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
00535 617070 Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4, 617070 (3) 617070 0 0 DGUOK - -
00031 MTDPS3 Mitochondrial DNA depletion syndrome 3 (hepatocerebral type), 251880 (3) 251880 0 0 C10orf2, DGUOK - -