Neuronopathy, distal hereditary motor, type 2D

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the FBXO38 gene.

Also known as: FBXO38 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in FBXO38, HMN 2D, HMN2D, neuronopathy, distal hereditary motor, type IID, neuropathy, distal hereditary motor, type 2D, spinal muscular atrophy, distal, autosomal dominant, calf-predominant

15 clinical trials for this condition and its sub-types.