You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Hawkinsinuria, look for clinical trials, and connect with others living with it — all in one place.
Open the full Hawkinsinuria hub →Hawkinsinuria is a rare condition. Also known as 4-HPPD deficiency, 4-alpha-hydroxyphenylpyruvate hydroxylase deficiency, 4-hydroxyphenylpyruvic acid dioxygenase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Hawkinsinuria so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:2118 · OMIM 140350 · ICD-10 E70.2 · GARD 0005668
Start by learning the basics from an authoritative source, find a specialist or center that sees Hawkinsinuria, 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 Hawkinsinuria, filtered to your area.
Tomeko shows live, recruiting studies for Hawkinsinuria from ClinicalTrials.gov on the hub.