You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Methylmalonic acidemia with homocystinuria, type cblJ, look for clinical trials, and connect with others living with it — all in one place.
Open the full Methylmalonic acidemia with homocystinuria, type cblJ hub →Methylmalonic acidemia with homocystinuria, type cblJ is a rare condition. Also known as CblJ defects, Cobalamin J defect, Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblJ, Methylmalonic aciduria with homocystinuria, type cblJ. Tomeko brings together the specialists, research, clinical trials, treatments and community for Methylmalonic acidemia with homocystinuria, type cblJ so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:369955 · OMIM 614857 · ICD-10 E71.1 · GARD 0012621
Start by learning the basics from an authoritative source, find a specialist or center that sees Methylmalonic acidemia with homocystinuria, type cblJ, 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 Methylmalonic acidemia with homocystinuria, type cblJ, filtered to your area.
Tomeko shows live, recruiting studies for Methylmalonic acidemia with homocystinuria, type cblJ from ClinicalTrials.gov on the hub.