The Cryptid Sloth
Where CMT and Life Meet
The Cryptid Sloth
Where CMT and Life Meet
The Cryptid Sloth
Where CMT and Life Meet
CMT4Me Podcast: CMT Raw and Unfiltered
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CMT4Me Podcast: CMT Raw and Unfiltered
Listen Here
CMT2X
Associated Gene
SPG11
Chromosome
15q21.1
Autosomal Recessive
CMT2X is caused by autosomal recessive mutations in the SPG1 . . .
Axonal
CMT2Z
Associated Gene
MORC2
Chromosome
22q12.2
Autosomal Dominant
CMT2Z is caused by autosomal dominant mutations in the MORC2 . . .
Axonal
SORD1-CMT
Associated Gene
SORD1
Chromosome
15q21.1
Autosomal Recessive
SORD1-CMT is caused by autosomal recessive mutations in the . . .
Axonal
CMT2Y
Associated Gene
VCP
Chromosome
9p13.3
Autosomal Dominant
CMT2Y is caused by autosomal dominant mutations in the VCP g . . .
Axonal
DST-CMT
Associated Gene
DST
Chromosome
6p12.1
Autosomal Recessive
DST-CMT is caused by autosomal recessive mutations in the DS . . .
Axonal
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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