G2Cdb::Human Disease report
- Disease id
- D00000256
- Name
- Scapulo-peroneal myopathy
- Nervous system disease
- no
Genes (1)
| Gene | Name/Description | Mutations Found | Literature | Mutations Type | Genetic association? |
|---|---|---|---|---|---|
| G00002430 | MYH6 myosin, heavy chain 6, cardiac muscle, alpha |
Y | (17336526) | Single nucleotide polymorphism (SNP) | Y |