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

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Charcot-Marie-Tooth disease 1 demyelinating
Charcot-Marie-Tooth disease 1 autosomal dominant
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
Charcot-Marie-Tooth disease type 4
CMT4 - [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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