CMTDIA

CMTDIA

Associated Gene

Gene Unknown

Chromosome

10q24.1-q25.1

Autosomal Dominant

The underlying genetic cause for Dominant Intermediate CMT-A . . .

Intermediate

CMTDIC

CMTDIC

Associated Gene

YARS1

Chromosome

1p35.1

Autosomal Dominant

Dominant Intermediate CMT-C is caused by autosomal dominant . . .

Intermediate

CMTDIE

CMTDIE

Associated Gene

INF2

Chromosome

14q32.33

Autosomal Dominant

Dominant Intermediate CMT-E is caused by autosomal dominant . . .

Intermediate

CMTDIG

CMTDIG

Associated Gene

NEFL

Chromosome

8p21.2

Autosomal Dominant

Dominant Intermediate CMT-G is caused by autosomal dominant . . .

Intermediate

CMTDIB

CMTDIB

Associated Gene

DNM2

Chromosome

19p13.2

Autosomal Dominant

Dominant Intermediate CMT-B is caused by autosomal dominant . . .

Intermediate

CMTDID

CMTDID

Associated Gene

MPZ

Chromosome

1q23.3

Autosomal Dominant

Dominant Intermediate CMT-D is caused by autosomal dominant . . .

Intermediate

CMTDIF

CMTDIF

Associated Gene

GNB4

Chromosome

3q26.33

Autosomal Dominant

Dominant Intermediate CMT-F is caused by autosomal dominant . . .

Intermediate

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CMT

Dominant Intermediate

Charcot Marie Tooth Disease

Dominant Intermediate

(CMT-DI)

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

 

Dominant Intermediate CMT is a type of CMT in which the nerve conduction characteristics overlap that which is seen in demyelinating CMT and that which is seen in axonal CMT. Dominant Intermediate CMT isn’t necessarily a demyelinating CMT nor an axonal CMT, it is somewhere in between—it is intermediate. CMT-DI is autosomal dominant in inheritance. The subtypes of CMT-DI each fit these descriptions.

 

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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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-RI

Recessive

Intermediate

Intermediate
and
Autosomal Recessive
In Inheritance

The Cryptid Sloth

Where CMT and Life Meet