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MIM:616505 - NEUROPATHY, HEREDITARY MOTOR AND SENSORY, TYPE VIB, WITH OPTIC ATROPHY; HMSN6B
Xenbase Genes: slc25a46
Human Disease Resource: MIM
MONDO:0014671 - distal interphalangeal joint of manural digit 5 |
MONDO:0019551 - hereditary motor and sensory neuropathy type 6 |