OnlineIMD
Mitochondrial Charcot-Marie-Tooth disease
Type
Phenotype
Associated genes
Gene list
MFN2
Mitofusin 2 deficiency
GDAP1
GDAP1 deficiency
MT-ATP6
Mitochondrial ATP synthase F0 subunit 6 deficiency
SURF1
SURF1 deficiency
SCO2
SCO2 deficiency
C12orf65
Parent entry
Mitochondrial peripheral neuropathy