All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02953 COXPD-3 combined oxidative phosphorylation deficiency, type 3 (COXPD-3) 610505 - 1 1 TSFM - -
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