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
05458 DFN deafness, nonsyndromic (DFN) - - 50 45 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 - -
02596 DFNA36 deafness, autosomal dominant, type 36 (DFNA-36) 606705 AD - - TMC1 - -
05400 DFNB deafness, autosomal recessive (DFNB) - - 977 973 CDH23, CIB2, FAM65B, GIPC3, GRXCR1, HGF, MYO15A, MYO7A, OTOF, OTOG, PCDH15, RDX, S1PR2, SERPINB6, STRC, TMC1, USH1C - autosomal recessive
02330 DFNB7 deafness, autosomal recessive, type 7 (DFNB-7) 600974 AR 10 10 TMC1 - -
Legend   How to query  


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