You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Methylmalonic aciduria and homocystinuria type cblD, look for clinical trials, and connect with others living with it — all in one place.
Open the full Methylmalonic aciduria and homocystinuria type cblD hub →Methylmalonic aciduria and homocystinuria type cblD is a rare condition. Also known as CblD defect, Cobalamin D defect, Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD, Methylmalonic aciduria with homocystinuria, type cblD. Tomeko brings together the specialists, research, clinical trials, treatments and community for Methylmalonic aciduria and homocystinuria type cblD so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79283 · OMIM 277410 · ICD-10 E72.1 · GARD 0003582
Start by learning the basics from an authoritative source, find a specialist or center that sees Methylmalonic aciduria and homocystinuria type cblD, 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 aciduria and homocystinuria type cblD, filtered to your area.
Tomeko shows live, recruiting studies for Methylmalonic aciduria and homocystinuria type cblD from ClinicalTrials.gov on the hub.