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Alzheimer's disease
Basedow disease
Basedow's disease
Basedow's syndrome
Begbie's disease
Bulbospinal paralysis
Diffuse toxic goiter
Erb disease
Erb muscular dystrophy
Erb's disease
Erb's palsy
Erb-Duchenne palsy
Erb-Goldflam disease
Erb-Goldflam syndrome
Erb-Landouzy disease
Erb-Oppenheim-Goldflam syndrome
Exophthalmic goiter
Flajani's disease
Flajani-Basedow syndrome
Gilles de la Tourette's disease
Gilles de la Tourette's disorder
Gilles de la Tourette's syndrome
Goldflam's disease
Goldflam-
Graves disease
Graves' disease
Guinon's disease
Hoppe-Goldflam syndrome
Idiopathic muscular atrophy
MG
Maladie des tics
Marsh's disease
Myasthenia gravis
Myasthenia pseudoparalytica
Myodystrophia
Paget disease
Paget disease of the breast
Paget disease of the nipple
Paget's disease
Paget's disease of the breast
Paget's disease of the nipple
Parry's disease
Progressive bulbar paralysis
Progressive muscular dystrophy
Struma exophthalmica
Tic de Guinon
Tourette syndrome
Tourette's disease
Tourette's syndrome
Von Basedow disease
Wilks symptom complex
Wilks syndrome

Translation of "erb's disease " (English → French) :

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


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


Graves' disease [ Graves disease | Basedow's disease | Basedow disease | von Basedow disease | Basedow's syndrome | exophthalmic goiter | diffuse toxic goiter | struma exophthalmica | Flajani's disease | Flajani-Basedow syndrome | Parry's disease | Marsh's disease | Begbie's disease ]

maladie de Basedow [ maladie de Graves | goitre exophtalmique | maladie de Parry | maladie de Flajani ]
Hypophysis | Human Diseases - Various
Hypophyse | Maladies humaines diverses


Erb's palsy [ Erb-Duchenne palsy ]

paralysie radiculaire supérieure [ paralysie de Duchenne-Erb ]
Nervous System
Système nerveux


Paget's disease of the breast | Paget disease of the breast | Paget's disease of the nipple | Paget disease of the nipple | Paget's disease | Paget disease

maladie de Paget du mamelon | maladie de Paget du sein | maladie de Paget mammaire | maladie cutanée de Paget | maladie de Paget
médecine > dermatologie | médecine > oncologie
médecine > dermatologie | médecine > oncologie


Gilles de la Tourette's syndrome | Gilles de la Tourette's disease | maladie des tics | tic de Guinon | Gilles de la Tourette's disorder | Tourette's disease | Tourette's syndrome | Tourette syndrome | Guinon's disease

syndrome de Gilles de la Tourette | SGT | maladie de Gilles de la Tourette | maladie des tics | syndrome de la Tourette
médecine > psychiatrie | psychologie
médecine > psychiatrie | psychologie


Alzheimer's disease | alzheimer's disease [ AD ]

maladie d'Alzheimer | alzheimer [ MA ]
Medicine & biology
Sciences médicales et biologiques | Santé publique (Sciences médicales et biologiques)


Erb muscular dystrophy

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


Disease with characteristics of the adult-onset (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo

ataxie spinocérébelleuse type 38
SNOMEDCT-BE (average age 40 years) of truncal ataxia, gait disturbance and gaze-evoked nystagmus. The disease is slowly progressive with dysarthria and limb ataxia following. Additional manifestations include diplo / 734021001
SNOMEDCT-BE (disorder) / 734021001




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erb's disease

Date index:2022-05-06 -

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