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CMT

Type 1

Charcot Marie Tooth Disease

Type 1

This catalog of the Type 1 CMT subtypes represents the current publicly available information for the various subtypes of CMT1. This catalog is comprised of information from several publicly available reputable sources, and each listing includes links to those sources.

 

CMT Type 1 is a demyelinating peripheral polyneuropathy and is autosomal dominant in inheritance. The subtypes of CMT1 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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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-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

CMT1G

PMP2

CMT1G

Chromosome

8q21.13

Associated Gene

Autosomal Dominant

CMT1G is caused by mutations in the PMP2 gene. Not to be con . . .

Demyelinating

HNPP

PMP22 (Usually a Deletion)

HNPP

Chromosome

17p.12-p11.2

Associated Gene

Autosomal Dominant

HNPP is the acronym for Hereditary Neuropathy with liability . . .

Demyelinating

Anchor 1

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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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