
CMT2L
Associated Gene
HSPB8
Chromosome
12q24.23
Autosomal Dominant
CMT2L is caused by autosomal dominant mutations in the HSPB8 . . .
Axonal

CMT2N
Associated Gene
AARS1
Chromosome
16q22.1
Autosomal Dominant
CMT2N is caused by autosomal dominant mutations in the AARS1 . . .
Axonal

CMT2P
Associated Gene
LRSAM1
Chromosome
9q33.3-q34.1
Autosomal Dominant or Recessive
CMT2P is caused by autosomal dominant and autosomal recessiv . . .
Axonal

CMT2M
Associated Gene
DNM2
Chromosome
19p13.2
Autosomal Dominant
CMT2M is caused by autosomal dominant mutations in the DNM2 . . .
Axonal

CMT2O
Associated Gene
DYNC1H1
Chromosome
14q32.31
Autosomal Dominant
CMT2O is caused by autosomal dominant mutations in the DYNC1 . . .
Axonal

CMT2Q
Associated Gene
DHTKD1
Chromosome
10p14
Autosomal Dominant
CMT2Q is caused by autosomal dominant mutations in the DHTKD . . .
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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