All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01282 - Dermatopathia pigmentosa reticularis 125595 0 0 KRT14 - -
01309 - Epidermolysis bullosa herpetiformis, Dowling-Meara 131760 0 0 KRT14, KRT5 - -
01310 - epidermolysis bullosa, simplex, simplex, Weber-Cockayne type 131800 0 0 ITGB4, KRT14, KRT5 - -
01312 - Epidermolysis bullosa simplex, Koebner type 131900 0 0 KRT14, KRT5 - -
02335 EBSB-1 epidermolysis bullosa simplex, autosomal recessive, type 1 (EBSB-1) 601001 0 0 KRT14, KRT5 - -
01460 Naegeli Naegeli syndrome 161000 0 0 KRT14 - -