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Neuropathie héréditaire sensitive et autonomique
Neuropathie héréditaire sensitive et autonomique type 1
Neuropathie motrice distale héréditaire type 1
Neuropathie motrice distale héréditaire type Jerash
Neuropathie sensitivo-motrice héréditaire type Okinawa
Neuropathie sensitivomotrice héréditaire de type I
Neuropathie sensitivomotrice héréditaire type 4
Récessive
Syndrome de Nélaton

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

neuropathie sensitivomotrice héréditaire type 4

Refsum's disease
SNOMEDCT-BE (disorder) / 25362006
SNOMEDCT-BE (disorder) / 25362006


neuropathie sensitivomotrice héréditaire de type I

HSMN, type I
SNOMEDCT-BE (disorder) / 398040009
SNOMEDCT-BE (disorder) / 398040009


Maladie de Morvan Neuropathie sensitive héréditaire à transmission:dominante | récessive | Syndrome de Nélaton

Morvan's disease Nelaton's syndrome Sensory neuropathy:dominantly inherited | recessively inherited
WORLD HEALTH ORGANIZATION ICD-10: G60.8
WORLD HEALTH ORGANIZATION ICD-10: G60.8


neuropathie motrice distale héréditaire de l'adulte jeune

Autosomal recessive distal spinal muscular atrophy type 5
SNOMEDCT-BE (disorder) / 771475006
SNOMEDCT-BE (disorder) / 771475006


neuropathie héréditaire sensitive et autonomique

Hereditary sensory and autonomic neuropathy
SNOMEDCT-BE (disorder) / 128205005
SNOMEDCT-BE (disorder) / 128205005


neuropathie héréditaire sensitive et autonomique type 1

Hereditary sensory and autonomic neuropathy type I
SNOMEDCT-BE (disorder) / 397734008
SNOMEDCT-BE (disorder) / 397734008


neuropathie sensitivo-motrice héréditaire type Okinawa

An autosomal dominant form of hereditary motor and sensory neuropathy with dominant proximal involvement. Manifestations include adult-onset proximal neurogenic atrophy, sensory involvement, painful muscle cramps, fasciculations, areflexia, and high
SNOMEDCT-BE (disorder) / 715665006
SNOMEDCT-BE (disorder) / 715665006


neuropathie motrice distale héréditaire type 1

Autosomal dominant distal juvenile spinal muscular atrophy type 1
SNOMEDCT-BE (disorder) / 770630005
SNOMEDCT-BE (disorder) / 770630005


neuropathie motrice distale héréditaire type Jerash

Autosomal recessive distal spinal muscular atrophy type 2
SNOMEDCT-BE (disorder) / 763533003
SNOMEDCT-BE (disorder) / 763533003


neuropathie héréditaire sensitive et autonomique type 1B

Hereditary sensory and autonomic neuropathy type 1B
SNOMEDCT-BE (disorder) / 717825008
SNOMEDCT-BE (disorder) / 717825008




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neuropathie sensitivomotrice héréditaire

Date index:2021-08-30 -

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