8C20.0

ICD-11 MMS 2026-01

Charcot-Marie-Tooth disease 1 demyelinating

Index terms

  • Charcot-Marie-Tooth disease 1 demyelinating
  • Charcot-Marie-Tooth disease 1 autosomal dominant
  • Charcot-Marie-Tooth disease 1 autosomal dominant due to chromosome 17 duplication
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  • CMT1A - [Charcot-Marie-Tooth disease type 1A]
  • Charcot Marie Tooth disease 1 autosomal dominant secondary to the chromosome 17 duplication
  • Charcot-Marie-Tooth disease type 1A
  • Charcot-Marie-Tooth disease type 1E
  • Charcot-Marie-Tooth disease type 1B
  • Charcot-Marie-Tooth disease type 1C
  • Charcot-Marie-Tooth disease type 1D
  • Charcot-Marie-Tooth disease type 1F
  • Charcot-Marie-Tooth disease 1 autosomal recessive
  • CMT4 - [Charcot-Marie-Tooth disease type 4]
  • Charcot-Marie-Tooth disease type 4
  • Charcot-Marie-Tooth disease - deafness - intellectual deficit
  • Charcot-Marie-Tooth disease type 4A
  • Charcot-Marie-Tooth disease type 4C
  • Charcot-Marie-Tooth disease type 4D
  • Charcot-Marie-Tooth disease type 4E
  • Charcot-Marie-Tooth disease type 4F
  • Charcot-Marie-Tooth disease type 4G
  • Charcot-Marie-Tooth disease type 4H
  • Charcot-Marie-Tooth disease type 4B1
  • Charcot-Marie-Tooth disease type 4B2
  • Charcot-Marie-Tooth disease type 4J
  • X-linked Charcot-Marie-Tooth disease 1 due to mutations in gap junction protein beta 1
  • X-linked Charcot-Marie-Tooth disease 1 secondary to mutations in gap junction protein beta 1
  • Charcot-Marie-Tooth disease 1X, x-linked Charcot-Marie-Tooth disease 1 due to mutations in gap junction protein beta 1
  • Charcot-Marie-Tooth disease 1X, x-linked Charcot-Marie-Tooth disease 1 secondary to mutations in gap junction protein beta 1
  • Hereditary sensorimotor neuropathy with hyperelastic skin

Exclusions from above levels

  • FB56 – neuritis NOS
  • http://id.who.int/icd/entity/114997967 – Injury of nerves or lumbar spinal cord at abdomen, lower back or pelvis level
  • http://id.who.int/icd/entity/1454363907 – Injury of nerves or spinal cord at neck level
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  • NA04 – Injury of cranial nerves
  • NC14 – Injury of nerves at shoulder or upper arm level
  • NC34 – Injury of nerves at forearm level
  • NC55 – Injury of nerves at wrist or hand level
  • NC74 – Injury of nerves at hip or thigh level
  • NC94 – Injury of nerves at lower leg level
  • ND15 – Injury of nerves at ankle or foot level
  • 05 – Endocrine, nutritional or metabolic diseases
  • 18 – Complications of pregnancy, childbirth and the puerperium
  • 19 – Certain conditions originating in the perinatal period
  • 22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

  • 8C20.1 – Charcot-Marie-Tooth disease 2 axonal
  • 8C20.2 – Intermediate Charcot-Marie-Tooth disease
  • 8C20.Y – Other specified hereditary motor and sensory neuropathy
  • 8C20.Z – Hereditary motor and sensory neuropathy, unspecified

Foundation entity

Charcot-Marie-Tooth disease 1 demyelinating – http://id.who.int/icd/entity/1207560843

Part of: 8C20: Hereditary motor and sensory neuropathy › 08: Diseases of the nervous system