All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02905 PEOA-4 ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 4 (PEOA-4) 610131 - 0 0 POLG2 - -
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