OPHTHALMOPLEGIC NEUROMUSCULAR DISORDER WITH ABNORMAL MITOCHONDRIA
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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7
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OrphanetNr:
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OMIM Id:
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258470
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ICD-10:
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Age of onset:
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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No data available.
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1
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(HPO:0000508)
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Ptosis |
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459 / 7739
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2
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(HPO:0000602)
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Ophthalmoplegia |
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56 / 7739
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3
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(HPO:0001291)
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Abnormality of the cranial nerves |
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27 / 7739
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4
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(HPO:0008316)
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Abnormal mitochondria in muscle tissue |
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5 / 7739
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5
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(HPO:0001324)
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Muscle weakness |
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859 / 7739
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6
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(OMIM)
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Abnormal mitochondria on muscle biopsy |
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1 / 7739
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7
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(OMIM)
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Diffuse, low-density deep cerebral white material on CT |
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1 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |