You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Tyrosinemia type I, look for clinical trials, and connect with others living with it — all in one place.
Open the full Tyrosinemia type I hub →Tyrosinemia type I is a rare condition. Also known as FAH deficiency, Fumarylacetoacetase deficiency, Fumarylacetoacetate hydrolase deficiency, Hepatorenal tyrosinemia, Tyrosinemia type I. Tomeko brings together the specialists, research, clinical trials, treatments and community for Tyrosinemia type I so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:882 · OMIM 276700 · ICD-10 E70.2 · GARD 0002658
Start by learning the basics from an authoritative source, find a specialist or center that sees Tyrosinemia type I, 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 Tyrosinemia type I, filtered to your area.
Tomeko shows live, recruiting studies for Tyrosinemia type I from ClinicalTrials.gov on the hub.