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

Charcot-Marie-Tooth disease type ID   719979008

SNOMED CT code


SNOMED code719979008
nameCharcot-Marie-Tooth disease type ID
statusactive
date introduced2017-01-31
fully specified name(s)Charcot-Marie-Tooth disease type ID (disorder)
synonyms
  • Charcot-Marie-Tooth disease type ID
  • Charcot-Marie-Tooth disease type 1D
attributes - group1
Finding sitePeripheral nervous system structure   3058005
parentsHereditary sensory-motor neuropathy, type I   398040009
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
                Charcot-Marie-Tooth disease type ID   719979008

ancestors
sorted most to least specific
cpt crosswalks

Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts.  Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.

Access to this feature is available in the following products:
  • CPT® to SNOMED Crosswalks

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