You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Ornithine aminotransferase deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full Ornithine aminotransferase deficiency hub →Ornithine aminotransferase deficiency is a rare condition. Also known as HOGA, Hyperornithinemia, Hyperornithinemia-gyrate atrophy of choroid and retina syndrome, Ornithine aminotransferase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Ornithine aminotransferase deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:414 · OMIM 258870 · ICD-10 E72.4 · GARD 0006556
Start by learning the basics from an authoritative source, find a specialist or center that sees Ornithine aminotransferase deficiency, 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 Ornithine aminotransferase deficiency, filtered to your area.
Tomeko shows live, recruiting studies for Ornithine aminotransferase deficiency from ClinicalTrials.gov on the hub.