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
02499 - Febrile seizures, familial, 4 604352 - 0 0 GPR98 - -
05415 USH Usher syndrome (USH) - - 290 289 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
05414 USH-2 Usher syndrome, type II (USH-2) - - 1668 1668 GPR98, USH2A - -
00669 USH2C syndrome, Usher, type IIC (USH2C, GPR98/PDZD7 digenic) 605472 AR;DD 1 1 GPR98, PDZD7 - -
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