You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive, look for clinical trials, and connect with others living with it — all in one place.
Open the full Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive hub →Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive is a rare condition. Also known as Autosomal recessive generalized EBS. Tomeko brings together the specialists, research, clinical trials, treatments and community for Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:89838 · OMIM 601001, 619599 · ICD-10 Q81.0 · GARD 0016778
Start by learning the basics from an authoritative source, find a specialist or center that sees Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive, 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 1D, generalized, intermediate or severe, autosomal recessive, filtered to your area.
Tomeko shows live, recruiting studies for Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive from ClinicalTrials.gov on the hub.