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 AD 0 0 KRT14 - -
01310 - epidermolysis bullosa, simplex, simplex, Weber-Cockayne type 131800 AD 0 0 ITGB4, KRT14, KRT5 - -
01312 - Epidermolysis bullosa simplex, Koebner type 131900 AD 0 0 KRT14, 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 - -
01460 NFJS Naegeli-Franceschetti-Jadassohn syndrome 161000 AD 0 0 KRT14 - -
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