Déjérine-Sottas disease   111499002

SNOMED CT code


SNOMED code111499002
nameDéjérine-Sottas disease
statusactive
date introduced2002-01-31
fully specified name(s)Déjérine-Sottas disease (disorder)
synonyms
  • Hypertrophic hereditary neuropathy
  • Hereditary motor and sensory neuropathy type III
  • Hypertrophic demyelinative neuropathy of infancy
  • Déjérine-Sottas disease
  • Hereditary sensory-motor neuropathy, type III
  • Hereditary hypertrophic neuropathy
  • Dejerine-Sottas disease
  • Progressive hypertrophic interstitial neuropathy
  • Hereditary motor and sensory neuropathy, type III
  • HSMN III
  • HMSN III
  • Charcot-Marie-Tooth disease type 3
attributes - group1
Finding sitePeripheral nerve structure   84782009
Associated morphologyRemyelination   30321009
attributes - group2
Finding sitePeripheral nerve structure   84782009
Associated morphologyHypertrophy   56246009
attributes - group3
Finding sitePeripheral nerve structure   84782009
Associated morphologySegmental demyelination   8723003
parents
  • Hypertrophic interstitial neuropathy   18708008
  • Hereditary motor and sensory neuropathy   398100001
childrenRoussy-Levy syndrome   307540002  removed: 2009-07-31
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Peripheral demyelinating neuropathy   23414001
          Hypertrophic interstitial neuropathy   18708008
            Déjérine-Sottas disease   111499002

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Disorder of nervous system   118940003
          Hereditary disorder of nervous system   363235000
            Hereditary peripheral neuropathy   65017003
              Hereditary motor and sensory neuropathy   398100001
                Déjérine-Sottas disease   111499002

ancestors
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