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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hereditary skeletal muscle disorder
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Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis
Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis 1
rare
Identifiers
MONDO:0859322
OMIM:620138
Causal genes
MLIP
Part of
Myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis
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