All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00040 NSHL non-syndromic hearing loss - - 8 1 GJB2, GJB6 - -
00108 PDS Pendred syndrome 274600 AR 2 2 DUOX2, GJB2, SCARB2, SLC26A4 ears -
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