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MIM:605637 - MYOPATHY, PROXIMAL, AND OPHTHALMOPLEGIA
Echinobase Genes:
Human Disease Resource: MIM
DOID:0080719 - congenital myopathy 6 |
DOID:3429 - inclusion body myositis |
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DOID:0080719 - congenital myopathy 6 |
DOID:3429 - inclusion body myositis |