You are not alone. Here is where to start: learn the basics, find a specialist or center that sees Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type, look for clinical trials, and connect with others living with it — all in one place.
Open the full Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type hub →Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type is a rare condition. Also known as Glutaric aciduria type 2, severe neonatal type, MAD deficiency, severe neonatal type, MADD, severe neonatal type. Tomeko brings together the specialists, research, clinical trials, treatments and community for Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type so you can go from overwhelmed to oriented. For authoritative medical detail, see the reference sources below.
Identifiers: ORPHA:394529 · OMIM 231680, 255100 · ICD-10 E71.3 · GARD 0017626
Start by learning the basics from an authoritative source, find a specialist or center that sees Multiple acyl-CoA dehydrogenase deficiency, severe neonatal 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 Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type, filtered to your area.
Tomeko shows live, recruiting studies for Multiple acyl-CoA dehydrogenase deficiency, severe neonatal type from ClinicalTrials.gov on the hub.