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
04570 COXPD25 oxidative phosphorylation deficiency?, combined, type 25 (COXPD-25) 616430 AR - - MARS2 - -
03025 SPAX3 ataxia, spastic, type 3, autosomal dominant (SPAX-3) 611390 AR - - MARS2 - -
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