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CMT4E

CMT4E

Associated Gene

EGR2

Chromosme

10q21.3

Autosomal Recessive

CMT4E is caused by autosomal recessive mutations in the EGR2 . . .

Demyelinating

CMT4G

CMT4G

Associated Gene

HK1

Chromosme

10q22.1

Autosomal Recessive

CMT4G is caused by autosomal recessive mutations in the HK1 . . .

Demyelinating

CMT4J

CMT4J

Associated Gene

FIG4

Chromosme

6q21

Autosomal Recessive

CMT4J is caused by autosomal recessive mutations in the FIG4 . . .

Demyelinating

CMT4F

CMT4F

Associated Gene

PRX

Chromosme

19q13.2

Autosomal Recessive

CMT4F is caused by autosomal recessive mutations in the PRX . . .

Demyelinating

CMT4H

CMT4H

Associated Gene

FGD4

Chromosme

12p11.21

Autosomal Recessive

CMT4H is caused by autosomal recessive mutations in the FGD4 . . .

Demyelinating

CMT4K

CMT4K

Associated Gene

SURF1

Chromosme

9q34.2

Autosomal Recessive

CMT4K is caused by autosomal recessive mutations in the SURF . . .

Demyelinating

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CMT

Type 4

Charcot Marie Tooth Disease

Type 4

This catalog of the Type 4 CMT subtypes represents the current publicly available information for the various subtypes of CMT4. This catalog is comprised of information from several publicly available reputable sources, and each listing includes links to those sources.

 

CMT Type 4 is a demyelinating peripheral polyneuropathy and is autosomal recessive in inheritance. The subtypes of CMT4 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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CMT2

CMT

Type 2

Axonal
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

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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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