All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
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 - -
01314 - Epidermolysis bullosa simplex with mottled pigmentation 131960 - - - KRT5 - -
01540 - Reticulate acropigmentation of Kitamura 179850 - - - KRT5 - -
02335 - Epidermolysis bullosa simplex, autosomal recessive 601001 - - - KRT14, KRT5 - -
02848 - Epidermolysis bullosa simplex with migratory circinate erythema 609352 - - - KRT5 - -
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