Details of Disease
General Information of Disease (ID: DISXRJUG)
Disease Name | Myopathy caused by variation in FKTN | ||||
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Synonyms | FKTN-related myopathy; FKTN myopathy; myopathy caused by mutation in FKTN | ||||
Definition | Any myopathy in which the cause of the disease is a variation in the FKTN gene. | ||||
Disease Hierarchy | |||||
Molecular Interaction Atlas (MIA) of This Disease
Molecular Interaction Atlas (MIA) | |||||||||||||||||||||||||
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This Disease Is Related to 1 DOT Molecule(s)
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References