You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency hub →Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency is a rare condition. Also known as Crotonase deficiency, ECHS1D. Tomeko brings together the specialists, research, clinical trials, treatments and community for Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:653880 · OMIM 616277 · ICD-10 E71.1 · GARD 0013019
Start by learning the basics from an authoritative source, find a specialist or center that sees Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency, and connect with a patient organization. Tomeko brings these together on one hub.
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Tomeko shows live, recruiting studies for Mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency from ClinicalTrials.gov on the hub.