All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01282 - Dermatopathia pigmentosa reticularis 125595 - - - KRT14 - -
01309 - Epidermolysis bullosa herpetiformis, Dowling-Meara 131760 - - - KRT14, KRT5 - -
01310 - Epidermolysis bullosa simplex, Cockayne-Touraine type 131800 - - - ITGB4, KRT14, KRT5 - -
01312 - Epidermolysis bullosa simplex, Koebner type 131900 - - - KRT14, KRT5 - -
02335 - Epidermolysis bullosa simplex, autosomal recessive 601001 - - - KRT14, KRT5 - -
01460 Naegeli Naegeli syndrome 161000 - - - KRT14 - -
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