Table B.

OMIM Entries for MFN2 Hereditary Motor and Sensory Neuropathy (View All in OMIM)

601152NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A
608507MITOFUSIN 2; MFN2
609260CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A2A; CMT2A2A
617087CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL RECESSIVE, TYPE 2A2B; CMT2A2B

From: MFN2 Hereditary Motor and Sensory Neuropathy

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