8C20.0 Charcot-Marie-Tooth disease 1 demyelinating

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2026-01

synonyms

• 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
• 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

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