CMT2A

CMT2A

Associated Gene

MFN2

Chromosome

1p36.22

Autosomal Dominant

CMT2A is caused by autosomal dominant mutations in the MFN2 . . .

Axonal

CMT2B

CMT2B

Associated Gene

RAB7

Chromosome

3q21.3

Autosomal Dominant

CMT2B is caused by autosomal dominant mutations in the RAB7 . . .

Axonal

CMT2B2

CMT2B2

Associated Gene

MED25

Chromosome

19q13.33

Autosomal Recessive

CMT2B2 is caused by autosomal recessive mutations in the MED . . .

Axonal

CMT2A2B

CMT2A2B

Associated Gene

MFN2

Chromosome

1p36.22

Autosomal Recessive

CMT2A2B is caused by autosomal recessive mutations in the MF . . .

Axonal

CMT2B1

CMT2B1

Associated Gene

LMNA

Chromosome

1q22

Autosomal Recessive

CMT2B1 is caused by autosomal recessive mutations in the LMN . . .

Axonal

CMT2B3

CMT2B3

Associated Gene

GDAP1

Chromosome

8q21.11

Autosomal Recessive

CMT2B3 is caused by autosomal recessive mutations in the GDA . . .

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