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
02245 MCOPS1 microphthalmia, syndromic, type 1 (Lenz microphthalmia syndrome) 309800 XL 3 - NAA10 - -
02193 OGDNS;NATD Ogden syndrome (OGDNS, N-terminal acetyltransferase deficiency (NATD)) 300855 XLD;XLR 1 - NAA10 - -
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