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disease > genetic disease > hereditary disease > Dejerine-Sottas neuropathy
disease > nervous system diseases > peripheral nerve disease > Dejerine-Sottas neuropathy
disease > immunopathology > inflammation > nevritis > Dejerine-Sottas neuropathy
disease > nervous system diseases > neuropathy > nevritis > Dejerine-Sottas neuropathy

Terme préférentiel

Dejerine-Sottas neuropathy  

Définition

  • Dejerine–Sottas disease, also known as, Dejerine–Sottas neuropathy, progressive hypertrophic interstitial polyneuropathy of childhood and onion bulb neuropathy (and, hereditary motor and sensory polyneuropathy type III and Charcot–Marie–Tooth disease type 3), is a hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting. (Wikipedia)

Concept générique

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URI

http://data.loterre.fr/ark:/67375/VH8-HKGCMTHZ-W

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