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Dystrophie endothéliale congénitale héréditaire type I
Dystrophie endothéliale congénitale héréditaire type II
Déjerine-Sottas
Hypertrophique de l'enfant
Myopathie à corps d'inclusion héréditaire type 4
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivomotrice héréditaire de type I
Neuropathie sensitivomotrice héréditaire type 4
Syndrome de Roussy-Lévy

Translation of "sensitivomotrice héréditaire type " (French → English) :

neuropathie sensitivomotrice héréditaire type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
Refsum's disease
SNOMEDCT-BE (disorder) / 25362006
SNOMEDCT-BE (disorder) / 25362006
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie sensitivomotrice héréditaire de type I
https://browser.ihtsdotools.or (...) (...) [HTML]
HSMN, type I
SNOMEDCT-BE (disorder) / 398040009
SNOMEDCT-BE (disorder) / 398040009
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
Amyotrophie péronière (type axonal) (type hypertrophique) Maladie de:Charcot-Marie-Tooth | Déjerine-Sottas | Neuropathie:héréditaire motrice et sensorielle, types I-IV | hypertrophique de l'enfant | Syndrome de Roussy-Lévy
https://icd.who.int/browse10/2 (...) (...) [HTML]
Disease:Charcot-Marie-Tooth | Déjerine-Sottas | Hereditary motor and sensory neuropathy, types I-IV Hypertrophic neuropathy of infancy Peroneal muscular atrophy (axonal type)(hypertrophic type) Roussy-Lévy syndrome
WORLD HEALTH ORGANIZATION ICD-10: G60.0
WORLD HEALTH ORGANIZATION ICD-10: G60.0
https://icd.who.int/browse10/2 (...) (...) [HTML]
https://icd.who.int/browse10/2 (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie héréditaire sensitive et autonomique type 1B
https://browser.ihtsdotools.or (...) (...) [HTML]
Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type Jerash
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
neuropathie motrice distale héréditaire type 1
https://browser.ihtsdotools.or (...) (...) [HTML]
Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
myopathie à corps d'inclusion héréditaire type 4
https://browser.ihtsdotools.or (...) (...) [HTML]
A rare non-dystrophic myopathy with characteristics of slowly progressive muscular weakness and atrophy initially involving proximal lower limbs and hip girdle and later on shoulder girdle, proximal upper limbs and axial muscles. Ambulation is usuall
SNOMEDCT-BE (disorder) / 770786001
SNOMEDCT-BE (disorder) / 770786001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
dystrophie endothéliale congénitale héréditaire type I
https://browser.ihtsdotools.or (...) (...) [HTML]
Congenital hereditary endothelial dystrophy type 1
SNOMEDCT-BE (disorder) / 416633008
SNOMEDCT-BE (disorder) / 416633008
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]
dystrophie endothéliale congénitale héréditaire type II
https://browser.ihtsdotools.or (...) (...) [HTML]
Congenital hereditary endothelial dystrophy, 2
SNOMEDCT-BE (disorder) / 417395001
SNOMEDCT-BE (disorder) / 417395001
https://browser.ihtsdotools.or (...) (...) [HTML]
https://browser.ihtsdotools.or (...) [HTML]


Others have searched : déjerine-sottas    syndrome de roussy-lévy    hypertrophique de l'enfant    neuropathie sensitivomotrice héréditaire type    sensitivomotrice héréditaire type    


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sensitivomotrice héréditaire type

Date index:2021-01-28 -

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