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Acrochondrohyperplasia
Acromacria
Arachnodactily
CMD
Congenital mesodermal dystrophy
Congenital muscular dystrophy
Congenital muscular dystrophy NOS
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy with hyperlaxity
Disease central core
Dolichostenomelia
Dystrophia mesodermalis congenita
FCMD
Fukuyama-type congenital muscular dystrophy
Hyperchondroplasia
Marfan's abiotrophy
Marfan's dolichostenomely
Marfan's syndrome 1
Marfan-Achard syndrome
Minicore
Multicore
Nemaline
Salih congenital muscular dystrophy
Spider fingers
Streblodactyly

Translation of "Congenital mesodermal dystrophy " (English → French) :

arachnodactily | Marfan's abiotrophy | Marfan's dolichostenomely | Marfan's syndrome 1 | Marfan-Achard syndrome | acrochondrohyperplasia | acromacria | congenital mesodermal dystrophy | dolichostenomelia | dystrophia mesodermalis congenita | hyperchondroplasia | spider fingers | streblodactyly

arachnodactylie | acromacrie | dolichosténomélie de Marfan | hyperchondroplasie | syndrome de Marfan
médecine > anatomopathologie | biologie > embryologie | biologie > génétique
médecine > anatomopathologie | biologie > embryologie | biologie > génétique


congenital muscular dystrophy | CMD [Abbr.]

dystrophie musculaire congénitale | DMC [Abbr.]
IATE - Health
IATE - Health


Fukuyama-type congenital muscular dystrophy | FCMD [Abbr.]

dystrophie musculaire congénitale de Fukuyama
IATE - Health
IATE - Health


Salih congenital muscular dystrophy

myopathie précoce avec cardiomyopathie létale
SNOMEDCT-BE (disorder) / 702343002
SNOMEDCT-BE (disorder) / 702343002


Congenital muscular dystrophy type 1B

dystrophie musculaire congénitale type 1B
SNOMEDCT-BE (disorder) / 764944006
SNOMEDCT-BE (disorder) / 764944006


Congenital muscular dystrophy:NOS | with specific morphological abnormalities of the muscle fibre | Disease:central core | minicore | multicore | Fibre-type disproportion Myopathy:myotubular (centronuclear) | nemaline

Disproportion des types de fibres Dystrophie musculaire congénitale:SAI | avec anomalies morphologiques spécifiques des fibres musculaires | Myopathie:à axe central | à bâtonnets [némaline] | de type: mini-core | multi-core | myotubulaire (centro-nucléaire)
WORLD HEALTH ORGANIZATION ICD-10: G71.2
WORLD HEALTH ORGANIZATION ICD-10: G71.2


Congenital muscular dystrophy with hyperlaxity

dystrophie musculaire congénitale avec hyperlaxité
SNOMEDCT-BE (disorder) / 763314009
SNOMEDCT-BE (disorder) / 763314009




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'Congenital mesodermal dystrophy'

Date index:2024-02-05 -

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