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
03841 PEOA-6 ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 6 (PEOA-6) 615156 - 0 0 DNA2 - -
04089 SCKL-8 Seckel syndrome, type 8 (SCKL-8) 615807 - 0 0 DNA2 - -
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