You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Familial anetoderma, look for clinical trials, and connect with others living with it — all in one place.
Open the full Familial anetoderma hub →Familial anetoderma is a rare condition. Also known as Hereditary anetoderma, Hereditary macular atrophy. Tomeko brings together the specialists, research, clinical trials, treatments and community for Familial anetoderma so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:228277 · ICD-10 L90.8 · GARD 0020585
Start by learning the basics from an authoritative source, find a specialist or center that sees Familial anetoderma, 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 Familial anetoderma, filtered to your area.
Tomeko shows live, recruiting studies for Familial anetoderma from ClinicalTrials.gov on the hub.