You are not alone. Here is where to start: learn the basics, find a specialist or center that sees 3-hydroxyisobutyryl-CoA hydrolase deficiency, look for clinical trials, and connect with others living with it — all in one place.
Open the full 3-hydroxyisobutyryl-CoA hydrolase deficiency hub →3-hydroxyisobutyryl-CoA hydrolase deficiency is a rare condition. Also known as HIBCH deficiency, Methacrylic aciduria, Valine metabolic defect. Tomeko brings together the specialists, research, clinical trials, treatments and community for 3-hydroxyisobutyryl-CoA hydrolase deficiency so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:88639 · OMIM 250620 · ICD-10 E71.1 · GARD 0013202
Start by learning the basics from an authoritative source, find a specialist or center that sees 3-hydroxyisobutyryl-CoA hydrolase 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 3-hydroxyisobutyryl-CoA hydrolase deficiency, filtered to your area.
Tomeko shows live, recruiting studies for 3-hydroxyisobutyryl-CoA hydrolase deficiency from ClinicalTrials.gov on the hub.