Miyoshi myopathy Gene Set

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
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Genes

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