You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Methylmalonic aciduria and homocystinuria type cblF, look for clinical trials, and connect with others living with it — all in one place.
Open the full Methylmalonic aciduria and homocystinuria type cblF hub →Methylmalonic aciduria and homocystinuria type cblF is a rare condition. Also known as CblF defect, Cobalamin F defect, Combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF, Lysosomal membrane cobalamin transporter deficiency, Methylmalonic aciduria with homocystinuria, type cblF. Tomeko brings together the specialists, research, clinical trials, treatments and community for Methylmalonic aciduria and homocystinuria type cblF so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:79284 · OMIM 277380 · ICD-10 E72.1 · GARD 0003584
Start by learning the basics from an authoritative source, find a specialist or center that sees Methylmalonic aciduria and homocystinuria type cblF, 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 cblF, filtered to your area.
Tomeko shows live, recruiting studies for Methylmalonic aciduria and homocystinuria type cblF from ClinicalTrials.gov on the hub.