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
04199 COQ10D coenzyme Q10 deficiency (COQ10D) - - 47 47 COQ4, COQ5, PDSS1 - -
04428 COQ10D7 coenzyme Q10 deficiency, primary, type 7 (COQ10D-7) 616276 AR - - COQ4 - -
07231 SPAX10 ataxia, spastic, type 10 620666 AR - - COQ4 - -
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