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

PMP2-related Charcot-Marie-Tooth disease type 1   1177165005

SNOMED CT code


SNOMED code1177165005
namePMP2-related Charcot-Marie-Tooth disease type 1
statusactive
date introduced2021-10-31
fully specified name(s)Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1 (disorder)
synonyms
  • PMP2-related Charcot-Marie-Tooth disease type 1
  • Peripheral myelin protein 2-related Charcot-Marie-Tooth disease type 1
  • PMP2-related Charcot-Marie-Tooth neuropathy type 1
  • PMP2-related hereditary motor and sensory neuropathy type 1
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
                PMP2-related Charcot-Marie-Tooth disease type 1   1177165005

ancestors
sorted most to least specific
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