| http://dbpedia.org/ontology/abstract
|
Oculopharyngodistal myopathy is a rare genetic disorder characterized by progressive muscle weakness affecting various parts of the body.
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10872
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1124985533
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http://dbpedia.org/resource/RILPL1 +
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, http://dbpedia.org/resource/Medical_genetics +
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, http://dbpedia.org/resource/Ophthalmoparesis +
, http://dbpedia.org/resource/Chinese_people +
, http://dbpedia.org/resource/Japanese_people +
, http://dbpedia.org/resource/Myopathy +
, http://dbpedia.org/resource/Dysarthria +
, http://dbpedia.org/resource/Category:Genetic_diseases_and_disorders +
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, http://dbpedia.org/resource/Dysphagia +
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|
| http://dbpedia.org/property/causes
|
http://dbpedia.org/resource/Genetic_mutation +
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| http://dbpedia.org/property/deaths
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-
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| http://dbpedia.org/property/duration
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lifelong
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| http://dbpedia.org/property/frequency
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rare, approximately 78 families are known to carry the gene for this condition
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| http://dbpedia.org/property/onset
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adulthood
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| http://dbpedia.org/property/prevention
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none
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| http://dbpedia.org/property/risks
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being of East Asian descent
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| http://dbpedia.org/property/specialty
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http://dbpedia.org/resource/Medical_genetics +
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| http://dbpedia.org/property/symptoms
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widespread muscle weakness and atrophy alongside other symptoms such as tremors and gait instability
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| rdf:type |
http://dbpedia.org/ontology/Disease +
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|
| rdfs:comment |
Oculopharyngodistal myopathy is a rare genetic disorder characterized by progressive muscle weakness affecting various parts of the body.
|
| rdfs:label |
Oculopharyngodistal myopathy
|
