All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05439 COXPD32 combined oxidative phosphorylation deficiency, type 1 (COXPD-32) 617664 AR - - MRPS34 - autosomal recessive
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