All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02969 COXPD4 combined oxidative phosphorylation deficiency, type 4 (COXPD-4) 610678 AR 1 1 TUFM - -
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