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
03226 FNEPPK1 keratoderma, palmoplantar, nonepidermolytic, focal, type 1 (FNEPPK-1) 613000 AD 0 0 KRT16 - -
01485 PC1 pachyonychia congenita, type 1 167200 AD 0 0 KRT16 - -
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