
CMT2R
Associated Gene
TRIM2
Chromosome
4q31.3
Autosomal Recessive
CMT2R is caused by autosomal recessive mutations in the TRIM . . .
Axonal

CMT2T
Associated Gene
MME
Chromosome
3q25.2
Autosomal Dominant or Recessive
CMT2T is caused by autosomal dominant and autosomal recessiv . . .
Axonal

CMT2V
Associated Gene
NAGLU
Chromosome
17q21.2
Autosomal Dominant
CMT2V is caused by autosomal dominant mutations in the NAGLU . . .
Axonal

CMT2S
Associated Gene
IGHMBP2
Chromosome
11q13.3
Autosomal Recessive
CMT2S is caused by autosomal recessive mutations in the IGHM . . .
Axonal

CMT2U
Associated Gene
MARS1
Chromosome
12q13.3
Autosomal Dominant
CMT2U is caused by autosomal dominant mutations in the MARS1 . . .
Axonal

CMT2W
Associated Gene
HARS1
Chromosome
5q31.3
Autosomal Dominant
CMT2W is caused by autosomal dominant mutations in the HARS1 . . .
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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