All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04214 - retinal disease - - 48173 45676 ADAM9, AGBL5, ARL2BP, BBS2, C8orf37, IFT43, KIF3B, MERTK, PDE6G, REEP6, SCAPER, USH2A, ZNF408 - -
00058 CORD dystrophy, cone-rod (CORD) - - 363 361 ADAM9, DRAM2, GUCY2D, PITPNM3, POC1B, RAB28, TTLL5 - -
03188 CORD9 dystrophy, cone-rod, type 9 (CORD-9) 612775 AR - - ADAM9 - -
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