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
01310 - epidermolysis bullosa, simplex, simplex, Weber-Cockayne type 131800 AD - - ITGB4, KRT14, KRT5 - -
01312 - Epidermolysis bullosa simplex, Koebner type 131900 AD - - KRT14, KRT5 - -
02848 - Epidermolysis bullosa simplex with migratory circinate erythema 609352 - - - KRT5 - -
01540 DDD1 Dowling-Degos disease 1 179850 AD - - KRT5 - -
02335 EBSB1 epidermolysis bullosa simplex, autosomal recessive, type 1 (EBSB-1) 601001 AR 3 3 KRT14, KRT5 - -
01309 EBSDM Epidermolysis bullosa herpetiformis, Dowling-Meara 131760 AD 1 1 KRT14, KRT5 - -
01314 EBSMP Epidermolysis bullosa simplex with mottled pigmentation 131960 AD - - KRT5 - -
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