All diseases

5 entries on 1 page. Showing entries 1 - 5.
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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 - -
05949 DFNB57 deafness, autosomal recessive, type 57 (DFNB57) 618003 AR - - PDZD7 - -
05086 HL hearing loss (HL) - - 1295 1182 C10orf90, FAM179A, GRAP, MPZL2, PDZD7, PKHD1L1, USP48 - -
02116 USH2A Usher syndrome,, type 2A (USH2A) 276901 AR 202 39 PDZD7, USH2A - -
00669 USH2C Usher syndrome,, type IIC (USH2C, GPR98/PDZD7 digenic) 605472 AR;DD 3 2 GPR98, PDZD7 - -
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