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
01151 COXPD15 combined oxidative phosphorylation deficiency, type 15 (COXPD-15) 614947 AR - - MTFMT - -
06275 MC1DN27 Mi complex I deficiency, nuclear type 27 618248 AR - - MTFMT - -
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