All diseases

1 entry on 1 page. Showing entry 1.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00108 ICRD Infantile cerebellar-retinal degeneration, 614559 (3)??mitochondrial? 614559 0 0 ACO2 - -