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CMT2E

CMT2E

Associated Gene

NEFL

Chromosome

8p21.2

Autosomal Dominant

CMT2E is caused by autosomal dominant mutations in the NEFL . . .

Axonal

CMT2F

CMT2F

Associated Gene

HSPB1

Chromosome

7q11.23

Autosomal Dominant

CMT2F is caused by autosomal dominant mutations in the HSPB1 . . .

Axonal

CMT2J

CMT2J

Associated Gene

MPZ

Chromosome

1q23.3

Autosomal Dominant

CMT2J is caused by autosomal dominant mutations in the MPZ g . . .

Axonal

CMT2EE

CMT2EE

Associated Gene

MPV17

Chromosome

2p23.3

Autosomal Recessive

CMT2EE is caused by autosomal recessive mutations in the MPV . . .

Axonal

CMT2I

CMT2I

Associated Gene

MPZ

Chromosome

1q23.3

Autosomal Dominant

CMT2I is caused by autosomal dominant mutations in the MPZ g . . .

Axonal

CMT2K

CMT2K

Associated Gene

GDAP1

Chromosome

8q21.11

Autosomal Dominant or Recessive

CMT2K is caused by autosomal dominant and autosomal recessiv . . .

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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