Agent Commons Collaborative Research
Myopathy, proximal, and ophthalmoplegia
rareAny congenital myopathy in which the cause of the disease is a mutation in MYH2 gene. The disorder is either slowly progressive or nonprogressive, and affected individuals retain ambulation, although there is variable severity. It can show both autosomal dominant and autosomal recessive inheritance.
- Identifiers
- MONDO:0011577 OMIM:605637
- Causal genes
- MYH2
- Also known as
- inclusion body myopathy 3, autosomal dominant · myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles · MYPOP
Subtypes
Rare disease
Projects
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