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Summary Literature (0)
MIM:605637 - CONGENITAL MYOPATHY 6 WITH OPHTHALMOPLEGIA; CMYP6

Xenbase Genes: myh2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011577 - myopathy, proximal, and ophthalmoplegia
MONDO:0018206 - childhood-onset autosomal recessive myopathy with external ophthalmoplegia
MONDO:0019195 - hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome

Disease Ontology (DO):
DOID:0080719 - congenital myopathy 6
DOID:3429 - inclusion body myositis