All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05458 DFN deafness, nonsyndromic (DFN) - - 46 43 CDH23, CEACAM16, FAM65B, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, PDZD7, TECTA, TMC1, USH1C - -
05400 DFNB deafness, autosomal recessive (DFNB) - - 870 869 CDH23, CIB2, FAM65B, MYO15A, MYO7A, OTOF, OTOG, PCDH15, S1PR2, STRC, TMC1, USH1C - autosomal recessive
02416 DFNB18A deafness, autosomal recessive, type 18A 602092 AR 1 2 USH1C - -
05415 USH Usher syndrome (USH) - - 472 471 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
02115 USH1 Usher syndrome, type I (USH-1) - - 643 644 CDH23, MYO7A, PCDH15, USH1C, USH1G - -
02117 USH1C Usher syndrome, type 1C (USH-1C) 276904 AR 0 0 USH1C - -
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