You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Congenital hereditary endothelial dystrophy of cornea, look for clinical trials, and connect with others living with it — all in one place.
Open the full Congenital hereditary endothelial dystrophy of cornea hub →Congenital hereditary endothelial dystrophy of cornea is a rare condition. Also known as Autosomal recessive CHED, Autosomal recessive congenital hereditary endothelial dystrophy, CHED2, CHEDII, Congenital hereditary endothelial dystrophy type 2, Infantile hereditary endothelial dystrophy, Maumenee corneal dystrophy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Congenital hereditary endothelial dystrophy of cornea so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:293603 · OMIM 217700 · ICD-10 H18.5 · GARD 0006196
Start by learning the basics from an authoritative source, find a specialist or center that sees Congenital hereditary endothelial dystrophy of cornea, 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 Congenital hereditary endothelial dystrophy of cornea, filtered to your area.
Tomeko shows live, recruiting studies for Congenital hereditary endothelial dystrophy of cornea from ClinicalTrials.gov on the hub.