All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01568 - Steatocystoma multiplex 184500 AD - - KRT17 - -
05989 PC pachyonychia congenita - - 262 262 KRT17, KRT6A, KRT6B, KRT6C - -
01486 PC2 pachyonychia congenita, type 2 167210 AD - - KRT17 - -
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