You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Finnish type amyloidosis, look for clinical trials, and connect with others living with it — all in one place.
Open the full Finnish type amyloidosis hub →Finnish type amyloidosis is a rare condition. Also known as Familial amyloid polyneuropathy type IV, Familial amyloidosis, Finnish type, Gelsolin amyloidosis, Hereditary amyloidosis, Finnish type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Finnish type amyloidosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:85448 · OMIM 105120 · ICD-10 E85.1 · GARD 0002339
Start by learning the basics from an authoritative source, find a specialist or center that sees Finnish type amyloidosis, 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 Finnish type amyloidosis, filtered to your area.
Tomeko shows live, recruiting studies for Finnish type amyloidosis from ClinicalTrials.gov on the hub.