All diseases

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

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 - -
03441 RP39 retinitis pigmentosa, type 39 (RP39) 613809 - 1 1 USH2A - -
05415 USH Usher syndrome (USH) - - 457 455 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
05414 USH2 Usher syndrome, type II (USH-2) - - 1682 1682 GPR98, USH2A - -
02116 USH2A Usher syndrome,, type 2A (USH2A) 276901 AR 202 39 PDZD7, USH2A - -
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.