All diseases

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06496 COXPD44 Combined oxidative phosphorylation deficiency 44 618855 AR - - FASTKD2 - -
01740 MC4DN mitochondrial complex IV deficiency (MCDN4) - - 17 17 APOPT1, COA5, COX10, COX14, COX20, COX5A, COX6A2, COX6B1, FASTKD2, PET100, SCO1, SURF1, TACO1 - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.