All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04214 retinal disease retinal disease - - 22245 19940 ADAM9, AGBL5, ARL2BP, BBS2, C8orf37, IFT43, KIF3B, MERTK, PDE6G, REEP6, SCAPER, USH2A, ZNF408 - -
03441 RP39 retinitis pigmentosa, type 39 (RP39) 613809 - 1 1 USH2A - -
05415 USH Usher syndrome (USH) - - 265 264 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
05414 USH-2 Usher syndrome, type II (USH-2) - - 1668 1668 GPR98, USH2A - -
02116 USH2A syndrome, Usher, type 2A (USH2A) 276901 AR 17 16 PDZD7, USH2A - -
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