
CMT2E
Associated Gene
NEFL
Chromosome
8p21.2
Autosomal Dominant
CMT2E is caused by autosomal dominant mutations in the NEFL . . .
Axonal

CMT2F
Associated Gene
HSPB1
Chromosome
7q11.23
Autosomal Dominant
CMT2F is caused by autosomal dominant mutations in the HSPB1 . . .
Axonal

CMT2J
Associated Gene
MPZ
Chromosome
1q23.3
Autosomal Dominant
CMT2J is caused by autosomal dominant mutations in the MPZ g . . .
Axonal

CMT2EE
Associated Gene
MPV17
Chromosome
2p23.3
Autosomal Recessive
CMT2EE is caused by autosomal recessive mutations in the MPV . . .
Axonal

CMT2I
Associated Gene
MPZ
Chromosome
1q23.3
Autosomal Dominant
CMT2I is caused by autosomal dominant mutations in the MPZ g . . .
Axonal

CMT2K
Associated Gene
GDAP1
Chromosome
8q21.11
Autosomal Dominant or Recessive
CMT2K is caused by autosomal dominant and autosomal recessiv . . .
Axonal

CMT
Type 2
Charcot Marie Tooth Disease
Type 2
This catalog of the Type 2 CMT subtypes represents the current publicly available information for the various subtypes of CMT2. This catalog is comprised of information from several publicly available reputable sources, and each listing includes links to those sources.
CMT Type 2 is an axonal peripheral polyneuropathy and can be autosomal dominant or autosomal recessive in inheritance. The subtypes of CMT2 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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