| Human Disease |
Term: Neuronopathy, Distal Hereditary Motor, Type Viia; HMN7A
OMIM ID: 158580
|
| Synonyms |
Dhmn7a; DHMNVP; Harper-Young Myopathy; Hmn Viia; Neuropathy, Distal Hereditary Motor, Type Viia; Spinal Muscular Atrophy, Distal, with Vocal Cord Paralysis |
| Associated Genes |
Orthologous mouse and human markers where mutations in one or both species have been associated with phenotypes characteristic of this disease.
Mouse Gene |
Human Gene |
|
Characteristics of this human disease are associated with mutations in... |
| |
|
|
|
|
 ...the human gene.
MGI data currently do not associate this disease with mutations in the orthologous mouse gene. |
| |
|
|
|
Analysis Tools