
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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PMP2
CMT1G
Chromosome
8q21.13
Associated Gene
Autosomal Dominant
CMT1G is caused by mutations in the PMP2 gene. Not to be con . . .
Demyelinating

PMP22 (Usually a Deletion)
HNPP
Chromosome
17p.12-p11.2
Associated Gene
Autosomal Dominant
HNPP is the acronym for Hereditary Neuropathy with liability . . .
Demyelinating