Disease

Epidermolysis Bullosa Simplex

3 associated genes · 0 supporting PMIDs
File:FootEBS.JPGWikimedia Commons

Epidermolysis bullosa simplex (EBS) is a disorder resulting from mutations in the genes encoding keratin 5 or keratin 14. It is one of the major forms of epidermolysis bullosa, a group of genetic conditions that cause the skin to be very fragile and to blister easily.

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3 entriesassociated with
GeneScorePMIDs
ITGB40.200
KRT50.230
KRT140.230