OMOP Concept 4009656

Déjérine-Sottas disease

StandardConditionSNOMED111499002Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

4 source codes normalize to Déjérine-Sottas disease via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Déjérine-Sottas disease across source vocabularies.

  • Charcot-Marie-Tooth disease type 3
  • Dejerine-Sottas disease
  • Déjérine-Sottas disease (disorder)
  • enfermedad de Charcot-Marie-Tooth tipo 3
  • enfermedad de Dejerine - Sottas
  • enfermedad de Déjérine - Sottas
  • enfermedad de Déjérine - Sottas (trastorno)
  • Hereditary hypertrophic neuropathy
  • Hereditary motor and sensory neuropathy type III
  • Hereditary motor and sensory neuropathy, type III
  • Hereditary sensory-motor neuropathy, type III
  • HMSN III
  • HSMN III
  • Hypertrophic demyelinative neuropathy of infancy
  • Hypertrophic hereditary neuropathy
  • neuropatía desmielinizante hipertrófica de la lactancia
  • neuropatía hipertrófica hereditaria
  • neuropatía intersticial hipertrófica progresiva
  • neuropatía sensitivomotora hereditaria, tipo III
  • neuropatía sensoriomotriz hereditaria, tipo III
  • Progressive hypertrophic interstitial neuropathy

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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