All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
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
02851 DFNB48 deafness, autosomal recessive, type 48 (DFNB48) 609439 AR 8 8 CIB2 - -
05415 USH Usher syndrome (USH) - - 457 455 ARSG, CDH23, CIB2, CLRN1, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A - -
03762 USH1J Usher syndrome, type 1J (USH1J) 614869 AR 1 1 CIB2 - -
Legend   How to query  


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