All diseases

2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03950 COXPD-17 combined oxidative phosphorylation deficiency, type 17 (COXPD-17) 615440 0 0 ELAC2 - -
03714 HPC-2 cancer, prostate, hereditary, type 2 (HPC-12) 614731 0 0 ELAC2 - -