| Disease ID | Source | Name | Description |
| 615575 | OMIM | Neuronopathy, distal hereditary motor, 2D (HMN2D) | A disorder characterized by onset of slowly progressive distal lower limb weakness and atrophy between the second and fourth decades of life. Weakness usually begins in the calf muscles and later involves more proximal muscles. The severity is variable, and some patients have difficulty walking or running. Most also have upper limb involvement, particularly of the triceps and intrinsic hand muscles. Some patients may lose independent ambulation later in the disease course. Sensory impairment is typically not present, and cognition and bulbar function are normal. The disease is caused by variants affecting the gene represented in this entry. |