Preferred Name | Ophthalmoplegia, Chronic Progressive External [Disease/Finding] | |
Synonyms |
Graefe Disease Graefe's Disease Ocular Myopathy of Von Graefe-Fuchs Ophthalmoplegia, Chronic Progressive External Mitochondrial Ocular Myopathy CPEO Chronic Progressive External Ophthalmoplegia Ophthalmoplegia, Progressive External Progressive External Ophthalmoplegia Ocular Muscular Dystrophy |
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ID |
http://purl.bioontology.org/ontology/NDFRT/N0000003562 |
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altLabel |
Graefe Disease Graefe's Disease Ocular Myopathy of Von Graefe-Fuchs Ophthalmoplegia, Chronic Progressive External Mitochondrial Ocular Myopathy CPEO Chronic Progressive External Ophthalmoplegia Ophthalmoplegia, Progressive External Progressive External Ophthalmoplegia Ocular Muscular Dystrophy |
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cui |
C0162674 |
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MESH DEFINITION |
A mitochondrial myopathy characterized by slowly progressive paralysis of the levator palpebrae, orbicularis oculi, and extraocular muscles. Ragged-red fibers and atrophy are found on muscle biopsy. Familial and sporadic forms may occur. Disease onset is usually in the first or second decade of life, and the illness slowly progresses until usually all ocular motility is lost. (From Adams et al., Principles of Neurology, 6th ed, p1422) |
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MESH DUI |
D017246 |
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MeSH name |
Ophthalmoplegia, Chronic Progressive External |
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MESH UI |
M0026169 |
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NDFRT kind |
DISEASE_KIND |
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notation |
N0000003562 |
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NUI |
N0000003562 |
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prefLabel |
Ophthalmoplegia, Chronic Progressive External [Disease/Finding] |
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SNOMED CID |
46252003 |
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tui |
T047 |
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subClassOf |