You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Tyrosinemia type II, look for clinical trials, and connect with others living with it — all in one place.
Open the full Tyrosinemia type II hub →Tyrosinemia type II is a rare condition. Also known as Keratosis palmoplantaris-corneal dystrophy syndrome, Oculocutaneous tyrosinemia, Richner-Hanhart syndrome, Tyrosinemia due to TAT deficiency, Tyrosinemia due to tyrosine aminotransferase deficiency, Tyrosinemia type II. Tomeko brings together the specialists, research, clinical trials, treatments and community for Tyrosinemia type II so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:28378 · OMIM 276600 · ICD-10 E70.2 · GARD 0003105
Start by learning the basics from an authoritative source, find a specialist or center that sees Tyrosinemia type II, 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 II, filtered to your area.
Tomeko shows live, recruiting studies for Tyrosinemia type II from ClinicalTrials.gov on the hub.