8C20.0
category
Charcot-Marie-Tooth disease 1 demyelinating
Also indexed as
CMT1A - [Charcot-Marie-Tooth disease type 1A]CMT4 - [Charcot-Marie-Tooth disease type 4]Charcot Marie Tooth disease 1 autosomal dominant secondary to the chromosome 17 duplicationCharcot-Marie-Tooth disease - deafness - intellectual deficitCharcot-Marie-Tooth disease 1 autosomal dominantCharcot-Marie-Tooth disease 1 autosomal dominant due to chromosome 17 duplicationCharcot-Marie-Tooth disease 1 autosomal recessiveCharcot-Marie-Tooth disease 1 demyelinatingCharcot-Marie-Tooth disease 1X, x-linked Charcot-Marie-Tooth disease 1 due to mutations in gap junction protein beta 1Charcot-Marie-Tooth disease 1X, x-linked Charcot-Marie-Tooth disease 1 secondary to mutations in gap junction protein beta 1Charcot-Marie-Tooth disease type 1ACharcot-Marie-Tooth disease type 1BCharcot-Marie-Tooth disease type 1CCharcot-Marie-Tooth disease type 1DCharcot-Marie-Tooth disease type 1ECharcot-Marie-Tooth disease type 1FCharcot-Marie-Tooth disease type 4Charcot-Marie-Tooth disease type 4ACharcot-Marie-Tooth disease type 4B1Charcot-Marie-Tooth disease type 4B2Charcot-Marie-Tooth disease type 4CCharcot-Marie-Tooth disease type 4DCharcot-Marie-Tooth disease type 4ECharcot-Marie-Tooth disease type 4FCharcot-Marie-Tooth disease type 4GCharcot-Marie-Tooth disease type 4HCharcot-Marie-Tooth disease type 4JHereditary sensorimotor neuropathy with hyperelastic skinX-linked Charcot-Marie-Tooth disease 1 due to mutations in gap junction protein beta 1X-linked Charcot-Marie-Tooth disease 1 secondary to mutations in gap junction protein beta 1