All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00658 MTDPS8A mitochondrial DNA depletion syndrome, type 8A (MTDPS8A, encephalomyopathic type with renal tubulopathy) 612075 AR - - RRM2B - -
00659 PEOA5 ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 5 (PEOA-5) 613077 AD - - RRM2B - -
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