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Bulbospinal paralysis
Bückler's type II corneal dystrophy
DMD
Duchenne disease
Duchenne dystrophy
Duchenne muscular dystrophy
Duchenne type muscular dystrophy
Duchenne's muscular dystrophy
Duchenne-Griesinger disease
Dystrophy
Erb atrophy
Erb disease
Erb dystrophy
Erb muscular dystrophy
Erb's disease
Erb-Goldflam disease
Erb-Goldflam syndrome
Erb-Landouzy disease
Erb-Oppenheim-Goldflam syndrome
Fehr's spotted corneal dystrophy
Goldflam's disease
Goldflam-
Groenouw type II corneal dystrophy
Groenouw's macular type II corneal dystrophy
Hoppe-Goldflam syndrome
Idiopathic muscular atrophy
Limb-girdle dystrophy
MG
Macular corneal dystrophy
Macular dystrophy
Meryon's disease
Muscular dystrophy - Duchenne type
Myasthenia gravis
Myasthenia pseudoparalytica
Myodystrophia
Progressive bulbar paralysis
Progressive muscular dystrophy
Pseudohypertrophic muscular dystrophy
Wilks symptom complex
Wilks syndrome
Zimmerlin atrophy

Translation of "erb dystrophy " (English → French) :

Duchenne muscular dystrophy [ Duchenne type muscular dystrophy | Duchenne dystrophy | Duchenne disease | Erb dystrophy | Duchenne-Griesinger disease | Zimmerlin atrophy | Erb atrophy ]

maladie de Duchenne de Boulogne
Muscles and Tendons | Symptoms (Medicine)
Muscles et tendons | Symptômes (Médecine)


progressive muscular dystrophy | Erb-Landouzy disease | Erb's disease | idiopathic muscular atrophy | myodystrophia

myopathie primitive progressive | dystrophie musculaire progressive | myopathie atrophique progressive | amyotrophie primitive progressive | amyotrophie progressive | atrophie musculaire progressive
médecine
médecine


macular corneal dystrophy [ macular dystrophy | Groenouw's macular type II corneal dystrophy | Groenouw type II corneal dystrophy | Bückler's type II corneal dystrophy | Fehr's spotted corneal dystrophy ]

dystrophie maculaire [ dystrophie de Groenouw type II ]
Visual Disorders
Troubles de la vision


Erb muscular dystrophy

dystrophie musculaire des ceintures d'Erb
SNOMEDCT-BE (disorder) / 78468005
SNOMEDCT-BE (disorder) / 78468005


Duchenne muscular dystrophy | Duchenne type muscular dystrophy | Duchenne's muscular dystrophy | Meryon's disease | Muscular dystrophy - Duchenne type | pseudohypertrophic muscular dystrophy | DMD [Abbr.]

dystrophie musculaire de Duchenne | myopathie de Duchenne | myopathie primitive progressive pseudo-hypertrophique type Duchenne-Griesinger | myopathie pseudo-hypertrophique de Duchenne | DMD [Abbr.]
IATE - Health
IATE - Health


myasthenia gravis [ MG | Erb disease | progressive bulbar paralysis | Erb-Goldflam syndrome | myasthenia pseudoparalytica | Erb-Oppenheim-Goldflam syndrome | Erb-Goldflam disease | bulbospinal paralysis | Goldflam's disease | Hoppe-Goldflam syndrome | Wilks symptom complex | Wilks syndrome | Goldflam- ]

myasthénie [ myasthénie grave | syndrome d'Erb-Goldflam | paralysie bulbo-spinale | myasthénie grave pseudo-paralytique | syndrome de Hoppe-Goldflam | syndrome d'Erb | syndrome d'Erb-Oppenheim-Goldflam ]
Nervous System
Système nerveux


Erb-Goldflam disease

myasthénie grave
SNOMEDCT-BE (disorder) / 91637004
SNOMEDCT-BE (disorder) / 91637004


limb-girdle dystrophy

dystrophie scapulo-humérale | myopathie scapulo-humérale
médecine
médecine


dystrophy

dystrophie
médecine > pathologie dentaire
médecine > pathologie dentaire


A subtype of junctional epidermolysis bullosa (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge

epidermolyse bulleuse jonctionnelle type non-Herlitz
SNOMEDCT-BE (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A ge / 724225008
SNOMEDCT-BE (disorder) / 724225008




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'erb dystrophy'

Date index:2021-11-20 -

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