You are not alone. Here is where to start: learn the basics, find a specialist or center that sees AApoAI amyloidosis, look for clinical trials, and connect with others living with it — all in one place.
Open the full AApoAI amyloidosis hub →AApoAI amyloidosis is a rare condition. Also known as Apolipoprotein A-I amyloidosis, Familial amyloid nephropathy due to apolipoprotein A-I variant, Familial renal amyloidosis due to apolipoprotein A-I variant, Hereditary amyloid nephropathy due to apolipoprotein A-I variant, Hereditary renal amyloidosis due to apolipoprotein A-I variant. Tomeko brings together the specialists, research, clinical trials, treatments and community for AApoAI amyloidosis so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:93560 · OMIM 105200 · ICD-10 E85.0 · GARD 0019224
Start by learning the basics from an authoritative source, find a specialist or center that sees AApoAI 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 AApoAI amyloidosis, filtered to your area.
Tomeko shows live, recruiting studies for AApoAI amyloidosis from ClinicalTrials.gov on the hub.