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
00895 RP61 retinitis pigmentosa, type 61 (RP61) 614180 - - - CLRN1 - -
05415 USH Usher syndrome (USH) - - 457 455 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
05459 USH3 Usher syndrome, type III (USH-3) - - 170 170 CLRN1, HARS - -
00894 USH3A Usher syndrome, type 3A (USH-3A) 276902 AR 3 3 CLRN1 - -
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