All diseases

OMIM ID
601152
OMIM term:
HEREDITARY MOTOR AND SENSORY NEUROPATHY VI
Alternative terms:
HMSN6
HMSN VI
PERIPHERAL NEUROPATHY AND OPTIC ATROPHY
CHARCOT-MARIE-TOOTH DISEASE, TYPE 6; CMT6
(∗) Location:
1p36.22  
(†) Associated OMIM genes:
MFN2  
(‡) Associated MGI genes:

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