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
00720 MTDPS2 mitochondrial DNA depletion syndrome, type 2 (MTDPS-2, myopathic type) 609560 AR - - TK2 - -
06296 PEOB3 ?Progressive external ophthalmoplegia with Mi DNA deletions, autosomal recessive 3 617069 AR - - TK2 - -
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