All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02821 COXPD-1 combined oxidative phosphorylation deficiency, type 1 (COXPD-1) 609060 - 7 7 GFM1 - -
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