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
04014 COXPD18 combined oxidative phosphorylation deficiency, type 18 (COXPD-18) 615578 AR - - SFXN4 - -
04242 FRDA Friedreich ataxia (FRDA) 229300 AR 18 17 FXN - -
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