You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Alkaptonuria, look for clinical trials, and connect with others living with it — all in one place.
Open the full Alkaptonuria hub →Alkaptonuria is a rare condition. Also known as Hereditary ochronosis, Homogentisic acid oxidase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Alkaptonuria so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:56 · OMIM 203500 · ICD-10 E70.2 · GARD 0005775
Start by learning the basics from an authoritative source, find a specialist or center that sees Alkaptonuria, 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 Alkaptonuria, filtered to your area.
Tomeko shows live, recruiting studies for Alkaptonuria from ClinicalTrials.gov on the hub.