Miyoshi Myopathy Gene Set

Dataset DisGeNET 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 https://www.disgenet.org/browser/0/1/0/C1850808
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Genes

7 genes associated with the disease Miyoshi Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADD2 adducin 2 (beta)
ANO5 anoctamin 5
CAPN3 calpain 3, (p94)
DCTN1 dynactin 1
DYSF dysferlin
PARVB parvin, beta
PROM1 prominin 1