Oculocraniosomatic myopathy (Q103475): Difference between revisions

Revision as of 09:14, 17 August 2026

Mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis.

Language	Label	Description	Also known as
default for all languages	ID_121795048
English	Oculocraniosomatic myopathy	Mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis.

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CID11:ID_121795048

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dki-india-ID_121795048

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Concluído

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