CMT2A
Associated Gene
MFN2
Chromosome
1p36.22
Autosomal Dominant
CMT2A is caused by autosomal dominant mutations in the MFN2 . . .
Axonal
CMT2B
Associated Gene
RAB7
Chromosome
3q21.3
Autosomal Dominant
CMT2B is caused by autosomal dominant mutations in the RAB7 . . .
Axonal
CMT2B2
Associated Gene
MED25
Chromosome
19q13.33
Autosomal Recessive
CMT2B2 is caused by autosomal recessive mutations in the MED . . .
Axonal
CMT2A2B
Associated Gene
MFN2
Chromosome
1p36.22
Autosomal Recessive
CMT2A2B is caused by autosomal recessive mutations in the MF . . .
Axonal
CMT2B1
Associated Gene
LMNA
Chromosome
1q22
Autosomal Recessive
CMT2B1 is caused by autosomal recessive mutations in the LMN . . .
Axonal
CMT2B3
Associated Gene
GDAP1
Chromosome
8q21.11
Autosomal Recessive
CMT2B3 is caused by autosomal recessive mutations in the GDA . . .
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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