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Summary Literature (0)
MIM:601152 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIA, WITH OPTIC ATROPHY; HMSN6A

Xenbase Genes: mfn2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011002 - neuropathy, hereditary motor and sensory, type 6A

Disease Ontology (DO):
DOID:0080068 - Charcot-Marie-Tooth disease type 6