You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Epidermolysis bullosa simplex, Ogna type, look for clinical trials, and connect with others living with it — all in one place.
Open the full Epidermolysis bullosa simplex, Ogna type hub →Epidermolysis bullosa simplex, Ogna type is a rare condition. Also known as PLEC-related intermediate EBS without extracutaneous involvement. Tomeko brings together the specialists, research, clinical trials, treatments and community for Epidermolysis bullosa simplex, Ogna type so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79401 · OMIM 131950 · ICD-10 Q81.0 · GARD 0002148
Start by learning the basics from an authoritative source, find a specialist or center that sees Epidermolysis bullosa simplex, Ogna type, and connect with a patient organization. Tomeko brings these together on one hub.
Use Tomeko's specialist and Centers-of-Excellence directories to find clinicians who treat Epidermolysis bullosa simplex, Ogna type, filtered to your area.
Tomeko shows live, recruiting studies for Epidermolysis bullosa simplex, Ogna type from ClinicalTrials.gov on the hub.