You are not alone. Here is where to start: learn the basics, find a specialist or center that sees HSD10 disease, infantile type, look for clinical trials, and connect with others living with it — all in one place.
Open the full HSD10 disease, infantile type hub →HSD10 disease, infantile type is a rare condition. Also known as 2-methyl-3-hydroxybutyric aciduria, classic type, 2-methyl-3-hydroxybutyric aciduria, infantile type, 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, classic type, 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, infantile type, HSD10 deficiency, classic type, HSD10 deficiency, infantile type, HSD10 disease, classic type, MHBD deficiency, classic type. Tomeko brings together the specialists, research, clinical trials, treatments and community for HSD10 disease, infantile type so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:391428 · OMIM 300438 · ICD-10 E72.8 · GARD 0017622
Start by learning the basics from an authoritative source, find a specialist or center that sees HSD10 disease, infantile type, 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 HSD10 disease, infantile type, filtered to your area.
Tomeko shows live, recruiting studies for HSD10 disease, infantile type from ClinicalTrials.gov on the hub.