
CMT4E
Associated Gene
EGR2
Chromosme
10q21.3
Autosomal Recessive
CMT4E is caused by autosomal recessive mutations in the EGR2 . . .
Demyelinating

CMT4G
Associated Gene
HK1
Chromosme
10q22.1
Autosomal Recessive
CMT4G is caused by autosomal recessive mutations in the HK1 . . .
Demyelinating

CMT4J
Associated Gene
FIG4
Chromosme
6q21
Autosomal Recessive
CMT4J is caused by autosomal recessive mutations in the FIG4 . . .
Demyelinating

CMT4F
Associated Gene
PRX
Chromosme
19q13.2
Autosomal Recessive
CMT4F is caused by autosomal recessive mutations in the PRX . . .
Demyelinating

CMT4H
Associated Gene
FGD4
Chromosme
12p11.21
Autosomal Recessive
CMT4H is caused by autosomal recessive mutations in the FGD4 . . .
Demyelinating

CMT4K
Associated Gene
SURF1
Chromosme
9q34.2
Autosomal Recessive
CMT4K is caused by autosomal recessive mutations in the SURF . . .
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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