All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04014 COXPD-18 combined oxidative phosphorylation deficiency, type 18 (COXPD-18) 615578 - 0 0 SFXN4 - -
04242 FRDA Friedreich ataxia (FRDA) - - 11 11 FXN - -
01793 FRDA-1 Friedreich ataxia, type 1 (FRDA-1) 229300 - 0 0 FXN - -
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