All diseases

4 entries on 1 page. Showing entries 1 - 4.
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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 - -
05075 EVR6 vitreoretinopathy, exudative, type 6 (EVR-6) 616468 AD 6 - ZNF408 - -
04240 EVR;FEVR vitreoretinopathy, exudative (EVR; familial FVER)) - - 259 231 CTNNB1, FZD4, LRP5, NDP, TSPAN12, ZNF408 - -
05076 RP72 retinitis pigmentosa, type 72 (RP72) 616469 AR 8 - ZNF408 - -
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