Cure My Disease

Don't miss your cure!

Home News Browse Soon ready About
Log in / Sign up

Browse

Explore conditions, clinical trials, and the organisations running them.

Conditions By category Trials Sponsors

← All categories

Up to: Inherited epidermolysis bullosa

Epidermolysis bullosa dystrophica

A genetic skin disorder caused by mutations in the type VII collagen gene (COL7A1). It is characterized by the formation of blisters and scarring in the skin and mucous membranes.

23 trials tagged with this condition →

  • Recessive dystrophic epidermolysis bullosa 21 trials Sub-types →
  • Generalized dominant dystrophic epidermolysis bullosa 1 trial
  • Acral dystrophic epidermolysis bullosa 0 trials
  • Centripetalis recessive dystrophic epidermolysis bullosa 0 trials
  • Dystrophic epidermolysis bullosa pruriginosa 0 trials
  • Dystrophic epidermolysis bullosa, nails only 0 trials
  • Epidermolysis bullosa dystrophica Neurotrophica 0 trials
  • Epidermolysis bullosa dystrophica with subcorneal cleavage 0 trials
  • Localized dystrophic epidermolysis bullosa 0 trials
  • Pretibial dystrophic epidermolysis bullosa 0 trials
  • Recessive dystrophic epidermolysis bullosa-generalized other 0 trials
  • Transient bullous dermolysis of the newborn 0 trials

Cure My Disease

Helping patients find clinical trials that match their disease.

Why was Cure my disease built?

Explore

Home News Browse Glossary About Terms of use Contact us

This is a site from Cyber and Space