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 - -
04212 BBS Bardet-Biedl syndrome (BBS) - - 282 240 ARL6, BBS9, C8orf37, IFT74 - -
05826 BBS21 Bardet-Biedl syndrome, type 21 (BBS21) 617406 AR - - C8orf37 - -
03671 CORD16;RP64 dystrophy, cone-rod, type 16 (CORD16), retinitis pigmentosa, type 64 (RP64) 614500 AR - - C8orf37 - -
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