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Summary Literature (0)
MIM:618511 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIC, WITH OPTIC ATROPHY; HMSN6C

Xenbase Genes:

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0032792 - neuropathy, hereditary motor and sensory, type VIc, with optic atrophy