CMT
Type 1
Charcot Marie Tooth Disease
Type 1
This catalog of the Type 1 CMT subtypes represents the current publicly available information for the various subtypes of CMT1. This catalog is comprised of information from several publicly available reputable sources, and each listing includes links to those sources.
CMT Type 1 is a demyelinating peripheral polyneuropathy and is autosomal dominant in inheritance. The subtypes of CMT1 each fit this description.
Every effort is made to provide the most accurate and up-to-date information. However, CMT subtype names can change at any time and without notice. Therefore, the accuracy of this catalog cannot be guaranteed.
The information provided in this catalog is provided for reference and informational purposes only. The information provided is not intended to diagnose any medical condition anybody might have, and this catalog should not be construed as medical advice. Always consult with a qualified physician or healthcare provider and follow their guidance.
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PMP22 (Duplication)
CMT1A
Chromosome
17p.12-p11.2
Associated Gene
Autosomal Dominant
CMT1A is caused by a duplication of the PMP22 gene. Instead . . .
Demyelinating
LITAF
CMT1C
Chromosome
16p13.13
Associated Gene
Autosomal Dominant
CMT1C is caused by autosomal dominant mutations in the LITAF . . .
Demyelinating
PMP22 (Point Mutation)
CMT1E
Chromosome
17p12
Associated Gene
Autosomal Dominant
CMT1E is caused by autosomal dominant mutations in the PMP22 . . .
Demyelinating
MPZ
CMT1B
Chromosome
1q23.3
Associated Gene
Autosomal Dominant
CMT1B is caused by autosomal dominant mutations in the MPZ g . . .
Demyelinating
EGR2
CMT1D
Chromosome
10q21.3
Associated Gene
Autosomal Dominant
CMT1D is caused by autosomal dominant mutations in the EGR2 . . .
Demyelinating
NEFL
CMT1F
Chromosome
8p21.2
Associated Gene
Autosomal Dominant
CMT1F is caused by autosomal dominant mutations in the NEFL . . .
Demyelinating