| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Miyoshi myopathy (MM) is a distal myopathy (see this term) characterized by weakness in the distal lower extremity posterior compartment (gastrocnemius and soleus muscles) and is associated with difficulties in standing on tip toes. (Orphanet Rare Disease Ontology, Orphanet_45448) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C537480 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Miyoshi myopathy from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| DYSF | dysferlin | 2.88009 |
