You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Tyrosinemia type III, look for clinical trials, and connect with others living with it — all in one place.
Open the full Tyrosinemia type III hub →Tyrosinemia type III is a rare condition. Also known as Tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency, Tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency, Tyrosinemia due to HPD deficiency, Tyrosinemia type III. Tomeko brings together the specialists, research, clinical trials, treatments and community for Tyrosinemia type III so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:69723 · OMIM 276710 · ICD-10 E70.2 · GARD 0010332
Start by learning the basics from an authoritative source, find a specialist or center that sees Tyrosinemia type III, 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 III, filtered to your area.
Tomeko shows live, recruiting studies for Tyrosinemia type III from ClinicalTrials.gov on the hub.