CMT4A
Associated Gene
GDAP1
Chromosme
8q21.11
Autosomal Recessive
CMT4A is caused by autosomal recessive mutations in the GDAP . . .
Demyelinating
CMT4B2
Associated Gene
SBF2
Chromosme
11p15.4
Autosomal Recessive
CMT4B2 is caused by autosomal recessive mutations in the SBF . . .
Demyelinating
CMT4C
Associated Gene
SH3TC2
Chromosme
5q32
Autosomal Recessive
CMT4C is caused by autosomal recessive mutations in the SH3T . . .
Demyelinating
CMT4B1
Associated Gene
MTMR2
Chromosme
11q21
Autosomal Recessive
CMT4B1 is caused by autosomal recessive mutations in the MTM . . .
Demylelinating
CMT4B3
Associated Gene
SBF1
Chromosme
22q13.33
Autosomal Recessive
CMT4B3 is caused by autosomal recessive mutations in the SBF . . .
Demyelinating
CMT4D
Associated Gene
NDRG1
Chromosme
8q24.22
Autosomal Recessive
CMT4D is caused by autosomal recessive mutations in the NDRG . . .
Demyelinating
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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