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CMT2L

CMT2L

Associated Gene

HSPB8

Chromosome

12q24.23

Autosomal Dominant

CMT2L is caused by autosomal dominant mutations in the HSPB8 . . .

Axonal

CMT2N

CMT2N

Associated Gene

AARS1

Chromosome

16q22.1

Autosomal Dominant

CMT2N is caused by autosomal dominant mutations in the AARS1 . . .

Axonal

CMT2P

CMT2P

Associated Gene

LRSAM1

Chromosome

9q33.3-q34.1

Autosomal Dominant or Recessive

CMT2P is caused by autosomal dominant and autosomal recessiv . . .

Axonal

CMT2M

CMT2M

Associated Gene

DNM2

Chromosome

19p13.2

Autosomal Dominant

CMT2M is caused by autosomal dominant mutations in the DNM2 . . .

Axonal

CMT2O

CMT2O

Associated Gene

DYNC1H1

Chromosome

14q32.31

Autosomal Dominant

CMT2O is caused by autosomal dominant mutations in the DYNC1 . . .

Axonal

CMT2Q

CMT2Q

Associated Gene

DHTKD1

Chromosome

10p14

Autosomal Dominant

CMT2Q is caused by autosomal dominant mutations in the DHTKD . . .

Axonal

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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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CMT1

CMT

Type 1

Demyelinating
and
Autosomal Dominant
In Inheritance

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CMT4

CMT

Type 4

Demyelinating
and
Autosomal Recessive
In Inheritance

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CMTX

X-Linked

CMT

X-Linked Dominant
and
X-Linked Recessive
In Inheritance

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CMT-DI

Dominant

Intermediate

Intermediate
and
Autosomal Dominant
In Inheritance

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CMT-RI

Recessive

Intermediate

Intermediate
and
Autosomal Recessive
In Inheritance

The Cryptid Sloth

Where CMT and Life Meet

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All information published on this website is provided for informational and reference purposes only and should not be construed as medical advice or as a medical diagnosis. This website is not intended to replace or to substitute the opinion and advice of your physician. Always consult with your physician.

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