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Cap myopathy
- Other Names:
Cap disease; Congenital myopathy with capsCap disease; Congenital myopathy with caps
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Many rare diseases have limited information. Currently GARD is able to provide the following information for this disease:
30 Symptoms
Cap myopathy is a genetic disease, which means that it is caused by one or more genes not working correctly.
The following gene(s) are known to be associated with this disease: MYPN, TPM2, TPM3
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All individuals inherit two copies of most genes. The number of copies of a gene that need to have a disease-causing variant affects the way a disease is inherited. This disease is inherited in the following pattern(s):
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Last Updated: Nov. 8, 2021