About: Dejerine–Sottas disease     Goto   Sponge   NotDistinct   Permalink

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a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting

AttributesValues
rdf:type
description
  • مرض من الأمراض (ar)
  • een neurologische aandoening gekarakteriseerd door schade aan het perifeer zenuwstelsel (nl)
  • hereditäre motorische und sensible Neuropathie (de)
  • neuropathie sensitivo-motrice héréditaire (fr)
  • a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting (en)
health specialty
ICD-10
Mondo ID
DiseasesDB
Mondo ID
health specialty
ICD-10
  • G60.0
Mondo ID
  • MONDO_0007790
DiseasesDB
  • 5821
rdfs:label
  • Dejerine-Sottas-Krankheit (de)
  • Dejerine–Sottas disease (en)
  • Déjerine Sottas syndroom (nl)
  • Maladìa ëd Dejerine-Sottas (pms)
  • Sindrome di Dejerine-Sottas (it)
  • syndrome de Dejerine-Sottas (fr)
  • داء ديجيرين-سوتاس (ar)
skos:prefLabel
  • Dejerine-Sottas-Krankheit (de)
  • Dejerine–Sottas disease (en)
  • Déjerine Sottas syndroom (nl)
  • Maladìa ëd Dejerine-Sottas (pms)
  • Sindrome di Dejerine-Sottas (it)
  • syndrome de Dejerine-Sottas (fr)
  • داء ديجيرين-سوتاس (ar)
name
  • Dejerine-Sottas-Krankheit (de)
  • Dejerine–Sottas disease (en)
  • Déjerine Sottas syndroom (nl)
  • Maladìa ëd Dejerine-Sottas (pms)
  • Sindrome di Dejerine-Sottas (it)
  • syndrome de Dejerine-Sottas (fr)
  • داء ديجيرين-سوتاس (ar)
instance of
instance of
subclass of
subclass of
UniProt disease ID
Orphanet ID
genetic association
GARD rare disease ID
OMIM ID
UniProt disease ID
  • DI-00387
Orphanet ID
  • 64748
genetic association
GARD rare disease ID
  • 9204
OMIM ID
  • 145900
named after
named after
ICD-9 ID
ICD-9 ID
  • 356.0
Commons category
Commons category
  • Dejerine-Sottas disease
skos:altLabel
  • progressive hypertrophic interstitial polyneuropathy of childhood (en)
  • progressieve hypertrophische interstitiële kinder polyneuropathie (nl)
  • Charcot-Marie-Tooth type 3 (en)
  • Charcot-Marie-Tooth type 3 (fr)
  • Dejerine–Sottas neuropathy (en)
  • Dejerine–Sottas syndrome (en)
  • Sindrome di Déjerine-Sottas (it)
  • onion bulb neuropathy (en)
  • hereditary motor and sensory polyneuropathy type III (en)
BabelNet ID
Microsoft Academic ID
BabelNet ID
Microsoft Academic ID
BabelNet ID
  • 03410583n
Microsoft Academic ID
  • 2780818367
WikiProjectMed ID
WikiProjectMed ID
  • Dejerine–Sottas disease
is about of
is genetic association of
is genetic association of
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