Neuronopathy, distal hereditary motor, type 5C

MONDO:0030860

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the BSCL2 gene.

Also known as: DHMN5C, HMN5C, neuropathy, distal hereditary motor, type VC, spinal muscular atrophy, distal, type 5C

15 clinical trials for this condition and its sub-types, 0 tagged with Neuronopathy, distal hereditary motor, type 5C itself.

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