Neuronopathy, distal hereditary motor, type 7A

Any neuronopathy, distal hereditary motor in which the cause of the disease is a mutation in the SLC5A7 gene.

Also known as: SLC5A7 neuronopathy, distal hereditary motor, neuronopathy, distal hereditary motor caused by mutation in SLC5A7, Dhmn7A, Dhmnvp, HMN 7A, HMN7A, Harper-Young myopathy, neuronopathy, distal hereditary motor, type VIIA

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