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
06291 COQ10D8 ?Coenzyme Q10 deficiency, primary, 8 616733 AR - - COQ7 - -
07243 HMNR9 neuronopathy, distal hereditary motor, autosomal recessive, type 9 620402 AR - - COQ7 - -
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