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
03573 LCA16 Leber congenital amaurosis, type 16 (LCA-16) 614186 AR - - KCNJ13 - -
01601 SVD vitreoretinal degeneration, snwoflake type (SVD) 193230 AD 1 1 KCNJ13 - -
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