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
03950 COXPD17 combined oxidative phosphorylation deficiency, type 17 (COXPD-17) 615440 AR - - ELAC2 - -
03714 HPC2 cancer, prostate, hereditary, type 2 (HPC-12) 614731 - - - ELAC2 - -
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