorder) / 303011007


A rare disorder with characteristics of sclerosis of the intrahepatic portal veins, non-cirrhotic portal hypertension, asymptomatic splenomegaly and recurrent variceal bleeding. Most commonly, the condition is detected in investigating a fortuitous f

veinopathie portale oblitérative
SNOMEDCT-BE (disorder) / 718096004
SNOMEDCT-BE (disorder) / 718096004


Optic nerve oedema, splenomegaly syndrome

syndrome d'oedème du nerf optique-splénomégalie
SNOMEDCT-BE (disorder) / 771471002
SNOMEDCT-BE (disorder) / 771471002


Chronic congestive splenomegaly

Splénomégalie congestive chronique
WORLD HEALTH ORGANIZATION ICD-10: D73.2
WORLD HEALTH ORGANIZATION ICD-10: D73.2


O/E - moderate splenomegaly

à l'examen : splénomégalie modérée
SNOMEDCT-CA (trouble) / 164165007
SNOMEDCT-CA (trouble) / 164165007


Splenomegaly associated with AIDS

splénomégalie associée au SIDA
SNOMEDCT-CA (trouble) / 422260007
SNOMEDCT-CA (trouble) / 422260007


A rare genetic disorder with characteristics of lymphadenopathy and/or splenomegaly and recurrent infections due to herpes viruses. Prevalence of this disorder is not known. It is extremely rare with four individuals in one family identified to date.

syndrome lymphoprolifératif auto-immun avec infections virales récurrentes
SNOMEDCT-BE (disorder) / 722290008
SNOMEDCT-BE (disorder) / 722290008




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'Neutropenic splenomegaly'

Date index:2023-05-08 -

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