All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06877 DFNA deafness, nonsyndromic (DFNA, autosomal dominant) - - 20 8 GREB1L, MYO6, MYO7A, REST, TECTA, TMC1 - -
06991 DFNA80 deafness, autosomal dominant, type 80 619274 AD - - GREB1L - -
05805 RHDA hypodysplasia/aplasia, renal (RHDA) - - 1 1 GREB1L - -
05806 RHDA3 hypodysplasia/aplasia, renal, type 3 (RHDA-3 617805 AD - - GREB1L - -
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