Oculocraniosomatic myopathy (Q103475): Difference between revisions
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Doença neuromuscular mitocondrial caracterizada por início antes dos 20 anos de idade, oftalmoplegia, ptose e retinite pigmentar. | |||
| description / en | description / en | ||
Mitochondrial neuromuscular disease characterised by an onset before the age of 20 years, ophthalmoplegia, ptosis and pigmentary retinitis. | |||
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. |
