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ADPCLD - autosomal dominant polycystic liver disease
AIED - Åland Islands eye disease
Border disease-virus
Borna disease-virus
Bovien mucosal disease-virus
Central-core-disease
Congenitale spierdystrofie
Fibre-type disproportion
Gamma heavy chain disease
Minicore disease
Mmu heavy chain disease
Multicore disease
Myopathie
Myotubulair
NNO
Nairobi sheep disease-virus
Nemaline lichaampjes
Ziekte van Franklin

Translation of "Multicore disease " (Dutch → English) :

central-core-disease | congenitale spierdystrofie | NNO | congenitale spierdystrofie | met specifieke morfologische-afwijkingen van spiervezel | fibre-type disproportion | minicore disease | multicore disease | myopathie | myotubulair (centronucleair) | myopathie | nemaline lichaampjes

Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline
WORLD HEALTH ORGANIZATION ICD-10: G71.2
WORLD HEALTH ORGANIZATION ICD-10: G71.2


ziekte van Franklin | gamma heavy chain disease | Mmu heavy chain disease

Franklin's disease
WORLD HEALTH ORGANIZATION ICD-10: C88.2
WORLD HEALTH ORGANIZATION ICD-10: C88.2


ADPCLD - autosomal dominant polycystic liver disease

A genetic disorder with characteristics of the appearance of numerous cysts spread throughout the liver. Women are predominantly affected and have a larger number of cysts than affected males. Cysts are undetectable early in life and usually appear a
SNOMEDCT-BE (disorder) / 716196007
SNOMEDCT-BE (disorder) / 716196007


AIED - Åland Islands eye disease

Aland Islands eye disease
SNOMEDCT-BE (disorder) / 725168006
SNOMEDCT-BE (disorder) / 725168006


Borna disease-virus

Borna disease virus
SNOMEDCT-BE (organism) / 285349002
SNOMEDCT-BE (organism) / 285349002


Border disease-virus

Border disease virus
SNOMEDCT-BE (organism) / 13249005
SNOMEDCT-BE (organism) / 13249005


Nairobi sheep disease-virus

Nairobi sheep disease virus
SNOMEDCT-BE (organism) / 112376002
SNOMEDCT-BE (organism) / 112376002


bovien mucosal disease-virus

Bovine diarrhea virus
SNOMEDCT-BE (organism) / 25018007
SNOMEDCT-BE (organism) / 25018007


ADTKD-MUC1 - MUC1-related autosomal dominant tubulointerstitial kidney disease

Medullary cystic kidney disease 1
SNOMEDCT-BE (disorder) / 726017001
SNOMEDCT-BE (disorder) / 726017001


ADTKD-UMOD - UMOD-related autosomal dominant tubulointerstitial kidney disease

Medullary cystic kidney disease 2
SNOMEDCT-BE (disorder) / 723373006
SNOMEDCT-BE (disorder) / 723373006




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'Multicore disease'

Date index:2022-11-11 -

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