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Autosomal dominant myoglobinuria
Azoturia
Dumb rabies
Enzootic myoglobinuria of horses
Genetic recurrent myoglobinuria
Monday morning disease
Monday morning sickness
Myoglobinuria
NMBA
Neuromuscular blocker
Neuromuscular blocking agent
Paralytic
Paralytic drug
Paralytic flat foot
Paralytic flatfoot
Paralytic hydrophobia
Paralytic mydriasis
Paralytic myoglobinuria
Paralytic rabies
Sullen rabies

Translation of "paralytic myoglobinuria " (English → French) :

azoturia [ paralytic myoglobinuria | Monday morning disease | Monday morning sickness ]

azoturie [ myoglobinurie paralytique | maladie du lundi ]
Horse Husbandry | Horse Racing and Equestrian Sports | Animal Diseases
Élevage des chevaux | Courses hippiques et sports équestres | Maladies des animaux


A rare metabolic myopathy with characteristics of muscle cramping and/or stiffness after exercise (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL

myopathie métabolique par défaut de transport du lactate
SNOMEDCT-BE (especially during heat exposure), post-exertional rhabdomyolysis and myoglobinuria and elevation of serum creatine kinase. Caused by mutation in the SL / 766715000
SNOMEDCT-BE (disorder) / 766715000


paralytic flatfoot [ paralytic flat foot ]

pied plat paralytique
Musculoskeletal System | Symptoms (Medicine)
Appareil locomoteur (Médecine) | Symptômes (Médecine)


paralytic rabies | dumb rabies | sullen rabies | paralytic hydrophobia

rage paralytique | rage muette
médecine > infectiologie
médecine > infectiologie


neuromuscular blocking agent [ NMBA | neuromuscular blocker | paralytic drug | paralytic ]

curarisant [ curare | bloqueur neuromusculaire ]
Nervous System | Muscles and Tendons | Medication
Système nerveux | Muscles et tendons | Médicaments




enzootic myoglobinuria of horses

myoglobinurie insidieuse du cheval | myoglubinurie enzootique des chevaux
médecine > médecine vétérinaire
médecine > médecine vétérinaire


Autosomal dominant myoglobinuria

myoglobinurie autosomique dominante
SNOMEDCT-BE (disorder) / 725903003
SNOMEDCT-BE (disorder) / 725903003


Genetic recurrent myoglobinuria

myoglobinurie récurrente génétique
SNOMEDCT-BE (disorder) / 716721003
SNOMEDCT-BE (disorder) / 716721003


paralytic mydriasis

mydriase paralytique
médecine > sémiologie et pathologie | médecine > ophtalmologie
médecine > sémiologie et pathologie | médecine > ophtalmologie




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'paralytic myoglobinuria'

Date index:2022-08-09 -

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