You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Succinyl-CoA acetoacetate transferase deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full Succinyl-CoA acetoacetate transferase deficiency hub →Succinyl-CoA acetoacetate transferase deficiency is a rare condition. Also known as OXCT1 deficiency, SCOT deficiency, Succinyl-CoA acetoacetate transferase deficiency, Succinyl-CoA:3-ketoacid CoA transferase deficiency. Tomeko brings together the specialists, research, clinical trials, treatments and community for Succinyl-CoA acetoacetate transferase deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:832 · OMIM 245050 · ICD-10 E71.3 · GARD 0004774
Start by learning the basics from an authoritative source, find a specialist or center that sees Succinyl-CoA acetoacetate transferase 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 Succinyl-CoA acetoacetate transferase deficiency, filtered to your area.
Tomeko shows live, recruiting studies for Succinyl-CoA acetoacetate transferase deficiency from ClinicalTrials.gov on the hub.