All diseases

8 entries on 1 page. Showing entries 1 - 8.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05458 DFN deafness, nonsyndromic (DFN) - - 49 44 CDC14A, CDH23, CEACAM16, FAM65B, MYO15A, MYO6, MYO7A, OTOF, OTOG, PCDH15, PDZD7, TECTA, TMC1, USH1C - -
06877 DFNA deafness, nonsyndromic (DFNA, autosomal dominant) - - 20 8 GREB1L, MYO6, MYO7A, REST, TECTA, TMC1 - -
02352 DFNA11 deafness, autosomal dominant, type 11 (DFNA-11) 601317 AD 1 1 MYO7A - -
05400 DFNB deafness, autosomal recessive (DFNB) - - 955 951 CDH23, CIB2, FAM65B, GRXCR1, HGF, MYO15A, MYO7A, OTOF, OTOG, PCDH15, RDX, S1PR2, SERPINB6, STRC, TMC1, USH1C - autosomal recessive
02283 DFNB2 deafness, autosomal recessive, type 2 (DFNB-2) 600060 AR 7 7 MYO7A - -
05415 USH Usher syndrome (USH) - - 457 455 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
02115 USH1 Usher syndrome, type I (USH-1) - - 644 645 CDH23, MYO7A, PCDH15, USH1C, USH1G - -
05460 USH1B Usher syndrome, type Ib (USH-1B) 276900 AR 537 536 MYO7A - autosomal recessive
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