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Summary Literature (0)
MIM:616505 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY; HMSN6B

Xenbase Genes: slc25a46

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014671 - neuropathy, hereditary motor and sensory, type 6B
MONDO:0019551 - hereditary motor and sensory neuropathy type 6