You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Methylmalonic acidemia with homocystinuria, type cblX, look for clinical trials, and connect with others living with it — all in one place.
Open the full Methylmalonic acidemia with homocystinuria, type cblX hub →Methylmalonic acidemia with homocystinuria, type cblX is a rare condition. Also known as Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX, Methylmalonic aciduria with homocystinuria, type cblX. Tomeko brings together the specialists, research, clinical trials, treatments and community for Methylmalonic acidemia with homocystinuria, type cblX so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:369962 · OMIM 309541 · ICD-10 E71.1 · GARD 0013137
Start by learning the basics from an authoritative source, find a specialist or center that sees Methylmalonic acidemia with homocystinuria, type cblX, 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 cblX, filtered to your area.
Tomeko shows live, recruiting studies for Methylmalonic acidemia with homocystinuria, type cblX from ClinicalTrials.gov on the hub.