Hereditary sensory-motor neuropathy, type I   398040009

SNOMED CT code


SNOMED code398040009
nameHereditary sensory-motor neuropathy, type I
statusactive
date introduced2003-07-31
fully specified name(s)Charcot-Marie-Tooth disease, type I (disorder)
synonyms
  • Charcot-Marie-Tooth disease, type I
  • Hereditary sensory-motor neuropathy, type I
  • Peroneal muscular atrophy of demyelinating type
  • Inherited dominant hypertrophic neuropathy
  • Hereditary motor and sensory neuropathy type I
  • Charcot-Marie-Tooth disease of demyelinating type
  • HSMN, type I
  • Charcot Marie Tooth disease, type 1
attributes - group1
Finding sitePeripheral nervous system structure   3058005
parents
  • Autosomal dominant hereditary disorder   11164009
  • Hereditary motor and sensory neuropathy   398100001
children
  • Charcot-Marie-Tooth disease type ID   719979008
  • Charcot-Marie-Tooth disease type IE   715666007
  • Charcot-Marie-Tooth disease type IF   719980006
  • Charcot-Marie-Tooth disease, type IA   40632002
  • Charcot-Marie-Tooth disease, type IB   42986003
  • Charcot-Marie-Tooth disease, type IC   4183003
  • PMP2-related Charcot-Marie-Tooth disease type 1   1177165005
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              Hereditary sensory-motor neuropathy, type I   398040009

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
                Hereditary sensory-motor neuropathy, type I   398040009

ancestors
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